CA1153313A - Antiperspirant composition containing aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex and method of use - Google Patents
Antiperspirant composition containing aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex and method of useInfo
- Publication number
- CA1153313A CA1153313A CA000373677A CA373677A CA1153313A CA 1153313 A CA1153313 A CA 1153313A CA 000373677 A CA000373677 A CA 000373677A CA 373677 A CA373677 A CA 373677A CA 1153313 A CA1153313 A CA 1153313A
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- Prior art keywords
- aluminum
- glycine
- aluminum zirconium
- composition
- zirconium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/28—Zirconium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/58—Metal complex; Coordination compounds
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An antiperspirant composition buffered to a pH in the range of from about 2.5 to about 4.5 having incorporated therein as active ingredients a combination of aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex; an additionally added buffering agent, preferably glycine, may be incorporated in the composition.
An antiperspirant composition buffered to a pH in the range of from about 2.5 to about 4.5 having incorporated therein as active ingredients a combination of aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex; an additionally added buffering agent, preferably glycine, may be incorporated in the composition.
Description
~153313 ANTIPERSPIRANT COMPOSITION CONTAINING ALUMINUM
CHLOROHYDRATE, ALUMINUM CHLORIDE AND AN ALUMIN~M ZIRCONIUM
POLYCHLOR~HYDR~TE-CO~ EX AND METH~D OF USE
. . _ This invention relates to antiperspirant compositions.
More particularly, it concerns antiperspirant compositions having incorporated therein aluminum chlorohydrate, aluminum chloride, an aluminum zirconium polychlorohydrate complex and a buffering agent e.g. glycine.
Aluminum chlorhydrate (ACH) has been known for many years to be an effective and safe antiperspirant. Never-theless, there is room for improvement and the search to find more effective antiperspirant materials is constantly going on. It has also been known in the art for sometime that aluminum chloride and zirconium salts provide exceptionally effective antiperspirants. However, solutions of aluminum chloride hexahydrate and zirconium oxy- or hydroxychloride are very acidic and therefore, they are not widely used alone because of their irritation potential and high fabric damage. Therefore, various efforts have been centered on raising the pH to 3 to 4 by using less acidic aluminum salts and incorporating organic nitrogen containing compounds.
Daley (U.S. Patents 2,814,584 and 2,814,585) and Grad (U.S. Patent 2,854,382) showed that when zirconium oxy- or zirconium hydroxychloride are buffered with ACH
and glycine, the antiperspirant efficacy is greater than an ACH system alone. Since then, the combination of aluminum chlorohydrate, zirconium hydroxychloride and glycine has been used widely as a most effective antiperspirant active system.
Luedders et al in U.S. Patent 3,792,068 suggest a process for preparing an antiperspirant which comprises spray drying a solution containing, for example, ACH, zirconyl hydroxychloride and glycine. It is claimed that ~153313 this combination has superior characteristics not possessed when the components are dried separately and combined by simple physical mixing.
The British patent to Shin et al 1,347,950 discloses the use of a combination of ACH and aluminum chloride as an effective antiperspirant material. This combination was found to be particularly useful in an aerosol composition.
However, as in the case with other antiperspirant materials known in the prior art, it still left room for improvement.
Other antiperspirant systems containing aluminum and zirconium salts have been reported, for example, ~eekman (U.S. Patent 2,906,668), Rubino (U.S. Patents 3,97g,510;
3,981,896 and 4,017,599), Siegel et al (U.S. Patent 3,407,254), Mecca (U.S. Patent 3,g70,748), Shelton (U.S. Patent 4,202,879), etc. The antiperspirant activity of all these salts in these patents has not been clearly claimed as having superiority over systems containing æirconium hydroxychloride, ACH and glycine.
Although aluminum chloride, aluminum chlorohydrate, zirconyl hydroxychloride and certain aluminum zirconium chloro-hydrate complexes, individually have been suggested for use as antiperspirant materials in the prior art and the combination of aluminum chloride and aluminum chlorohydrate on the one hand, and the combination of aluminum chlorohydrate and zirconyl hydroxychloride on the other hand, have also been suggested for use as an active antiperspirant, it has been unexpectedly found that combination of aluminum chloride, aluminum chlorohydrate, an aluminum zirconium polychloro-hydrate complex as defined more particularly below act synergistically and at the same level of concentration of actives show a higher degree of antiperspirant activity than would be expected from the level of activity of the individual ingredients or certain combination of ingredients which are shown in the prior art. In combination with a buff-ering agent e.g. glycine, these materials provide a high ~ 53313 performance antiperspirant having a low potential for skin irritation and/or fabric damage.
It is accordingly an object of the present invention to provide highly effective antiperspirant compositions.
It is also an object of this invention to provide a process for inhibiting perspiration on the skin of individuals by application to the skin area the aforesaid antiperspirant compositions.
Other and more detailed objects of this invention will be apparent from the following description and claims.
In the following description, unless otherwise specified, the percentages are expressed as percentages by weight based on the total weight of the composition.
The aluminum chloride that is incorporated in the compo-sitions of the present invention may be aluminum chloride hydrated to various degrees. However, aluminum chloride hexahydrate (AlC13. 6H20) has been found to be most effect-ive and is therefore preferred for the purposes of the present invention.
The quantity of aluminum chloride that may be incor-porated in the present composition may vary somewhat.
Generally, the aluminum chloride will be incorporated in these compositions at a level of between about 0.5~ and about 6% by weight on an anhydrous basis based on the total weight of the composition. As the hexahydrate (AlC13. 6H20) it will be incorporated at a concentration of from about 0.9%
to about 11% by weight based on the total weight of the composition with the preferred range being from about 2%
to about 6% on the same basis.
The aluminum chloride hexahydrate will usually be incorporated in the present composition as a 50% a~ueous solution. When employed in this form, from about 1.8% to about 22% by weight of this composition based on the total ~;3313 weight of the composition will be used.
The aluminum chlorohydrate (sometimes referred to as aluminum chlorhydroxide) may also be incorporated in the composition of this invention in varying amounts. Usually, this will be used at a level in the range of from about 1%
to about 15~ by weight on an anhydrous basis based on the total weight of the composition with the preferred level falling in the range of from about 2% to about 10% by weight on the same weight basis. Aluminum chlorohydrate is also supplied as a 50% aqueous solution. When employed in this form, it will be used at a concentration of from 2.6~ to about 38% by weight based on the total weight of the com~osition.
to thls composition The ACH and aluminum chloride may be added~in whole or in part as a powdered mixture as described in the British patent to Shin et al 1,347,950. This may be prepared by drying an aqueous solution of aluminum chloride hexahydrate and ACH using conventional drying techniques such as oven drying, vacuum oven drying, spray drying or freeze drying. These compositions are characterized by the fact that the molar ratio of aluminum to chloride will fall within the range of from about 0.78:1 to about 1.95:1 with the preferred range being about 1.2:1 to about 1.5:1. When the molar ratio of aluminum to chloride is less than 1, the addition of larger amounts of buffering agent e.g. glycine may be necessary to reduce irritation potential and fabric damage.
The aluminum zirconium polychlorohydrate complexes that may be incorporated in the composition of the present invention may be described by the general formula:
(I) Alxzr(oH)yclz . nCH2COOH . mH2O
30wherein:
(a) x is a number from 2 to 10;
(b) Z is a number from 3 to 8;
.;
~53313 (c) y equals (3x + 4) - Z;
(d) the sum of y ~ Z is a number from 10 to 34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 y ordinarily will have a value of from about 5 to about 29.
As will be clear from Formula I, the glycine may be bound in the complex or it may be absent. The presence or absence of the glycine in the complex will determine the amount of unbound glycine or other buffer that may be incorporated in the composi-tion to increase the pH to a le~el of from about 2.5 to about 4~5 or the preferred pH of fr~m about 2.8 to about 3.8.
A number of aluminum zirconium polychlorohydrate com-plexes are known i~ the prior art which are useful for the present purposes. By way of example, the following may be mentioned along with their empirical formulas: aluminum zirconium tetrachlorohydrate (A14Zr(OH)12C14); aluminum zirconium tetrachlorohydrate glycine (Wickenol #E-369) ~A14Zr(OH)12C14 . NH2CH2COOH); aluminum zirconium trichloro-hydrate (A14Zr(OH)13C13; aluminum zirconium trichlorohydrate glycine (A14Zr(OH)13C13 . NH2CH2COOH); aluminum zirconium pentachlorohydrate (A110Zr(OH)29C15); aluminum zirconium pentachlorohydrate glycine (A110Zr(OH)29C15 . NH2CH2COOH);
aluminum zirconium octachlorohydrate (A16Zr(OH)14C18);
aluminum zirconium octachlorohydrate glycine (A16Zr(OH)14C18 .
NH2CH2COOH). The aluminum zirconium polychlorohydrate complex can be mixed individually with the ACH and AlC13 . 6H20 in solution or powder form or in various combinations thereof.
The OTC Panel on antiperspirants of the Food and 3~ Drug Administration has adopted certain nomenclature and specifications for various aluminum zirconium polychloro-hydrates that are useful in the present invention. These are set out in Table A below:
B * Trademark ~53313 Table A
Panel Adopted Metal-Halide Al/Zr Nomenclature Ratio Range Ratio Range Aluminum zirconium 2.1 down to but not 2.0 up to but not 5trichlorohydrate inc~udin~ 1.5:1 including 6.0:1 Aluminum zirconium 1.5 down to and 2.0 up to but not tetrachlorohydrate including 0.9:1 including 6.0:1 Aluminum zirconium 2.1 down to but not 6.0 up to and pentachlorohydrate including 1.5:1 including 10.0:1 10Aluminum zirconium 1.5 down to and 6 . o up to and octachlorohydrate including 0.9:1 including 10.0:1 A number of the aluminum zirconium polychlorohydrate complexes that are useful in the present invention are avail-able commerically~ Reheis Chemical Company promotes a series of materials under the general trademark REZALTM. The follow-ing Table describes a number of these products together with their specifications:
Table I
1 REZAL 36G Aluminum zirconium tetrachlorohydrex Gly (soln.)
CHLOROHYDRATE, ALUMINUM CHLORIDE AND AN ALUMIN~M ZIRCONIUM
POLYCHLOR~HYDR~TE-CO~ EX AND METH~D OF USE
. . _ This invention relates to antiperspirant compositions.
