EP1647591A1 - Formulation claire de nettoyage - Google Patents
Formulation claire de nettoyage Download PDFInfo
- Publication number
- EP1647591A1 EP1647591A1 EP05027073A EP05027073A EP1647591A1 EP 1647591 A1 EP1647591 A1 EP 1647591A1 EP 05027073 A EP05027073 A EP 05027073A EP 05027073 A EP05027073 A EP 05027073A EP 1647591 A1 EP1647591 A1 EP 1647591A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight percent
- alkyl
- acrylate copolymer
- cationic polymer
- added
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or non-ionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0013—Liquid compositions with insoluble particles in suspension
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/14—Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
Definitions
- the invention relates to a shower gel formulation.
- shower gel formulations which are mild to the skin are well known in the art.
- Such a formulation may optionally contain skin feel agents, such as cationic polymers.
- skin feel agents such as cationic polymers.
- anionic surfactants when one desires to suspend particulates and/or beads in the formulation, frequently substantial quantities of anionic surfactants have been incorporated, and provide clear solutions. Unfortunately, the addition of such anionic surfactants diminishes the mildness of the shower gel formulation.
- U.S. Patent No. 5,656,257 discloses an anionic shampoo and conditioning composition comprising an oily conditioning agent, a shampooing agent, and an acrylate copolymer, a cationic conditioning agent and water.
- the acrylate copolymer is used to suspend the anionic shampooing and cationic conditioning agent and prevent it then from inactivating one another.
- U.S. Patent No. 5,656,257 does not, however, disclose a clear, mild cleansing composition containing a combination of surfactant types, which is capable of suspending beads or other insoluble particulates or gas bubbles.
- the present invention comprises a shower gel formulation having a clear appearance and which suspends beads (e.g. agar/TiO2/sunflower oil beads), insoluble particles and gas bubbles while having one or more acrylate copolymers, a betaine or other amphoteric surfactant and a cationic polymer (e.g. guar) present in the formulation.
- beads e.g. agar/TiO2/sunflower oil beads
- insoluble particles and gas bubbles while having one or more acrylate copolymers, a betaine or other amphoteric surfactant and a cationic polymer (e.g. guar) present in the formulation.
- anionic acrylates i.e. Aculyn type acrylates (available from ISP)
- anionic polymers are generally considered to be incompatible with cationic charged ingredients.
- polymeric cationics, as well as some large, bulky quaternary materials, can possibly be incorporated in formulations containing such acrylates.
- the optimum order of addition in these instances generally requires the acrylate to be neutralised with a base prior to the addition of any cationics.
- Clarity or transparency is herein defined as having a turbidity less than or equal to 105 NTU (Nephelometric Turbidity Units).
- amphoteric surfactants such as betaine (which is also cationic in nature and not a true amphoteric), may be optionally added to the inventive formulation in the range of 0.01 - 15 weight percent, preferably 1-10 weight percent to increase mildness without creating noticeable haziness.
- Prior art shower gels that suspend beads or particulate matter are primarily composed of anionic surfactant and structurant which in most cases are harsher than the inventive formula.
- the present invention provides an aqueous, clear shower gel which is capable of suspension, comprising:
- the present invention provides an aqueous, clear cleansing gel that is capable of suspending insoluble material or gas bubbles, comprising:
- the present invention provides an aqueous, clear cleansing gel which is capable of suspending insoluble material or gas bubbles, comprising:
- Acrylate polymers and copolymers which are useful in the invention include one or more copolymers containing at least one monomer selected from the group consisting of methacrylic acid, acrylic acid, amino acrylic acid, an acrylic acid ester of a C8 -30 alkyl, alkylaryl, aryl, heterocyclic, alkoxyl, alkoxyl alkyl ester of a C8-30 alkyl or alkenyl; either substituted or unsubstituted; a methacrylic acid ester of a C8 -C30 alkyl, alkylaryl, aryl, heterocyclic, alkoxyl, alkoxyl alkyl ester of a C8-30 alkyl, or alkenyl; either substituted or unsubstituted; a C1-4 alkyl acrylate, and a C1-4 methacrylate; either substituted or unsubstituted, and the like.
