GB818361A - Detergent preparations for the hair - Google Patents

Detergent preparations for the hair

Info

Publication number
GB818361A
GB818361A GB20893/55A GB2089355A GB818361A GB 818361 A GB818361 A GB 818361A GB 20893/55 A GB20893/55 A GB 20893/55A GB 2089355 A GB2089355 A GB 2089355A GB 818361 A GB818361 A GB 818361A
Authority
GB
United Kingdom
Prior art keywords
acid
ethylene diamine
hydroxyethyl
amide
fatty acid
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.)
Expired
Application number
GB20893/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Schweiz AG
Original Assignee
Ciba AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ciba AG filed Critical Ciba AG
Publication of GB818361A publication Critical patent/GB818361A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur

Landscapes

  • 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)
  • Cosmetics (AREA)

Abstract

Cation-active shampoo preparations comprise (a) at least one compound which is free from imidazoline rings containing one or more basic nitrogen atoms, and also at least one nonaromatic residue of more than 6 carbon atoms, in the form of a water-soluble salt, including a quaternary ammonium salt, and (b) a non-ionic condensation product of tertiary dodecyl mercaptan and an alkaline oxide, preferably ethylene oxide and, if desired, (c) a compound of the kind used as an addition to detergent preparations for the hair; (a) may be the lactate of triethanolamine mono-coconut acid ester; the reaction product of coconut fatty acid amide, paraformaldehyde, triethanolamine and sodium carbonate; the lactate of the reaction product of coconut fatty acid with a condensate of monoethanolamine and propylene oxide; the sodium salts of the reaction products of N - hydroxyethyl - N1 - lauroyl - ethylene diamine with glycerol a -chlorhydrin, with chloracetamide, or with mono-chloracetic acid; sodium salts of the reaction products of N-hydroxyethyl - N1 - stearoyl ethylene diamine with glycerol a -chlorhydrin, or with monochloracetic acid; lauramido-ethyl-pyridinium sulphate; the lauryl or coconut acid ester of N : N - dimethylethanolamine hydrochloride; the lauryl ester of triethanolamine hydrochloride; octadecyl pyridinium bromide; dimethyl - octadecyl - hydroxyethyl - ammonium chloride; stearamidoethylene - trimethyl ammonium methosulphate; p - (stearylamino)-phenyl - trimethyl - ammonium methosulphate; or the lactate of the amide of mono-or tri - hydroxyethyl - ethylene diamine with lauric or stearic acid. The detailed preparation of most of the compounds is supplied (see Group IV (b)); (c) comprises such substances as primary phosphates, glycollic acid, citric acid, and especially lactic acid. Perfumes, dyes, bleaching and thickening agents, and fatty acid alkanolamides, for example, coconut fatty acid ethanolamide, may also be added, and the compositions may be produced in solid, paste, or liquid form. specifications 815,784 and 818,362 are referred to.ALSO:Additives for hair-washing preparations (see Group III) are prepared as follows: (1) ethylene diamine is reacted with ethylene oxide at 65-100 DEG C. to form N : N : N1-trihydroxyethyl-ethylene diamine which is amidified by reaction with lauric acid at 110-140 DEG C. in vacuo; (2) coconut oil fatty acid amide is heated with paraformaldehyde and triethanolamine in the presence of sodium carbonate at 60-85 DEG C. and then further heated in the presence of boric acid under reduced pressure; (3) mono ethanolamine is reacted with propylene oxide (4 mols.) at 110-130 DEG C. and the product is then esterified with coconut oil fatty acid by heating firstly at 140 DEG C. and finally at 170-175 DEG C. under reduced pressure; the lactate of the ester is mentioned; (4) hydroxyethyl-ethylene diamine is heated at the boil with lauric acid in xylene and in the presence of boric acid to give an amide; the product may be reacted with glycerol monochlorhydrin or chlor-acetamide by refluxing in ethanol, or with chloracetic acid at 80 DEG C. in water, thereafter treating with NaOH; (5) stearic acid is heated with hydroxyethyl ethylene diamine in boiling xylene in the presence of boric acid; the resulting amide may be reacted with chloracetamide, ethylene chlorhydrin or glycerol mono-chlorhydrin and the free base liberated by caustic soda; alternatively the amide may be reacted with chloracetic acid in water at 70-80 DEG C.; (6) N : N-dimethylethanolamine is esterified with coconut oil fatty acid and then quaternated with chloracetamide. Specifications 815,784 and 818,362, [Group III], are referred to.
GB20893/55A 1954-07-20 1955-07-19 Detergent preparations for the hair Expired GB818361A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH818361X 1954-07-20

Publications (1)

Publication Number Publication Date
GB818361A true GB818361A (en) 1959-08-12

Family

ID=4539166

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20893/55A Expired GB818361A (en) 1954-07-20 1955-07-19 Detergent preparations for the hair

Country Status (1)

Country Link
GB (1) GB818361A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3247119A (en) * 1962-02-06 1966-04-19 Armour & Co Cleansing composition and thickener therefor
US3322676A (en) * 1961-10-25 1967-05-30 Ciba Ltd Shampoos
GB2160421A (en) * 1984-06-08 1985-12-24 Dominion Chemicals Limited Hair and fabric conditioning preparation

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3322676A (en) * 1961-10-25 1967-05-30 Ciba Ltd Shampoos
US3247119A (en) * 1962-02-06 1966-04-19 Armour & Co Cleansing composition and thickener therefor
GB2160421A (en) * 1984-06-08 1985-12-24 Dominion Chemicals Limited Hair and fabric conditioning preparation

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