More particularly, it concerns antiperspirant compositions having incorporated therein aluminum chlorohydrate, aluminum chloride, an aluminum zirconium polychlorohydrate complex and a buffering agent e.g. glycine.
Aluminum chlorhydrate (ACH) has been known for many years to be an effective and safe antiperspirant. Never-theless, there is room for improvement and the search to find more effective antiperspirant materials is constantly going on. It has also been known in the art for sometime that aluminum chloride and zirconium salts provide exceptionally effective antiperspirants. However, solutions of aluminum chloride hexahydrate and zirconium oxy- or hydroxychloride are very acidic and therefore, they are not widely used alone because of their irritation potential and high fabric damage. Therefore, various efforts have been centered on raising the pH to 3 to 4 by using less acidic aluminum salts and incorporating organic nitrogen containing compounds.
Daley (U.S. Patents 2,814,584 and 2,814,585) and Grad (U.S. Patent 2,854,382) showed that when zirconium oxy- or zirconium hydroxychloride are buffered with ACH
and glycine, the antiperspirant efficacy is greater than an ACH system alone. Since then, the combination of aluminum chlorohydrate, zirconium hydroxychloride and glycine has been used widely as a most effective antiperspirant active system.
Luedders et al in U.S. Patent 3,792,068 suggest a process for preparing an antiperspirant which comprises spray drying a solution containing, for example, ACH, zirconyl hydroxychloride and glycine. It is claimed that ~153313 this combination has superior characteristics not possessed when the components are dried separately and combined by simple physical mixing.
The British patent to Shin et al 1,347,950 discloses the use of a combination of ACH and aluminum chloride as an effective antiperspirant material. This combination was found to be particularly useful in an aerosol composition.
However, as in the case with other antiperspirant materials known in the prior art, it still left room for improvement.
Other antiperspirant systems containing aluminum and zirconium salts have been reported, for example, ~eekman (U.S. Patent 2,906,668), Rubino (U.S. Patents 3,97g,510;
3,981,896 and 4,017,599), Siegel et al (U.S. Patent 3,407,254), Mecca (U.S. Patent 3,g70,748), Shelton (U.S. Patent 4,202,879), etc. The antiperspirant activity of all these salts in these patents has not been clearly claimed as having superiority over systems containing æirconium hydroxychloride, ACH and glycine.
Although aluminum chloride, aluminum chlorohydrate, zirconyl hydroxychloride and certain aluminum zirconium chloro-hydrate complexes, individually have been suggested for use as antiperspirant materials in the prior art and the combination of aluminum chloride and aluminum chlorohydrate on the one hand, and the combination of aluminum chlorohydrate and zirconyl hydroxychloride on the other hand, have also been suggested for use as an active antiperspirant, it has been unexpectedly found that combination of aluminum chloride, aluminum chlorohydrate, an aluminum zirconium polychloro-hydrate complex as defined more particularly below act synergistically and at the same level of concentration of actives show a higher degree of antiperspirant activity than would be expected from the level of activity of the individual ingredients or certain combination of ingredients which are shown in the prior art. In combination with a buff-ering agent e.g. glycine, these materials provide a high ~ 53313 performance antiperspirant having a low potential for skin irritation and/or fabric damage.
It is accordingly an object of the present invention to provide highly effective antiperspirant compositions.
It is also an object of this invention to provide a process for inhibiting perspiration on the skin of individuals by application to the skin area the aforesaid antiperspirant compositions.
Other and more detailed objects of this invention will be apparent from the following description and claims.
In the following description, unless otherwise specified, the percentages are expressed as percentages by weight based on the total weight of the composition.
The aluminum chloride that is incorporated in the compo-sitions of the present invention may be aluminum chloride hydrated to various degrees. However, aluminum chloride hexahydrate (AlC13. 6H20) has been found to be most effect-ive and is therefore preferred for the purposes of the present invention.
The quantity of aluminum chloride that may be incor-porated in the present composition may vary somewhat.
Generally, the aluminum chloride will be incorporated in these compositions at a level of between about 0.5~ and about 6% by weight on an anhydrous basis based on the total weight of the composition. As the hexahydrate (AlC13. 6H20) it will be incorporated at a concentration of from about 0.9%
to about 11% by weight based on the total weight of the composition with the preferred range being from about 2%
to about 6% on the same basis.
The aluminum chloride hexahydrate will usually be incorporated in the present composition as a 50% a~ueous solution. When employed in this form, from about 1.8% to about 22% by weight of this composition based on the total ~;3313 weight of the composition will be used.
The aluminum chlorohydrate (sometimes referred to as aluminum chlorhydroxide) may also be incorporated in the composition of this invention in varying amounts. Usually, this will be used at a level in the range of from about 1%
to about 15~ by weight on an anhydrous basis based on the total weight of the composition with the preferred level falling in the range of from about 2% to about 10% by weight on the same weight basis. Aluminum chlorohydrate is also supplied as a 50% aqueous solution. When employed in this form, it will be used at a concentration of from 2.6~ to about 38% by weight based on the total weight of the com~osition.
to thls composition The ACH and aluminum chloride may be added~in whole or in part as a powdered mixture as described in the British patent to Shin et al 1,347,950. This may be prepared by drying an aqueous solution of aluminum chloride hexahydrate and ACH using conventional drying techniques such as oven drying, vacuum oven drying, spray drying or freeze drying. These compositions are characterized by the fact that the molar ratio of aluminum to chloride will fall within the range of from about 0.78:1 to about 1.95:1 with the preferred range being about 1.2:1 to about 1.5:1. When the molar ratio of aluminum to chloride is less than 1, the addition of larger amounts of buffering agent e.g. glycine may be necessary to reduce irritation potential and fabric damage.
The aluminum zirconium polychlorohydrate complexes that may be incorporated in the composition of the present invention may be described by the general formula:
(I) Alxzr(oH)yclz . nCH2COOH . mH2O
30wherein:
(a) x is a number from 2 to 10;
(b) Z is a number from 3 to 8;
.;
~53313 (c) y equals (3x + 4) - Z;
(d) the sum of y ~ Z is a number from 10 to 34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 y ordinarily will have a value of from about 5 to about 29.
As will be clear from Formula I, the glycine may be bound in the complex or it may be absent. The presence or absence of the glycine in the complex will determine the amount of unbound glycine or other buffer that may be incorporated in the composi-tion to increase the pH to a le~el of from about 2.5 to about 4~5 or the preferred pH of fr~m about 2.8 to about 3.8.
A number of aluminum zirconium polychlorohydrate com-plexes are known i~ the prior art which are useful for the present purposes. By way of example, the following may be mentioned along with their empirical formulas: aluminum zirconium tetrachlorohydrate (A14Zr(OH)12C14); aluminum zirconium tetrachlorohydrate glycine (Wickenol #E-369) ~A14Zr(OH)12C14 . NH2CH2COOH); aluminum zirconium trichloro-hydrate (A14Zr(OH)13C13; aluminum zirconium trichlorohydrate glycine (A14Zr(OH)13C13 . NH2CH2COOH); aluminum zirconium pentachlorohydrate (A110Zr(OH)29C15); aluminum zirconium pentachlorohydrate glycine (A110Zr(OH)29C15 . NH2CH2COOH);
aluminum zirconium octachlorohydrate (A16Zr(OH)14C18);
aluminum zirconium octachlorohydrate glycine (A16Zr(OH)14C18 .
NH2CH2COOH). The aluminum zirconium polychlorohydrate complex can be mixed individually with the ACH and AlC13 . 6H20 in solution or powder form or in various combinations thereof.
The OTC Panel on antiperspirants of the Food and 3~ Drug Administration has adopted certain nomenclature and specifications for various aluminum zirconium polychloro-hydrates that are useful in the present invention. These are set out in Table A below:
B * Trademark ~53313 Table A
Panel Adopted Metal-Halide Al/Zr Nomenclature Ratio Range Ratio Range Aluminum zirconium 2.1 down to but not 2.0 up to but not 5trichlorohydrate inc~udin~ 1.5:1 including 6.0:1 Aluminum zirconium 1.5 down to and 2.0 up to but not tetrachlorohydrate including 0.9:1 including 6.0:1 Aluminum zirconium 2.1 down to but not 6.0 up to and pentachlorohydrate including 1.5:1 including 10.0:1 10Aluminum zirconium 1.5 down to and 6 . o up to and octachlorohydrate including 0.9:1 including 10.0:1 A number of the aluminum zirconium polychlorohydrate complexes that are useful in the present invention are avail-able commerically~ Reheis Chemical Company promotes a series of materials under the general trademark REZALTM. The follow-ing Table describes a number of these products together with their specifications:
Table I
1 REZAL 36G Aluminum zirconium tetrachlorohydrex Gly (soln.)
2 REZAL 36 Aluminum zirconium trichlorohydrate (pdr.)
3 REZAL 67 Aluminum zirconium pentachlorohydrate (soln.)
4 REZAL 67 Aluminum zirconium pentachlorohydrate (pdr.) .
Approx.
Al/Zr ratio 3.6:1 3.6:1 6.7:1 6.7:1 Approx.
metal/Cl ratio1.4:1 1.6:1 1.7:1 1.7:1 Concentration of solids ~ 35% 100% - 40% 100%
Aluminum(Al)5.0%-5.7%16.3%-17.7% 7.6%-8.4% 19.0%-21.0%
Zirconium(Zr)4.4%-5.7%13.8%-15.2%3.7%-4.3% 9.2%-10.8%
Glycine 3.6~-4.7~ --- --- ---Chloride(Cl)5.9%-6.7%16.0%-19.0% 6.5%-7.2% 16.2%-18.0%
Iron(Fe) NMT 50ppm NMT lOOppm NMT 50ppm NMT lOOppm Heavy metals (as Pb) NMT lOppm NMT 20ppm NMT lOppm NMT 20ppm Particle size (thru 325! mesh) --- ~ 97% min. --- ~97% min.