- Other useful acrylate polymers and copolymers are disclosed in U.S. Patent
- Preferred acrylate polymers include the following INCI named materials: acrylates/c12-24 pareth-25 acrylate copolymer, obtainable as Synthalen® W2000 from 3V Inc. (Wehawken, NJ); acrylates/steareth-20 methacrylate copolymer obtainable as Aculyn® 22 from International Specialty Products Corp. (Lombard, IL); and acrylates copolymer obtainable as either Aculyn® 33 from International Specialty Products Corp. or as Polymer EX-518® from BF Goodrich Corp.
- inventive compositions may be used for the cleansing of the user's skin and hair and is applied to a surface (e.g. a skin surface) via topical applications to release or deposit an effective amount of the transparent composition to perform the desired cleansing function.
- the frequency of topical application can vary widely, depending on the user's need. With respect to personal application to the skin, such application can range from about once per day to about four times per day, preferably from about twice a day to about three times a day.
- compositions of these shower gels are summarised in Tables 1 and 2.
- the processing methods used to prepare these compositions listed in Table 1 are provided below:
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to 73.8°C (165°F). The temperature was maintained at 73.8°C (165°F). Agitation of the center turbine was increased as was the wall sweep so that there was a slight vortex.
- Acrylate copolymer was added to the tank and mixed.
- the anionic surfactants were then added to the tank and mixed, and then the amphoteric surfactant was added and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and was mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank. Then the glycerin was added.
- the preservative was added and at 40.6°C (105 °F) the fragrance was added and mixed well.
- the mixture was then cooled to 35°C (95 °F).
- 35°C (95 °F) the viscosity was measured and adjusted with ammonium sulfate to the desired viscosity.
- the insoluble components were added and mixed gently. The mixture was then cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.3°C (165°F). The agitation of the center turbine and the wall sweep was increased so that there was a slight vortex. Tetrasodium EDTA was added to the tank and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the anionic surfactants were added and mixed. Next the amphoteric surfactants were added and mixed, and then the acrylate copolymer was added and mixed.
- the composition was then mixed for 30 minutes at 73.8°C (165°F), and was then cooled to 35°C (95 °F). At 46.1°C (115 °F), the preservative was added and mixed well. At 35°C (95 °F), the pH was measured and adjusted with citric acid to clarity within a target pH range of 5.5 to 7.0. At 35°C (95 °F), the viscosity was measured and adjusted if necessary to the desired viscosity. The insoluble components were then added and mixed, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- the acrylate copolymer was added to the tank and mixed.
- the anionic surfactant was added and mixed. Agitation was decreased and the amphoteric surfactant added and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the remaining acrylate copolymer was premixed with water to a dilution of 4.5 to 1 and added to the tank and mixed with gentle agitation.
- the batch was mixed for 30 minutes at 73.8°C (165°F) and was started to be cooled to 35°C (95 °F).
- the glycerin was added, at 46.1°C (115 °F), the preservative and then the UV inhibitor were added.
- the EDTA and the EHDP were added and at 40.6°C (105 °F), the fragrance was added and mixed.
- the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity. The insoluble components were then added and mixed gently, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 46.1°C (115°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- Preservative was added to the tank and mixed.
- the acrylate copolymer was added to the tank slowly and mixed for 5 minutes.
- the anionic surfactants were added, then the amphoteric surfactants and mixed.
- the batch was cooled to 35°C (95 °F).
- the pH was measured and adjusted with an alkaline pH adjuster to a target pH range of 5.5 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity.
- the insoluble components were added and mixed, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- the acrylate copolymer was added to the tank and mixed.
- the anionic surfactant was then added and mixed. Agitation was decreased, and the amphoteric surfactant added and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the remaining acrylate copolymer was premixed with water to a dilution of 4.5 to 1, added to the tank and mixed with gentle agitation.
- the batch was mixed for 30 minutes at 73.8°C (165°F), and then started to cool to 35°C (95 °F).
- the glycerin was added, at 46.1°C (115 °F) the preservative and then the UV inhibitor were added.
- the EDTA and the EHDP were added and mixed.
- the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity.
- the insoluble components were then added and mixed gently, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex. Tetrasodium EDTA was added to the tank.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank. Agitation was decreased, and the acrylate copolymer(s) added and mixed. The anionic surfactants were added to the tank and mixed. The amphoteric surfactant was added next and mixed.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex. Tetrasodium EDTA was added to the tank and then subsequently the acrylate copolymer(s). The anionic surfactants were then added to the tank and mixed. The amphoteric surfactant was added next and mixed. The cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- the acrylate copolymer was added to the tank and mixed.