-' ~1533~3 Similar products are marketed by Wickhen Products, Inc. and the Comet Chemical Corporation.
The quantity of any aluminum zirconi~m polychlorohydrate comp~ex that will be incorporated in the composition of the present invention may also vary somewhat. Usually, it will be used at a concentration level in the range of from about
Approx.
Al/Zr ratio 3.6:1 3.6:1 6.7:1 6.7:1 Approx.
metal/Cl ratio1.4:1 1.6:1 1.7:1 1.7:1 Concentration of solids ~ 35% 100% - 40% 100%
Aluminum(Al)5.0%-5.7%16.3%-17.7% 7.6%-8.4% 19.0%-21.0%
Zirconium(Zr)4.4%-5.7%13.8%-15.2%3.7%-4.3% 9.2%-10.8%
Glycine 3.6~-4.7~ --- --- ---Chloride(Cl)5.9%-6.7%16.0%-19.0% 6.5%-7.2% 16.2%-18.0%
Iron(Fe) NMT 50ppm NMT lOOppm NMT 50ppm NMT lOOppm Heavy metals (as Pb) NMT lOppm NMT 20ppm NMT lOppm NMT 20ppm Particle size (thru 325! mesh) --- ~ 97% min. --- ~97% min.
-' ~1533~3 Similar products are marketed by Wickhen Products, Inc. and the Comet Chemical Corporation.
The quantity of any aluminum zirconi~m polychlorohydrate comp~ex that will be incorporated in the composition of the present invention may also vary somewhat. Usually, it will be used at a concentration level in the range of from about
5% to about 16% by weight on an anhydrous basis based on the total weight of the composition. In the preferred forms of this invention, the levels will be in the range of from about 8% to about 14% by weight on an anhydrous basis based on the total weight of the composition.
The aluminum zirconium polychlorohydrate complex of choice in the present invention is aluminum zirconium tetra-chlorohydrate glycine complex. This is usually used at a level of from about 5% to about 16% by weight on an anhydrous basis based on the total weight of the composition with the preferred level being in the range of from about 8% to about 14~ based on the same weight basis. The aluminum zirconium tetrachlorohydrate glycine complex is supplied as a 35%
aqueous solution. When employed in this form, it is usually incorporated in the present composition at a level in the range of from about 18% to about 60% by weight based on the total weight of the composition.
Glycine, the preferred buffering agent, is an important component of the present composition. This may be incorporated as free glycine or as part of the aluminum zirconium polychloro-hydrate complex or as a combination of the both. In general, the total ~lycine incorporated in these compositions (i.e.
as free glycine, complexed glycine or a combination of both) will fall in the range of from about 0.5% to about 5~ by weight based on the total weight of the composition. The preferred range of total glycine, however, is from about 1.5%
to about 3~ on the same weight basis.
Other buffering or complexing agents besides glycine can also be used in this invention. For example, other amino ~153313 acids or their salts (e.g. sodium glycinate, dihydroxy aluminum glycinate), urea, organic base containing nitrogen, metal hydroxide, carbonate, and oxide including alkaline and alkaline earth metal (Mg(OH)2, Na2C~3,ZnO, etc.). These buffering agents can be used alone or in combination with glycine to giYe the composition a pH
in the range of from 2.5 to 4.5 (preferably 2.8 to 3.8).
These complexing and bufferiny agents serve to reduce irritation potential and fabric damage. They also function to stabilize the antiperspirant system.
~ he compositions of the present invention may take a variety of dosage forms. Thus, they might be emulsion roll-on products or a clear hydro-alcoholic or aqueous roll-on products. Aqueous solutions of the aluminum chloride, ACH, aluminum zirconium polychlorohydrate complex and buffering agent e.g. glycine may be spray dried into an impalpable powder. This can be used as such or incorporated into sticks, suspensions, powders or roll-on products.
~ ~, 33i3 g _ Although the compositions of the present invention may take a variety of forms, they appear very effective in system that contain a relatively high water content. These may take the form of solution or emulsion ~n which the active ingredients (i.e. the aluminum chloride, ACH, aluminum zirconium polychloro-hydrate complex and buffer) are contained in the aqueous phase.
The aqueous emulsion systems are preferred since they give more organoleptically elegant compositions. ~hese emulsion systems will usually be of the oil-in-water type in which the active ingredients will be contained in the continuous aqueous phase.
The quantity of water that may be contained in these compositions may vary somewhat. Usually, it will comprise from about 40% to about 80% by weisht based on the total weight of the composition, the preferred range being from about 60% to about 75% on the same weight basis.
The emulsion type products of the present invention ~ -may also contain other ingredients that are commonly found in roll-on antiperspirant of the lotion or emulsion type.
These will include such things as emollients, surfactants, sequestering agents, perfumes, coloring agents, etc.
By way of illustrating the emollients that may be employed herein, mention may be made of fatty acid esters (isopropyl myristate , isopropyl palmitate);diesters of dicarboxylic acids (diisopropyl adipate), polyoxyalkylene glycol esters (polypropylene glycol 2000 monooleate); propylene glycol diesters of short chain fatty acids*(C8-C10)* (Neobee M-20);
polyoxypropylene fatty ethers (Procetyl, Arlamol E, Witconol APS, Witconol APM, etc.), propoxylated monohydric alcohol M.W. 880-930 (Fluid AP), fatty alcohol (hexadecyl alcohol), silicone oils (dimethyl po~siloxane, 10-2000 centistokes), cyclomethicones (volatile silicone 7207 and 7158-Unin Carbide), polyoxyethylene polyoxypropylene fatty ether (Procetyl AWS Modified, Witconol APES). Alone or mixtures of the above non-polar liquids are equally suitable for the purposes of this invention. Generally, the above emollients are organic oily liquids which are non-polar in character ~Trademarks ~S
and have ~a) a boiling point under atmospheric pressure not lower than about 120C; (b) a specific gravity between about 0.7 and 1.6, preferably between 0.7 and 1.2.
The quantity of emollient employed will vary somewhat, the level usually being within the range of from about 1 to about 30% by weight based on the total weight of the composition. Preferably, this will fall in the range of from about 2% to about 15% on the same weight basis.
A variety of surfactants and combinations of surfactants are also useful in preparing the present lotion or emulsion type products. These include such materials as generally nonionic, cationic and amphoteric surfactants which can be used in antiperspirant emulsion systems. Examples are as follows:
I. Nonionic Surfactants * *
1. Polyoxyethylene fatty ethers - Brij 30, Brij 35, * *
Brij 72, Brij 78, etc.
2. Polyoxypropylene polyoxyethylene fatty ethers -Procetyl AWS, Witconol APEM, Witconol APES, etc.
3. Polyoxyethylene alkyl phenyl ethers - Igepal*
CO 530, etc.
4. Polyoxyethylene sorbitan fatty acid esters -Tween*20, Tween*80, etc.
5. Sorbitan fatty acid esters - Span 60, Span 85, etc.
The aluminum zirconium polychlorohydrate complex of choice in the present invention is aluminum zirconium tetra-chlorohydrate glycine complex. This is usually used at a level of from about 5% to about 16% by weight on an anhydrous basis based on the total weight of the composition with the preferred level being in the range of from about 8% to about 14~ based on the same weight basis. The aluminum zirconium tetrachlorohydrate glycine complex is supplied as a 35%
aqueous solution. When employed in this form, it is usually incorporated in the present composition at a level in the range of from about 18% to about 60% by weight based on the total weight of the composition.
Glycine, the preferred buffering agent, is an important component of the present composition. This may be incorporated as free glycine or as part of the aluminum zirconium polychloro-hydrate complex or as a combination of the both. In general, the total ~lycine incorporated in these compositions (i.e.
as free glycine, complexed glycine or a combination of both) will fall in the range of from about 0.5% to about 5~ by weight based on the total weight of the composition. The preferred range of total glycine, however, is from about 1.5%
to about 3~ on the same weight basis.
Other buffering or complexing agents besides glycine can also be used in this invention. For example, other amino ~153313 acids or their salts (e.g. sodium glycinate, dihydroxy aluminum glycinate), urea, organic base containing nitrogen, metal hydroxide, carbonate, and oxide including alkaline and alkaline earth metal (Mg(OH)2, Na2C~3,ZnO, etc.). These buffering agents can be used alone or in combination with glycine to giYe the composition a pH
in the range of from 2.5 to 4.5 (preferably 2.8 to 3.8).
These complexing and bufferiny agents serve to reduce irritation potential and fabric damage. They also function to stabilize the antiperspirant system.
~ he compositions of the present invention may take a variety of dosage forms. Thus, they might be emulsion roll-on products or a clear hydro-alcoholic or aqueous roll-on products. Aqueous solutions of the aluminum chloride, ACH, aluminum zirconium polychlorohydrate complex and buffering agent e.g. glycine may be spray dried into an impalpable powder. This can be used as such or incorporated into sticks, suspensions, powders or roll-on products.
~ ~, 33i3 g _ Although the compositions of the present invention may take a variety of forms, they appear very effective in system that contain a relatively high water content. These may take the form of solution or emulsion ~n which the active ingredients (i.e. the aluminum chloride, ACH, aluminum zirconium polychloro-hydrate complex and buffer) are contained in the aqueous phase.
The aqueous emulsion systems are preferred since they give more organoleptically elegant compositions. ~hese emulsion systems will usually be of the oil-in-water type in which the active ingredients will be contained in the continuous aqueous phase.
The quantity of water that may be contained in these compositions may vary somewhat. Usually, it will comprise from about 40% to about 80% by weisht based on the total weight of the composition, the preferred range being from about 60% to about 75% on the same weight basis.
The emulsion type products of the present invention ~ -may also contain other ingredients that are commonly found in roll-on antiperspirant of the lotion or emulsion type.
These will include such things as emollients, surfactants, sequestering agents, perfumes, coloring agents, etc.
By way of illustrating the emollients that may be employed herein, mention may be made of fatty acid esters (isopropyl myristate , isopropyl palmitate);diesters of dicarboxylic acids (diisopropyl adipate), polyoxyalkylene glycol esters (polypropylene glycol 2000 monooleate); propylene glycol diesters of short chain fatty acids*(C8-C10)* (Neobee M-20);
polyoxypropylene fatty ethers (Procetyl, Arlamol E, Witconol APS, Witconol APM, etc.), propoxylated monohydric alcohol M.W. 880-930 (Fluid AP), fatty alcohol (hexadecyl alcohol), silicone oils (dimethyl po~siloxane, 10-2000 centistokes), cyclomethicones (volatile silicone 7207 and 7158-Unin Carbide), polyoxyethylene polyoxypropylene fatty ether (Procetyl AWS Modified, Witconol APES). Alone or mixtures of the above non-polar liquids are equally suitable for the purposes of this invention. Generally, the above emollients are organic oily liquids which are non-polar in character ~Trademarks ~S
and have ~a) a boiling point under atmospheric pressure not lower than about 120C; (b) a specific gravity between about 0.7 and 1.6, preferably between 0.7 and 1.2.
The quantity of emollient employed will vary somewhat, the level usually being within the range of from about 1 to about 30% by weight based on the total weight of the composition. Preferably, this will fall in the range of from about 2% to about 15% on the same weight basis.
A variety of surfactants and combinations of surfactants are also useful in preparing the present lotion or emulsion type products. These include such materials as generally nonionic, cationic and amphoteric surfactants which can be used in antiperspirant emulsion systems. Examples are as follows:
I. Nonionic Surfactants * *
1. Polyoxyethylene fatty ethers - Brij 30, Brij 35, * *
Brij 72, Brij 78, etc.
2. Polyoxypropylene polyoxyethylene fatty ethers -Procetyl AWS, Witconol APEM, Witconol APES, etc.
3. Polyoxyethylene alkyl phenyl ethers - Igepal*
CO 530, etc.
4. Polyoxyethylene sorbitan fatty acid esters -Tween*20, Tween*80, etc.
5. Sorbitan fatty acid esters - Span 60, Span 85, etc.
6. Lanolin ethers - Laneto 50, Solulan 98, etc.
7. Fatty alcohols a~d polyoxyethylene fatty ethers - Pro~ulgen G, Polawax, etc.
II. Cationic Surfactants N(Lauryl colamino formyl methyl)pyridinium chloride (Emcol*E607L) III. Amphoteric Surfactants Coconut imidazoline (Monateric CA-35%) IV. Auxiliary Surfactants 1. Glyceryl fatty acid esters - Glyceryl monostearate * Trademarks B
-- ~lS3313 2. Fatty acid amides - Witcamide 70 (Witco Chem. Co.) 3. Fatty alcohols - Stearyl alcohol As in the case with the emollients, the quantity employed can vary sQmewhat. For the most part, this will be in the range of from about 1% to about 10% by weight on an anhydrous basis based on the total weight of the composition with the preferred range being from about 2% to about 6% on the same weight basis.
As indicated above, one of the popular antiperspirant systems employed in the prior art is an aluminum zirconium trichlorohydrate glycine compleg . ~he present system has the following advantages over said popular system:
1. Low cost of goods. The above popular system is much more expensive than either AlC13 . 6H2O or ACH.
2. Better emulsion stability and more ease to manu-facture. Straight Al/Zr ~olychlorohydrate glyeine systems are difficult to stabilize and to manufacture as emulsions.
3. Low fabric staining potential. Generally~ straight Al/Zr polychlorohydrate glycine salts stain more than aluminum salts.
The following Examples are given to further illustrate the present invention. It is to be understood, however, that the invention is not limited thereto.
Formula 1908 Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 30 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.40 Aluminum chlorhydroxide, 50% 18.00 . "
.
.
~ ~1533~3 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP)-- 0.50 Aluminum zirconium tetrachloro-hydrex-glycine solution, 35% 35.00 Color FD&C Blue ~1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotiQn Color: Pale blue p~: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps . . . .
-Procedure:
1. In a suitable stainless steel kettle, melt together polyoxypropylene fatty alcohol ethers, polyoxyethylene(2)stearyl ether and polyoxyethylene(20)stearyl ether by heating to 140F.
Add the perfume and mix together just prior to Step 3.
2. In a separate stainless steel kettle, dissolve the disodium edetate in the water and heat to 140F.
3. Slowly add the oil phase to the water phase (both at 140F) using a Lightnin' mixer at slow agitation.
Maintain the temperature of 140F for 15 minutes.
4. At 140F, slowly add to the batch, using slow agitation, a solution consisting of the aluminum chlorhydroxide, aluminum chloride hexahydrate, glycine and aluminum zirconium tetrachlorohydrex-glycine solution which has been preheated to 120F. Continue agitation and cool the batch to 125F.
Mix for 15 minutes, maintaining the batch temperature at 120F-125F.
5. Cool the batch to 105F, add the dye solution and continue agitation and cooling.
6. When the batch temperature reaches 80-85F, stop agitation and adjust for water loss, if necessary.
, , 5l333~3 The composition and procedure of Example 1 is followed except that in place o the PPG-ll stearyl ether, Arlamol ESP
(PPG-15 stearyl ether~ is employed.
EX~MPLE 3 Formula 1956 Following the procedure of Example 1, the following composition is prepared:
_ngredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.32 Disodium edetate, dihydrate 0.10 Water, deionized 35.13 Butylated hydroxytoluene ~ 0.05 Aluminum chlorhydroxide, 50% 18.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35% 35.00 D&C Red #19 (0.1% Aq. Sol.) 0.08 D&C Yellow #10 (0.1% Aq. Sol.) 0.32 100. 00 Appearance: Smooth, opaque lotion Color: Pink pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps 1~3313 The composition and procedure of Example 3 is followed excepting that in place of the PPG-11 stear~l eth~r, Arlamol ESP
(PPG-15 Stearyl Ether) is used.
E ~MPLE 5 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients ~ by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 31.40 Aluminum chlorhydroxide, 50%12.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35%
45.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 ~ 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps The procedure and composition of Example 5 is followed excepting that in place of the PPG-ll stearyl ether, ~lamol ESP
(PPG-15 Stearyl Ether) is employed.
Formula 1979 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20~stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.40 Aluminum chlorhydroxide, 50% 15.50 Aluminum chloride hexahydrate solution, 50% 8.00 Aminoacetic acid (Glycine Crystal USP) ' 1 . 00 Aluminum zirconium tetrachlorohydrex-glycine solution, 35%
35.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-2000 cps The composition and procedure of Example 7 is followed excepting that in place of the PPG-lI stearyl ether, Arlamol ESP
(PPG-15 Stearyl Alcohol) is employed.
~, ,, -~ ~L153313 Formula 1991 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 31.40 Aluminum chlorhydroxide, 50% 10.00 Aluminum chloride hexahydrate solution, 50% 8.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-~lycine solution, 35%
45.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100. 00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 + 0.3 Viscosity: ~3 spindle at 20 RPM 15 seconds Overnight %iscosity: 500-1500 cps The composition and procedure of Example 9 is followed excepting that in place of the PPG~ll stearyl ether, Arlamol ESP
(PPG-15 Stearyl Ether) is employed.
~.~ .~
, :
~ 3313 Formula 1955 The procedure of Example 1 is followed and the following co~position is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether1.65 Polyoxyethylene(20)stearyl ether0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.60 Aluminum chlorhydroxide, 50% 18.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35~ 35.00 100 . 00 Appearance: Smooth, opaque lotion Color: White pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps The composition and procedure of Example 11 is followed excepting that in place of the PPG-ll stearyl ether, Arlamol ESP
(PPG-15 Stearyl Ether) is employed.
i3313 Formula BA 1810-64 Aluminum zirconium trichlorohydrate 31 powder was employed. The number following the term "trichlorohydrate"
in this and other Examples designates the Al/Zr molar ratio in the compound. Thus, for example, 31 designates an Al/Zr molar ratio of 3/1.
Primary Emulsion A % by Wt.
PPG-ll stearyl ether ~ 5.56 Polyoxyethylene(2)stearyl eth~r 4.07 Polyoxyethylene(20)stearyl ether 1.48 Perfume 0.74 Disodium edetate, dihydrate 0.25 FD&C Blue #1 (0.1% Aq. Sol.) 0.49 Water, deionized 87.41 100. 00 Ingredients % by Wt.
Al/Zr trichlorohydrate 31 powder10.00 ACH 50% solution 18.00 AlC13 . 6H20, 50% solution 6.00 Glycine 1.50 '~Jater, deionized 24.00 Primary Emulsion A q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps -` ~153313 Formula BA 18~0-65 Aluminum zirconium trichlorohydrate 21 powder (Al/Zr molar ratio = 2/1) was used:
Ingredients % by Wt.
Al/Zr trichlorohydrate 21 powder10.00 ACH 50~ solution 18.00 AlC13 . 6H2O ,50% solution 6.00 Glycine 1.50 Water, deionized 24.00 Primary Emulsion A q.s.-to 100.00 pH: 3.5 + 0.3 Overnight viscosity: 500-1500 cps Formula BA 1810-56 Aluminum zirconium octachlorohydrex-glycine powder 81 (Al/Zr molar ratio = 8/1) was used:
Ingredients% by Wt.
Al/Zr octachlorohydrex-glycine powder 81 15.00 ACH 50% solution10.00 AlC13 . 6H2O solution 8.00 Glycine 0.50 Water, deionized26.00 Primary Emulsion A q.s. to 100.00 pH: 3.2 + 0.3 Overnight viscosity: 500-1500 cps - ~153313 Formula BA 1810-57 Aluminum zirconium pentachlorohydrate solution (Al/Zr molar ratio = 10/1) was used:
Ingredients % by Wt.
Al/Zr pentachlorohydrate solution, 30~ 35.00 ACH 50% solution 10.00 AlC13 . 6H2O 50% solution 8.00 Glycine 2.00 Water, deionized 4.50 Primary Emulsion A q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 450-1500 cps Formula BQ 1856-83 Different buffering agent such as sodium carbonate is used as an additional buffering agent in this Example.