- the anionic surfactant was added and mixed. Agitation was decreased and the amphoteric surfactant added and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the remaining acrylate copolymer was premixed with water to a dilution of 4.5 to 1 and added to the tank and mixed with gentle agitation.
- the batch was mixed for 30 minutes at 73.8°C (165°F) and cooled to 35°C (95 °F).
- the glycerin was added, and at 46.1°C (115 °F) the preservative and then the UV inhibitor were added.
- the EDTA and the EHDP were added and mix.
- the fragrance was added and mixed well.
- the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity. The insoluble components were added and mix, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there is a slight vortex.
- the acrylate copolymer was added to the tank and mixed.
- the anionic surfactant was added and mixed. Agitation was decreased, and the amphoteric surfactant added and mix.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the remaining acrylate copolymer was premixed with water to a dilution of 4.5 to 1 and added to the tank and mixed with gentle agitation.
- the batch was mixed for 30 minutes at 73.8°C (165°F) and was then cooled to 35°C (95 °F).
- the preservative was added, and at 40.6°C (105 °F) the fragrance was added and mixed.
- 35°C (95 °F) the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity.
- the insoluble components were added and mixed gently, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- EDTA was added to the tank and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the anionic surfactant was added and mixed.
- the amphoteric surfactant was added and mixed.
- the acrylate copolymer was added to the tank and mixed.
- the agitation was decreased and the batch mixed for 30 minutes at 73.8°C (165°F) and then cooled to 35°C (95 °F).
- the preservative was added and mixed.
- the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity. The insoluble components were added and mixed, and the composition cooled to room temperature.
- the initial distilled water charge was added to a center turbine tank with wall scrape agitation and heated to and maintained at 73.8°C (165°F). Agitation of the center turbine and the wall sweep was increased so that there was a slight vortex.
- EDTA and then the acrylate copolymers were added to the tank and mixed.
- the anionic surfactant was added and mixed.
- the amphoteric surfactant was added and mixed.
- the cationic polymer was premixed with propylene glycol if the cationic polymer was a solid, and mixed well with no lumps. If the cationic polymer was a liquid, it was added straight to the tank.
- the agitation was decreased and the batch mixed for 30 minutes at 73.8°C (165°F), and then cooled to 35°C (95 °F).
- the preservative was and mixed.
- the pH was measured and adjusted with an alkaline pH adjuster to clarity within a target pH range of 5.9 to 7.0.
- the viscosity was measured and adjusted with propylene glycol to the desired viscosity. The insoluble components were added and mixed, and the composition cooled to room temperature.
- Anionic surfactant e.g. Sodium Laureth Sulfate (3EO) About 10-20 Betaine (e.g. Cocoamidopropyl betaine) About 2-15 Acrylate Copolymer (e.g. Aculyn 33 and 22) About 2 - 15 Silicone (e.g. Dimethicone Copolyol Sulfosuccinate About 0.1 - 5 Fragrance About 0 - 1.0 Cationic surfactant (e.g.
- Hydroxypropyl Guar Hydroxypropyl Trimonium Chloride About .05 - 5 Propylene Glycol About 0.1 - 2.0 Preservative About 0.1 - 2.0 Sodium Hydroxide to adjust pH to 6.0 to 7.0 Beads (e.g. Agar/ Titanium Dioxide/Sunflower Oil Beads About 0.1 - 2.0 Water q.s. to 100
- viscosity is measured using conventional techniques with a Brookfield viscometer, Model HBDVII+ CP, spindle No. 41 at 0.5 rpm at 25°C.
- the acceptability of formulation clarity was measured qualitatively and quantitively using a visual method of turbidity determination and a turbidimeter respectively.
- the visual method involves looking through a determined path length of the formulation to a visual target and determining if the visual target is legible or recognizable. This target may be a straight line, a set of parallel lines, or a number or letter printed on white paper.
- the test formulation was placed in a glass beaker such that the height from the bottom of the beaker to the top surface of the formulation was 10.16 cm (four inches). The formulation is made free of air bubbles. A piece of paper with the visual target is placed under the beaker.
- the assessor looked through the top surface of the formulation to the visual target. If the visual target appeared similar to the original, the formulation is of acceptable clarity and receives a 'pass' rating. If the visual target appeared significantly hazy, or is out of focus compared to the original target, the formulation is of unacceptable clarity and receives a 'fail' rating.