Primary Emulsion B % by Wt.
PPG-ll stearyl ether 6.43 Polyoxyethylene(2)stearyl ether 4.71 Polyoxyethylene(20)stearyl ether 1.71 Perfume 0.86 Disodium edetate, dihydrate 0.29 FD&C Blue #1 (0.1~ aq. sol.) 0.57 Water, deionized 85.43 100.00 ~ 53313 Ingredients % by Wt.
Al/Zr tetrachlorohydrex-glycine solution, 35% 45.00 ACH, 50% solution 10.00 AlC13 . 6H2O, 50% solution 8.00 Glycine 1.20 Sodium carbonate monohydrate 0.50 Water, deionized 0.30 Primary Emulsion B q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps Formula BQ 1856-83 Magnesium hydroxide was used as an additional buffering agent.
Ingredients % by Wt.
Al/Zr tetrachlorohydrex-glycine solution, 35~ 45.00 ACH, 50% solution 10.00 AlC13 . 6H2O, 50% solution 8.00 Glycine 0.50 Magnesium hydroxide 0.50 ~later, deionized 1.00 Primary Emulsion B q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps .,~,...
:
. .
-' ~lS33~3 Formula 1509-61 Ingredients % by Wt.
PPG-ll stearyl ether 2.25 5 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Water, deionized 41.20 Disodium edetate, dihydrate 0.10 DC Antifoam AF, 25% 0.10 Al/Zr tetrachlorohydrex-glycine solution, 35~ 35.00 15 ACH, 50% solution 15.00 AlC13 . 6H20, 50~ solution 3 . 00 Glycine 0.60 FD&C Blue #1 (0.1% aq. sol.) 0.20 100.00 pH: 3.4 + 0.3 overn~ght-vi~cosity; 400-1200 cps To demonstrate that the combination of aluminum chloride, ACH, aluminum zirconium polychlorohydrate and glycine act synergistically, a number of formulas identified in Table II
below were prepared. Formula ~ 1908 is representative of the present invention.
~ ' ~
.
~1~3313 ~ d ~ C~ H
O O Pl ~ 0 0 ~ 1~ ~
0 1- bn 1~ v~ m P ~ 0~ ~ ~ I t~ ~ oP I~ pJ ~ It 1~ o ~D O ~ (I
3 ~ ~ P X ~ X
- n ~ ~ 3 ~n ~ ~ 1- ~ 1--~ ~ ~ ~ ~ O~
m ~:
I~ ~ P t ~ ~ ~ ~n ~ ~ ~ O ~ S~ O O ~S
(D u~ O 1~ O
O P
o ~ ^ ~ tn O
o o ~
~S tn CO 1~ #
o o . . . I I I . I_ ~ (- ~O O ~ Ul CO O O 1-- ~ ~ CO I I #
. . . . . . . . I I i-CO ~ I_ ~ ~n o co ~ a~
a~
o~
p~ ~
I_ ~ ~ H
1~ O O i~ 1 :~-.. . . . . .. . . #
~n ~ 9 W ~I Ul I_ 1'- v~
ul ~n ~9 ~ pl O
CO r~
O
_ 1--CO O ~ ~ ~ ~ ~ ~ #
. - . . . . I 1-o ~ I~ ~ w n o I o ~ ~
H ~1 ~ _ DI O O
~_~ O ~ (D C~ ~ I_ ~D~v 1'- P I ~ ~P W I ~
. 1~ t I I O It ~S O tD Pl I ~ I I
_ p~
v~ ~ W Y
P P~ p p C~ ~ ~ P
G~ P l'~ ~n ~
p ~ < --O' ~ t tD Ul o ~ ~
~C
-' ~1533~3 As will be noted, each of these formulas is similar excepting for the active ingredients that are employed.
Further, each contains the total active ingredients at essentially the same concentration i.e. about 18% on an anhydrous basis.
Each of these compositions was tested for antiper-spirant activity. The general procedure employed was as described in Federal Register, Vol. 43, Number 196, October 10, 1978. It is called the gravimetric axillary antiperspirant test. Paired comparison (treated vs.
treated) studies of the antiperspirant effectiveness of antiperspirant emulsion.
The details of the test procedure are given below.
Test Procedure A random test pattern supplied by Statistical Services is employed, e.g. if one test material is evaluated, half of the panelists receives the test material under the left axilla while the remaining half receives it under the right.
The opposite axilla serves as a control. If two test materials are evaluated, half the panel has product A
applied to the left axilla and product B to the right while the remaining panelists have the reverse product/axilla allocations.
The test is conducted during a five-day period (~onday through Friday). Sweating is induced under environ-mental conditions of 100F ~ 2 and 40% relative humidity + 2%.
Day 1: Control measurement followed by product application Panelists wait one-half hour at room temperature (approximately 65-80F) after which time they enter the test room. They then place the untared Webril Pads (which are folded in half to a size of 4"x2") in their axillae.
Subj~ects sit in the test room for a 40 minute warm-up period.
At the end of this period, the warm-up pads are removed by the panelists and are discarded.
~53313 The panelists remove the plastic bags containing the tared collection pads from the manila envelopes. The subjects insert the pads as directed by a technician.
The pads remain in the axilla for a period of 20 minutes.
After such time, the panelists are instructed to remove the pads and to place them into the designated plastic bags which are then returned to the manila envelopes.
The panelists exit the test room, hand in their envelopes, and then wash their axillae with tepid water with the aid of gauze pads and towel dry them. Approximately one to three minutes later, the test material is applied and the panelists leave. The plastic bags are removed from the manila envelopes and are weighed by a technician.
Panelists must perspire at least 200 mg/axilla to continue participation on the panel.
Day 2: Product application only Panelists wait one-half hour at room temperature, after which time they wash their axillae with tepid water with the aid of gauze pads and towel dry them. Approximately one to three minutes later, the test material is applied and the panelists leave.
Day 3: Product application and collection Panelists wait one-half hour at room temperature, after which time they wash their axillae as described above.
Approximately one to five minutes later the test material is applied. The panelists then wait one hour at room tempera-ture. Then they enter the test room for a 40-minute warm-up and place the untared pads in their axillae. At the end of this period, the warm-up pads are removed and discarded.
The panelists remove the plastic bags containing the tared collection pads from the manila envelopes. They insert the pads as directed by a technician. The pads remain in the axillae for a period of 20 minutes. Then the panelists are instructed to remove the pads and to place them into the .
designated plastic bags which are then returned to the manila envelopes. The panelists exit the test room, hand in their envelopes, and leave. The plastic bags are removed from the manila envelopes and are weighed by a technician.
Day 4: Product application only Same as Day 2.
Day 5 : Product application and collection Same as Day 3.
The results of the test are summarized as follows:
I. Formula #1908 vs. Formula #1052 Results:
The data from this study, employing 47 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicated that Antiperspirant Roll-on Formula #1908 was significantly more effective than Formula #1052 at the 0.01 level.
This conclusion is supported by the A/B ratio (amount ofsweat collected from A treated axilla over B treated axilla) for thé final treatment-collection day (adjusted by control) averaging 0.819 which is significantly different from 1.0 equality.
The above data indicates that Formula #1908 is about 18% more effective than Formula #1052.
II. Formula #1908 vs. Formula #1676 Results:
The data from this study, employing 46 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicated that Formula #1908 was significantly more effective than Formula #1676 at the 0.01 level.
~;33~3 This conclusion ~s supported by the A/B ratio for the final treatment-collection day (adjusted for control) averaging 0.883 which is significantly different from 1.0 e~uality.
The above data indicates that Formula #1908 is about 12% more effective than Formula #1676.
III. Formula #1908 vs. Commercial Emulsion Roll-On Formula # BR 4504 _ _ -Results~
The data from-this study, employing 48 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicates that Formula #1908 was significantly more effective than Commercial Emulsion Roll-On at the 0.01 level.
This conclusion is supported by the A/B ratio for the final treatment-collection day (adjusted for control) averaging 0.881 which is significantly different from 1.0 equality.
The above data indicates that Formula #1908 is about 12%
more effective than Formula #BR 4504.
IV. Formula #1341 (see Table II ) which contains as anti-perspirant actives a combination of ACH and AlC13 . 6H2O
(at a level of about 18.2) in a similar manner was shown to be on the average 9.6% less effective than the Commercial Emulsion Roll-on (BR 4504) which contains 19.7% Al/Zr tri-chlorohydrate as the ~ntiperspirant active (see Table II).
The latter, however, has also been shown to be less effective than Formula #1908 embodied in the present invention i.e.
Formula #1908 was about 12% more effective than Fo~mula #BR 4505 (see Paragraph III~.
;33't 3 V. Formula #1991 (See Example 9) in a similar manner was shown to be 15% more effective than a commercial suspension roll-on product identified as Formula #BR 4751. The latter has the following composition:
Formula # BR 4751 Ingredients % by Wt.
Aluminum zirconium tetrachloro-hydrate (anhydrous basis) 13.8 Glycine 2.0 Bentone 38 3.25 Cyclomethicone and Perfume q.s. to 100.00 Although the invention has been described with reference to specific forms thereof, it will be understood that many changes and modifications may be made without departing from the spirit of this invention.
II. Cationic Surfactants N(Lauryl colamino formyl methyl)pyridinium chloride (Emcol*E607L) III. Amphoteric Surfactants Coconut imidazoline (Monateric CA-35%) IV. Auxiliary Surfactants 1. Glyceryl fatty acid esters - Glyceryl monostearate * Trademarks B
-- ~lS3313 2. Fatty acid amides - Witcamide 70 (Witco Chem. Co.) 3. Fatty alcohols - Stearyl alcohol As in the case with the emollients, the quantity employed can vary sQmewhat. For the most part, this will be in the range of from about 1% to about 10% by weight on an anhydrous basis based on the total weight of the composition with the preferred range being from about 2% to about 6% on the same weight basis.
As indicated above, one of the popular antiperspirant systems employed in the prior art is an aluminum zirconium trichlorohydrate glycine compleg . ~he present system has the following advantages over said popular system:
1. Low cost of goods. The above popular system is much more expensive than either AlC13 . 6H2O or ACH.
2. Better emulsion stability and more ease to manu-facture. Straight Al/Zr ~olychlorohydrate glyeine systems are difficult to stabilize and to manufacture as emulsions.