- Turbidity was quantitatively determined by a Turbidimeter, Model DRT-100D, manufactured by Shaban Manufacturing Inc, H. F. Instruments Division using a sample cuvette of 28 mm diameter by 91 mm in length with a flat bottom. Samples that had received a 'pass' rating from the visual method were found to have a turbidity measurement of less than or equal to 105 NTU's (Nephelometric Turbidity Units). Samples that had received a 'fail' rating from the visual method were found to have a turbidity measurement of greater than 105 NTU's.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15335599P | 1999-09-10 | 1999-09-10 | |
EP00960513A EP1210402B1 (fr) | 1999-09-10 | 2000-08-23 | Formulation de nettoyage et de suspension claire |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00960513A Division EP1210402B1 (fr) | 1999-09-10 | 2000-08-23 | Formulation de nettoyage et de suspension claire |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1647591A1 true EP1647591A1 (fr) | 2006-04-19 |
Family
ID=36091509
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05027073A Withdrawn EP1647591A1 (fr) | 1999-09-10 | 2000-08-23 | Formulation claire de nettoyage |
Country Status (1)
Country | Link |
---|---|
EP (1) | EP1647591A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011098802A1 (fr) * | 2010-02-12 | 2011-08-18 | Reckitt Benckiser N.V. | Composition |
WO2021069126A1 (fr) | 2019-10-11 | 2021-04-15 | Beiersdorf Ag | Préparation de nettoyage contenant de la gomme de caesalpinia spinosa |
CN112716815A (zh) * | 2020-11-18 | 2021-04-30 | 苏州绿叶日用品有限公司 | 一种具有悬浮能力的清洁剂组合物 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2283754A (en) * | 1993-11-11 | 1995-05-17 | Procter & Gamble | Liquid personal cleansing composition |
US5656257A (en) * | 1995-04-28 | 1997-08-12 | Electronics Hair Styling, Inc. | Shampoo and conditioning composition |
WO1998013022A1 (fr) * | 1996-09-24 | 1998-04-02 | Unilever Plc | Compositions liquides comprenant des tensioactifs ameliorant la stabilite et procede d'amelioration de la stabilite a basse temperature de ces compositions |
WO1999036054A1 (fr) * | 1998-01-19 | 1999-07-22 | Rhodia Chimie | Utilisation, dans les compositions cosmetiques, d'agents tensioactifs amphoteres pour precipiter, a la dilution, des polymeres cationiques |
-
2000
- 2000-08-23 EP EP05027073A patent/EP1647591A1/fr not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2283754A (en) * | 1993-11-11 | 1995-05-17 | Procter & Gamble | Liquid personal cleansing composition |
US5656257A (en) * | 1995-04-28 | 1997-08-12 | Electronics Hair Styling, Inc. | Shampoo and conditioning composition |
WO1998013022A1 (fr) * | 1996-09-24 | 1998-04-02 | Unilever Plc | Compositions liquides comprenant des tensioactifs ameliorant la stabilite et procede d'amelioration de la stabilite a basse temperature de ces compositions |
WO1999036054A1 (fr) * | 1998-01-19 | 1999-07-22 | Rhodia Chimie | Utilisation, dans les compositions cosmetiques, d'agents tensioactifs amphoteres pour precipiter, a la dilution, des polymeres cationiques |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011098802A1 (fr) * | 2010-02-12 | 2011-08-18 | Reckitt Benckiser N.V. | Composition |
AU2011214128B2 (en) * | 2010-02-12 | 2014-05-29 | Reckitt Benckiser Vanish B.V. | Composition |
US8759273B2 (en) | 2010-02-12 | 2014-06-24 | Reckitt Benckiser N.V. | Thickening composition comprising a copolymer of polydiallyldimethylammonium chloride and acrylamide |
RU2559335C2 (ru) * | 2010-02-12 | 2015-08-10 | Рекитт Бенкизер Н.В. | Композиция |
WO2021069126A1 (fr) | 2019-10-11 | 2021-04-15 | Beiersdorf Ag | Préparation de nettoyage contenant de la gomme de caesalpinia spinosa |
CN112716815A (zh) * | 2020-11-18 | 2021-04-30 | 苏州绿叶日用品有限公司 | 一种具有悬浮能力的清洁剂组合物 |
CN112716815B (zh) * | 2020-11-18 | 2024-03-29 | 苏州绿叶日用品有限公司 | 一种具有悬浮能力的清洁剂组合物 |
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