3. Low fabric staining potential. Generally~ straight Al/Zr polychlorohydrate glycine salts stain more than aluminum salts.
The following Examples are given to further illustrate the present invention. It is to be understood, however, that the invention is not limited thereto.
Formula 1908 Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 30 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.40 Aluminum chlorhydroxide, 50% 18.00 . "
.
.
~ ~1533~3 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP)-- 0.50 Aluminum zirconium tetrachloro-hydrex-glycine solution, 35% 35.00 Color FD&C Blue ~1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotiQn Color: Pale blue p~: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps . . . .
-Procedure:
1. In a suitable stainless steel kettle, melt together polyoxypropylene fatty alcohol ethers, polyoxyethylene(2)stearyl ether and polyoxyethylene(20)stearyl ether by heating to 140F.
Add the perfume and mix together just prior to Step 3.
2. In a separate stainless steel kettle, dissolve the disodium edetate in the water and heat to 140F.
3. Slowly add the oil phase to the water phase (both at 140F) using a Lightnin' mixer at slow agitation.
Maintain the temperature of 140F for 15 minutes.
4. At 140F, slowly add to the batch, using slow agitation, a solution consisting of the aluminum chlorhydroxide, aluminum chloride hexahydrate, glycine and aluminum zirconium tetrachlorohydrex-glycine solution which has been preheated to 120F. Continue agitation and cool the batch to 125F.
Mix for 15 minutes, maintaining the batch temperature at 120F-125F.
5. Cool the batch to 105F, add the dye solution and continue agitation and cooling.
6. When the batch temperature reaches 80-85F, stop agitation and adjust for water loss, if necessary.
, , 5l333~3 The composition and procedure of Example 1 is followed except that in place o the PPG-ll stearyl ether, Arlamol ESP
(PPG-15 stearyl ether~ is employed.
EX~MPLE 3 Formula 1956 Following the procedure of Example 1, the following composition is prepared:
_ngredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.32 Disodium edetate, dihydrate 0.10 Water, deionized 35.13 Butylated hydroxytoluene ~ 0.05 Aluminum chlorhydroxide, 50% 18.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35% 35.00 D&C Red #19 (0.1% Aq. Sol.) 0.08 D&C Yellow #10 (0.1% Aq. Sol.) 0.32 100. 00 Appearance: Smooth, opaque lotion Color: Pink pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps 1~3313 The composition and procedure of Example 3 is followed excepting that in place of the PPG-11 stear~l eth~r, Arlamol ESP
(PPG-15 Stearyl Ether) is used.
E ~MPLE 5 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients ~ by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 31.40 Aluminum chlorhydroxide, 50%12.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35%
45.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 ~ 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps The procedure and composition of Example 5 is followed excepting that in place of the PPG-ll stearyl ether, ~lamol ESP
(PPG-15 Stearyl Ether) is employed.
Formula 1979 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20~stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.40 Aluminum chlorhydroxide, 50% 15.50 Aluminum chloride hexahydrate solution, 50% 8.00 Aminoacetic acid (Glycine Crystal USP) ' 1 . 00 Aluminum zirconium tetrachlorohydrex-glycine solution, 35%
35.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100.00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-2000 cps The composition and procedure of Example 7 is followed excepting that in place of the PPG-lI stearyl ether, Arlamol ESP
(PPG-15 Stearyl Alcohol) is employed.
~, ,, -~ ~L153313 Formula 1991 The procedure of Example 1 is followed and the following composition is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 31.40 Aluminum chlorhydroxide, 50% 10.00 Aluminum chloride hexahydrate solution, 50% 8.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-~lycine solution, 35%
45.00 FD&C Blue #1 (0.1% Aq. Sol.) 0.20 100. 00 Appearance: Smooth, opaque lotion Color: Pale blue pH: 3.3 + 0.3 Viscosity: ~3 spindle at 20 RPM 15 seconds Overnight %iscosity: 500-1500 cps The composition and procedure of Example 9 is followed excepting that in place of the PPG~ll stearyl ether, Arlamol ESP
(PPG-15 Stearyl Ether) is employed.
~.~ .~
, :
~ 3313 Formula 1955 The procedure of Example 1 is followed and the following co~position is prepared:
Ingredients % by Wt.
PPG-ll stearyl ether 2.25 Polyoxyethylene(2)stearyl ether1.65 Polyoxyethylene(20)stearyl ether0.60 Perfume 0.30 Disodium edetate, dihydrate 0.10 Water, deionized 35.60 Aluminum chlorhydroxide, 50% 18.00 Aluminum chloride hexahydrate solution, 50% 6.00 Aminoacetic acid (Glycine Crystal USP) 0.50 Aluminum zirconium tetrachlorohydrex-glycine solution, 35~ 35.00 100 . 00 Appearance: Smooth, opaque lotion Color: White pH: 3.3 + 0.3 Viscosity: #3 spindle at 20 RPM 15 seconds Overnight viscosity: 500-1500 cps The composition and procedure of Example 11 is followed excepting that in place of the PPG-ll stearyl ether, Arlamol ESP
(PPG-15 Stearyl Ether) is employed.
i3313 Formula BA 1810-64 Aluminum zirconium trichlorohydrate 31 powder was employed. The number following the term "trichlorohydrate"
in this and other Examples designates the Al/Zr molar ratio in the compound. Thus, for example, 31 designates an Al/Zr molar ratio of 3/1.
Primary Emulsion A % by Wt.
PPG-ll stearyl ether ~ 5.56 Polyoxyethylene(2)stearyl eth~r 4.07 Polyoxyethylene(20)stearyl ether 1.48 Perfume 0.74 Disodium edetate, dihydrate 0.25 FD&C Blue #1 (0.1% Aq. Sol.) 0.49 Water, deionized 87.41 100. 00 Ingredients % by Wt.
Al/Zr trichlorohydrate 31 powder10.00 ACH 50% solution 18.00 AlC13 . 6H20, 50% solution 6.00 Glycine 1.50 '~Jater, deionized 24.00 Primary Emulsion A q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps -` ~153313 Formula BA 18~0-65 Aluminum zirconium trichlorohydrate 21 powder (Al/Zr molar ratio = 2/1) was used:
Ingredients % by Wt.
Al/Zr trichlorohydrate 21 powder10.00 ACH 50~ solution 18.00 AlC13 . 6H2O ,50% solution 6.00 Glycine 1.50 Water, deionized 24.00 Primary Emulsion A q.s.-to 100.00 pH: 3.5 + 0.3 Overnight viscosity: 500-1500 cps Formula BA 1810-56 Aluminum zirconium octachlorohydrex-glycine powder 81 (Al/Zr molar ratio = 8/1) was used:
Ingredients% by Wt.
Al/Zr octachlorohydrex-glycine powder 81 15.00 ACH 50% solution10.00 AlC13 . 6H2O solution 8.00 Glycine 0.50 Water, deionized26.00 Primary Emulsion A q.s. to 100.00 pH: 3.2 + 0.3 Overnight viscosity: 500-1500 cps - ~153313 Formula BA 1810-57 Aluminum zirconium pentachlorohydrate solution (Al/Zr molar ratio = 10/1) was used:
Ingredients % by Wt.
Al/Zr pentachlorohydrate solution, 30~ 35.00 ACH 50% solution 10.00 AlC13 . 6H2O 50% solution 8.00 Glycine 2.00 Water, deionized 4.50 Primary Emulsion A q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 450-1500 cps Formula BQ 1856-83 Different buffering agent such as sodium carbonate is used as an additional buffering agent in this Example.
Primary Emulsion B % by Wt.
PPG-ll stearyl ether 6.43 Polyoxyethylene(2)stearyl ether 4.71 Polyoxyethylene(20)stearyl ether 1.71 Perfume 0.86 Disodium edetate, dihydrate 0.29 FD&C Blue #1 (0.1~ aq. sol.) 0.57 Water, deionized 85.43 100.00 ~ 53313 Ingredients % by Wt.
Al/Zr tetrachlorohydrex-glycine solution, 35% 45.00 ACH, 50% solution 10.00 AlC13 . 6H2O, 50% solution 8.00 Glycine 1.20 Sodium carbonate monohydrate 0.50 Water, deionized 0.30 Primary Emulsion B q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps Formula BQ 1856-83 Magnesium hydroxide was used as an additional buffering agent.
Ingredients % by Wt.
Al/Zr tetrachlorohydrex-glycine solution, 35~ 45.00 ACH, 50% solution 10.00 AlC13 . 6H2O, 50% solution 8.00 Glycine 0.50 Magnesium hydroxide 0.50 ~later, deionized 1.00 Primary Emulsion B q.s. to 100.00 pH: 3.4 + 0.3 Overnight viscosity: 500-1500 cps .,~,...
:
. .
-' ~lS33~3 Formula 1509-61 Ingredients % by Wt.
PPG-ll stearyl ether 2.25 5 Polyoxyethylene(2)stearyl ether 1.65 Polyoxyethylene(20)stearyl ether 0.60 Perfume 0.30 Water, deionized 41.20 Disodium edetate, dihydrate 0.10 DC Antifoam AF, 25% 0.10 Al/Zr tetrachlorohydrex-glycine solution, 35~ 35.00 15 ACH, 50% solution 15.00 AlC13 . 6H20, 50~ solution 3 . 00 Glycine 0.60 FD&C Blue #1 (0.1% aq. sol.) 0.20 100.00 pH: 3.4 + 0.3 overn~ght-vi~cosity; 400-1200 cps To demonstrate that the combination of aluminum chloride, ACH, aluminum zirconium polychlorohydrate and glycine act synergistically, a number of formulas identified in Table II
below were prepared. Formula ~ 1908 is representative of the present invention.
~ ' ~
.
~1~3313 ~ d ~ C~ H
O O Pl ~ 0 0 ~ 1~ ~
0 1- bn 1~ v~ m P ~ 0~ ~ ~ I t~ ~ oP I~ pJ ~ It 1~ o ~D O ~ (I
3 ~ ~ P X ~ X
- n ~ ~ 3 ~n ~ ~ 1- ~ 1--~ ~ ~ ~ ~ O~
m ~:
I~ ~ P t ~ ~ ~ ~n ~ ~ ~ O ~ S~ O O ~S
(D u~ O 1~ O
O P
o ~ ^ ~ tn O
o o ~
~S tn CO 1~ #
o o . . . I I I . I_ ~ (- ~O O ~ Ul CO O O 1-- ~ ~ CO I I #
. . . . . . . . I I i-CO ~ I_ ~ ~n o co ~ a~
a~
o~
p~ ~
I_ ~ ~ H
1~ O O i~ 1 :~-.. . . . . .. . . #
~n ~ 9 W ~I Ul I_ 1'- v~
ul ~n ~9 ~ pl O
CO r~
O
_ 1--CO O ~ ~ ~ ~ ~ ~ #
. - . . . . I 1-o ~ I~ ~ w n o I o ~ ~
H ~1 ~ _ DI O O
~_~ O ~ (D C~ ~ I_ ~D~v 1'- P I ~ ~P W I ~
. 1~ t I I O It ~S O tD Pl I ~ I I
_ p~
v~ ~ W Y
P P~ p p C~ ~ ~ P
G~ P l'~ ~n ~
p ~ < --O' ~ t tD Ul o ~ ~
~C
-' ~1533~3 As will be noted, each of these formulas is similar excepting for the active ingredients that are employed.
Further, each contains the total active ingredients at essentially the same concentration i.e. about 18% on an anhydrous basis.
Each of these compositions was tested for antiper-spirant activity. The general procedure employed was as described in Federal Register, Vol. 43, Number 196, October 10, 1978. It is called the gravimetric axillary antiperspirant test. Paired comparison (treated vs.
treated) studies of the antiperspirant effectiveness of antiperspirant emulsion.
The details of the test procedure are given below.
Test Procedure A random test pattern supplied by Statistical Services is employed, e.g. if one test material is evaluated, half of the panelists receives the test material under the left axilla while the remaining half receives it under the right.
The opposite axilla serves as a control. If two test materials are evaluated, half the panel has product A
applied to the left axilla and product B to the right while the remaining panelists have the reverse product/axilla allocations.
The test is conducted during a five-day period (~onday through Friday). Sweating is induced under environ-mental conditions of 100F ~ 2 and 40% relative humidity + 2%.
Day 1: Control measurement followed by product application Panelists wait one-half hour at room temperature (approximately 65-80F) after which time they enter the test room. They then place the untared Webril Pads (which are folded in half to a size of 4"x2") in their axillae.
Subj~ects sit in the test room for a 40 minute warm-up period.
At the end of this period, the warm-up pads are removed by the panelists and are discarded.
~53313 The panelists remove the plastic bags containing the tared collection pads from the manila envelopes. The subjects insert the pads as directed by a technician.
The pads remain in the axilla for a period of 20 minutes.
After such time, the panelists are instructed to remove the pads and to place them into the designated plastic bags which are then returned to the manila envelopes.
The panelists exit the test room, hand in their envelopes, and then wash their axillae with tepid water with the aid of gauze pads and towel dry them. Approximately one to three minutes later, the test material is applied and the panelists leave. The plastic bags are removed from the manila envelopes and are weighed by a technician.
Panelists must perspire at least 200 mg/axilla to continue participation on the panel.
Day 2: Product application only Panelists wait one-half hour at room temperature, after which time they wash their axillae with tepid water with the aid of gauze pads and towel dry them. Approximately one to three minutes later, the test material is applied and the panelists leave.
Day 3: Product application and collection Panelists wait one-half hour at room temperature, after which time they wash their axillae as described above.
Approximately one to five minutes later the test material is applied. The panelists then wait one hour at room tempera-ture. Then they enter the test room for a 40-minute warm-up and place the untared pads in their axillae. At the end of this period, the warm-up pads are removed and discarded.
The panelists remove the plastic bags containing the tared collection pads from the manila envelopes. They insert the pads as directed by a technician. The pads remain in the axillae for a period of 20 minutes. Then the panelists are instructed to remove the pads and to place them into the .
designated plastic bags which are then returned to the manila envelopes. The panelists exit the test room, hand in their envelopes, and leave. The plastic bags are removed from the manila envelopes and are weighed by a technician.
Day 4: Product application only Same as Day 2.
Day 5 : Product application and collection Same as Day 3.
The results of the test are summarized as follows:
I. Formula #1908 vs. Formula #1052 Results:
The data from this study, employing 47 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicated that Antiperspirant Roll-on Formula #1908 was significantly more effective than Formula #1052 at the 0.01 level.
This conclusion is supported by the A/B ratio (amount ofsweat collected from A treated axilla over B treated axilla) for thé final treatment-collection day (adjusted by control) averaging 0.819 which is significantly different from 1.0 equality.
The above data indicates that Formula #1908 is about 18% more effective than Formula #1052.
II. Formula #1908 vs. Formula #1676 Results:
The data from this study, employing 46 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicated that Formula #1908 was significantly more effective than Formula #1676 at the 0.01 level.
~;33~3 This conclusion ~s supported by the A/B ratio for the final treatment-collection day (adjusted for control) averaging 0.883 which is significantly different from 1.0 e~uality.
The above data indicates that Formula #1908 is about 12% more effective than Formula #1676.
III. Formula #1908 vs. Commercial Emulsion Roll-On Formula # BR 4504 _ _ -Results~
The data from-this study, employing 48 female subjects, were submitted to the Statistical Services Department for evaluation.
Briefly, their analysis indicates that Formula #1908 was significantly more effective than Commercial Emulsion Roll-On at the 0.01 level.
This conclusion is supported by the A/B ratio for the final treatment-collection day (adjusted for control) averaging 0.881 which is significantly different from 1.0 equality.
The above data indicates that Formula #1908 is about 12%
more effective than Formula #BR 4504.
IV. Formula #1341 (see Table II ) which contains as anti-perspirant actives a combination of ACH and AlC13 . 6H2O
(at a level of about 18.2) in a similar manner was shown to be on the average 9.6% less effective than the Commercial Emulsion Roll-on (BR 4504) which contains 19.7% Al/Zr tri-chlorohydrate as the ~ntiperspirant active (see Table II).
The latter, however, has also been shown to be less effective than Formula #1908 embodied in the present invention i.e.
Formula #1908 was about 12% more effective than Fo~mula #BR 4505 (see Paragraph III~.
;33't 3 V. Formula #1991 (See Example 9) in a similar manner was shown to be 15% more effective than a commercial suspension roll-on product identified as Formula #BR 4751. The latter has the following composition:
Formula # BR 4751 Ingredients % by Wt.
Aluminum zirconium tetrachloro-hydrate (anhydrous basis) 13.8 Glycine 2.0 Bentone 38 3.25 Cyclomethicone and Perfume q.s. to 100.00 Although the invention has been described with reference to specific forms thereof, it will be understood that many changes and modifications may be made without departing from the spirit of this invention.
Claims (14)
1. An antiperspirant composition buffered to a pH in the range of from about 2.5 to about 4.5, said composition having incorporated therein as active ingredients aluminum chloride, aluminum chlorohydrate, and an aluminum zirconium polychlorohydrate complex, said aluminum zirconium polychlorohydrate complex having the formula:
(I) wherein:
(a) x is a number from 2 to 10;
(b) z is a number from 3 to 8;
(c) y equals (3x + 4) - Z;
(d) the sum of y + Z is a number from 10 to.34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 said active ingredients being incorporated in said composition in the following weight percentages based on the total weight of said composition and on an anhydrous basis:
(1) aluminum chloride from about 0.5% to about 6%
(2) aluminum chlorohydrate from about 1% to about 15%
(3) aluminum zirconium polychlorohydrate complex from about 5% to about 16%.
(I) wherein:
(a) x is a number from 2 to 10;
(b) z is a number from 3 to 8;
(c) y equals (3x + 4) - Z;
(d) the sum of y + Z is a number from 10 to.34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 said active ingredients being incorporated in said composition in the following weight percentages based on the total weight of said composition and on an anhydrous basis:
(1) aluminum chloride from about 0.5% to about 6%
(2) aluminum chlorohydrate from about 1% to about 15%
(3) aluminum zirconium polychlorohydrate complex from about 5% to about 16%.
2. A composition according to Claim 1 including an additionally added buffering agent.
3. A composition according to Claim 2 in which the additionally added buffering agent is glycine.
4. A composition according to Claim 3 in which the total amount of glycine in bound and/or unbound form is present in said composition at a level in the range of from about 0.5% to about 5% by weight based on the total weight of the composition.
5. A composition according to Claim 1 wherein the aluminum chloride is incorporated as the aluminum chloride hexahydrate.
6. A composition according to Claim 1 in which the aluminum zirconium polychlorohydrate complex is aluminum zirconium tetrachlorohydrate glycine.
7. A composition according to Claim 1 wherein the aluminum zirconium polychlorohydrate complex is selected from the group consisting of aluminum zirconium tetrachloro-hydrate, aluminum zirconium tetrachlorohydrate glycine;
aluminum zirconium trichlorohydrate; aluminum zirconium trichlorohydrate glycine; aluminum zirconium pentachloro-hydrate; aluminum zirconium pentachlorohydrate glycine;
aluminum zirconium octachlorohydrate; aluminum zirconium octachlorohydrate glycine and mixtures thereof.
aluminum zirconium trichlorohydrate; aluminum zirconium trichlorohydrate glycine; aluminum zirconium pentachloro-hydrate; aluminum zirconium pentachlorohydrate glycine;
aluminum zirconium octachlorohydrate; aluminum zirconium octachlorohydrate glycine and mixtures thereof.
8. A composition according to Claim 7 wherein the aluminum chloride is incorporated as the hexahydrate.
9. An antiperspirant composition buffered to a pH in the range of from about 2.8 to 3.8, said composi-tion having incorporated therein as active ingredients aluminum chloride, aluminum chlorohydrate, an aluminum zirconium polychlorohydrate complex and containing glycine, said aluminum zirconium polychlorohydrate complex having the formula:
(I) wherein:
(a) x is a number from 2 to 10;
(b) Z is a number from.3 to 8;
(c) y equals (3x + 4) - Z;
(d) the sum of y + Z is a number from 10 to 34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 said active ingredients being incorporated in said composition in the following weight percentages based on the total weight of said composition and on an anhydrous basis:
(1) aluminum chloride from about 1.5% to about 3.3%
(2) aluminum chlorohydxate from about 2% to about 10%
(3) aluminum zirconium polychlorohydrate complex from about 8% to about 14%
the total ueight percent of glycine in bound and/or unbound form being from about 1.5% to about 3% based on the total weight of the composition.
(I) wherein:
(a) x is a number from 2 to 10;
(b) Z is a number from.3 to 8;
(c) y equals (3x + 4) - Z;
(d) the sum of y + Z is a number from 10 to 34;
(e) m is a number from 0 to 12;
(f) n is a number from 0 to 3 said active ingredients being incorporated in said composition in the following weight percentages based on the total weight of said composition and on an anhydrous basis:
(1) aluminum chloride from about 1.5% to about 3.3%
(2) aluminum chlorohydxate from about 2% to about 10%
(3) aluminum zirconium polychlorohydrate complex from about 8% to about 14%
the total ueight percent of glycine in bound and/or unbound form being from about 1.5% to about 3% based on the total weight of the composition.
10. A composition according to Claim 9 wherein the aluminum chloride is incorporated as the aluminum chloride hexahydrate.
11. A composition according to Claim 10 in which the aluminum zirconium polychlorohydrate complex is aluminum zirconium tetrachlorohydrate glycine.
12. A composition according to Claim 10 wherein the aluminum zirconium polychlorohydrate complex is selected from the group consisting of aluminum zirconium tetrachlorohydrate; aluminum zirconium tetrachlorohydrate glycine; aluminum zirconium trichlorohydrate; aluminum zirconium trichlorohydrate glycine; aluminum zirconium pentachlorohydrate; aluminum zirconium pentachlorohydrate glycine; aluminum zirconium octachlorohydrate; aluminum zirconium octachlorohydrate glycine and mixtures thereof.
13. A composition according to Claim 12 wherein the aluminum chloride is incorporated as the hexahydrate.
14. A composition according to Claims 1, 2 or 3, in the form of a oil-in-water emulsion in which at least a large component of the active ingredients and the glycine are contained in the water phase.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21641380A | 1980-12-15 | 1980-12-15 | |
| US216,413 | 1980-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1153313A true CA1153313A (en) | 1983-09-06 |
Family
ID=22806970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000373677A Expired CA1153313A (en) | 1980-12-15 | 1981-03-23 | Antiperspirant composition containing aluminum chlorohydrate, aluminum chloride and an aluminum zirconium polychlorohydrate complex and method of use |
Country Status (15)
| Country | Link |
|---|---|
| JP (1) | JPS57131715A (en) |
| AU (1) | AU547985B2 (en) |
| BE (1) | BE891488A (en) |
| CA (1) | CA1153313A (en) |
| CH (1) | CH649707A5 (en) |
| DE (1) | DE3149649A1 (en) |
| ES (1) | ES507961A0 (en) |
| FR (1) | FR2495933A1 (en) |
| GB (1) | GB2091099B (en) |
| GR (1) | GR76682B (en) |
| IT (1) | IT1172144B (en) |
| NZ (1) | NZ198966A (en) |
| PT (1) | PT74127B (en) |
| SE (1) | SE452108B (en) |
| ZA (1) | ZA817173B (en) |
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| US6375937B1 (en) | 2000-10-20 | 2002-04-23 | Colgate-Palmolive Company | Antiperspirant salts for enhanced cosmetic products |
| US6649152B2 (en) | 2000-10-25 | 2003-11-18 | The Gillette Company | Aluminum-zirconium antiperspirant salts with high peak 5 Al content |
| US6663854B1 (en) | 2002-06-19 | 2003-12-16 | Yan-Fei Shen | Aluminum-zirconium antiperspirant salts made with zirconium salts having low Zr:Cl ratio |
| US6726901B2 (en) | 2002-05-09 | 2004-04-27 | The Gillette Company | Stabilized antiperspirant compositions containing aluminum-zirconium salts with low M:Cl ratio |
| US7311898B2 (en) | 2002-12-09 | 2007-12-25 | Colgate-Palmolive Company | High efficacy, low irritation aluminum salts and related products |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5589196A (en) * | 1983-08-16 | 1996-12-31 | The Gillette Company | Antiperspirant composition |
| US4775528A (en) * | 1983-08-16 | 1988-10-04 | The Gillette Company | Antiperspirant composition |
| NZ241567A (en) * | 1991-02-13 | 1994-08-26 | Bristol Myers Squibb Co | Zirconium-aluminium-amino acid salts, and antiperspirant compositions thereof |
| CA2082561A1 (en) * | 1991-11-12 | 1993-05-13 | Francis J. Leng | Antiperspirant materials and compositions |
| US6042816A (en) * | 1998-08-19 | 2000-03-28 | The Gillette Company | Enhanced antiperspirant salts stabilized with calcium and concentrated aqueous solutions of such salts |
| AU772448B2 (en) | 2000-01-18 | 2004-04-29 | Unilever Plc | Anti-microbial antiperspirant products |
| JP7009088B2 (en) * | 2017-06-07 | 2022-01-25 | ライオン株式会社 | Antiperspirant composition |
| AU2022306468A1 (en) * | 2021-07-07 | 2023-12-14 | Unilever Global Ip Limited | Method of manufacture of antiperspirant salts |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA958338A (en) * | 1971-03-08 | 1974-11-26 | Chung T. Shin | Antiperspirant powder aerosol compositions containing aluminum chloride and water soluble aluminum compounds and methods of preparation |
| US4049792A (en) * | 1973-06-26 | 1977-09-20 | The Procter & Gamble Company | Antiperspirant stick |
| DE2608123B2 (en) * | 1975-03-12 | 1981-07-23 | Colgate-Palmolive Co., 10022 New York, N.Y. | Antiperspirant in aerosol form |
| US4083956A (en) * | 1976-04-29 | 1978-04-11 | The Procter & Gamble Company | Anhydrous antiperspirant creams |
| US4120948A (en) * | 1976-11-29 | 1978-10-17 | The Procter & Gamble Company | Two phase antiperspirant compositions |
| CA1140470A (en) * | 1980-05-27 | 1983-02-01 | Leonard Mackles | Aluminum chloride and aluminum zirconium hydroxychloride as antiperspirant |
-
1981
- 1981-03-23 CA CA000373677A patent/CA1153313A/en not_active Expired
- 1981-10-16 ZA ZA817173A patent/ZA817173B/en unknown
- 1981-10-16 AU AU76533/81A patent/AU547985B2/en not_active Ceased
- 1981-11-13 NZ NZ198966A patent/NZ198966A/en unknown
- 1981-11-27 GR GR66635A patent/GR76682B/el unknown
- 1981-12-10 IT IT49876/81A patent/IT1172144B/en active
- 1981-12-11 JP JP56198733A patent/JPS57131715A/en active Granted
- 1981-12-11 FR FR8123189A patent/FR2495933A1/en active Granted
- 1981-12-14 GB GB8137597A patent/GB2091099B/en not_active Expired
- 1981-12-14 ES ES507961A patent/ES507961A0/en active Granted
- 1981-12-14 CH CH7981/81A patent/CH649707A5/en not_active IP Right Cessation
- 1981-12-14 PT PT74127A patent/PT74127B/en unknown
- 1981-12-15 SE SE8107512A patent/SE452108B/en not_active IP Right Cessation
- 1981-12-15 DE DE19813149649 patent/DE3149649A1/en active Granted
- 1981-12-15 BE BE0/206844A patent/BE891488A/en not_active IP Right Cessation
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6375937B1 (en) | 2000-10-20 | 2002-04-23 | Colgate-Palmolive Company | Antiperspirant salts for enhanced cosmetic products |
| US6649152B2 (en) | 2000-10-25 | 2003-11-18 | The Gillette Company | Aluminum-zirconium antiperspirant salts with high peak 5 Al content |
| US6726901B2 (en) | 2002-05-09 | 2004-04-27 | The Gillette Company | Stabilized antiperspirant compositions containing aluminum-zirconium salts with low M:Cl ratio |
| US6663854B1 (en) | 2002-06-19 | 2003-12-16 | Yan-Fei Shen | Aluminum-zirconium antiperspirant salts made with zirconium salts having low Zr:Cl ratio |
| US7311898B2 (en) | 2002-12-09 | 2007-12-25 | Colgate-Palmolive Company | High efficacy, low irritation aluminum salts and related products |
Also Published As
| Publication number | Publication date |
|---|---|
| AU547985B2 (en) | 1985-11-14 |
| SE452108B (en) | 1987-11-16 |
| IT1172144B (en) | 1987-06-18 |
| GB2091099B (en) | 1985-05-01 |
| AU7653381A (en) | 1982-08-12 |
| FR2495933A1 (en) | 1982-06-18 |
| BE891488A (en) | 1982-06-15 |
| GB2091099A (en) | 1982-07-28 |
| DE3149649C2 (en) | 1991-08-08 |
| DE3149649A1 (en) | 1982-09-02 |
| ES8303085A1 (en) | 1983-02-01 |
| NZ198966A (en) | 1985-04-30 |
| SE8107512L (en) | 1982-06-16 |
| ES507961A0 (en) | 1983-02-01 |
| ZA817173B (en) | 1982-10-27 |
| FR2495933B1 (en) | 1985-04-19 |
| PT74127A (en) | 1982-01-01 |
| PT74127B (en) | 1984-01-05 |
| JPS57131715A (en) | 1982-08-14 |
| JPH0239486B2 (en) | 1990-09-05 |
| GR76682B (en) | 1984-08-24 |
| CH649707A5 (en) | 1985-06-14 |
| IT8149876A0 (en) | 1981-12-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |