GB841903A - Method of increasing the water vapour porosity of fat components and a composition therefore - Google Patents

Method of increasing the water vapour porosity of fat components and a composition therefore

Info

Publication number
GB841903A
GB841903A GB30810/57A GB3081057A GB841903A GB 841903 A GB841903 A GB 841903A GB 30810/57 A GB30810/57 A GB 30810/57A GB 3081057 A GB3081057 A GB 3081057A GB 841903 A GB841903 A GB 841903A
Authority
GB
United Kingdom
Prior art keywords
methyl
acid
ester
malonic
give
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
GB30810/57A
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.)
Wickhen Products Inc
Original Assignee
Wickhen Products Inc
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 Wickhen Products Inc filed Critical Wickhen Products Inc
Publication of GB841903A publication Critical patent/GB841903A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

In making compounds to increase the water vapour porosity of the fat component of cosmetic preparations (see Group VI) 2-methyl dodecanol is converted into its bromide by treatment with 48% HBr and reacted with sodium malonic ester to give 2-methyldodecyl malonic acid ester which is then saponified to give 2-methyl-dodecyl malonic acid which, on heating at 10 mm. pressure, decarboxylates to 4-methyl-myristic acid. This may be converted to the ethyl ester by boiling with an ethanol-toluene-mixture, the ester being reduced with lithium aluminium hydroxide to 4-methyl tetradecanol which is converted to the bromide which, with sodium malonic ester gives 4-methyl tetradecyl-1-malonic ester which, on saponification and decarboxylation gives-6-methyl palmitic acid from which, as above, 6-methyl hexadecanol may be produced and, as above, through the bromide and 6-methyl hexadecyl-1-malonic ester, and saponification and decarboxylation, give 8-methylstearic acid. This may be converted to its ethyl ester which is reduced to give 8-methyl octadecanol. Dihydro citronellol myristinate is prepared by reacting myristic acid chloride with dihydro citronellol in pyridine.ALSO:The water vapour porosity of the fat component of cosmetics is increased by adding thereto 1 to 10% by weight of a branched chain aliphatic compound having 5 to 20 carbon atoms in the open chain and having a branch chain containing less than 3 carbon atoms spaced at least 1 carbon atom from the end carbon atoms in the open chain and bring an alcohol or an acid or a straight chain ester of said alcohol or acid with said straight chain having 5 to 20 carbon atoms. The fat component may be the conventional fatty materials used in cosmetic creams, lotions and salves, such as lanolin, petrolatum, vegetable oils, waxes and fatty acids. Lists of acids alcohols, and esters are given and examples of the preparation of 4-methyl myristic acid, 6-methyl palmitic acid, 8-methyl stearic acid: 8-methyl octadecanol, 6-methyl hexadecanol: dihydro citroneleol myristate are given.
GB30810/57A 1956-10-18 1957-10-02 Method of increasing the water vapour porosity of fat components and a composition therefore Expired GB841903A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE841903X 1956-10-18

Publications (1)

Publication Number Publication Date
GB841903A true GB841903A (en) 1960-07-20

Family

ID=6768191

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30810/57A Expired GB841903A (en) 1956-10-18 1957-10-02 Method of increasing the water vapour porosity of fat components and a composition therefore

Country Status (1)

Country Link
GB (1) GB841903A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536810A (en) * 1965-07-23 1970-10-27 Clintwood Chem Co Cosmetic preparations containing isopropyl ester of methyl heptadecanoic acid

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536810A (en) * 1965-07-23 1970-10-27 Clintwood Chem Co Cosmetic preparations containing isopropyl ester of methyl heptadecanoic acid

Similar Documents

Publication Publication Date Title
US4278656A (en) Cosmetic composition containing kojic acid ester
US4098882A (en) Anti-solar composition
GB1405346A (en) Process for the conversion of sterols contained in vegetable and animal oils and fats into their fatty acid esters
Hopkins et al. Fatty acids of kenaf seed oil
KR840001518B1 (en) Process for the preparation of 3,7,11,15-tetramethyl-2,4,6,10,14-hexadeca pentaenoic acid
GB841903A (en) Method of increasing the water vapour porosity of fat components and a composition therefore
Wirth et al. The fatty acids of Trichophyton rubrum
US3729503A (en) Aromatic esters of terpene alcohols
JPS5427523A (en) Preparation of hydroxy fatty acid ester
JP2016113394A (en) Ascorbic acid derivative or its salt and cosmetic
JPS52806A (en) Preparation of ester
GB1229234A (en)
JPS607961B2 (en) fair skin cosmetics
Tulloch Absolute configurations of 13-hydroxydocosanoic and 17-hydroxyoctadecanoic acids
GB810377A (en) Fungicidal compositions
GB764432A (en) Improvements in or relating to herbicidal compositions
Potter et al. Factors involved in the spectrophotometric analysis of fats
GB760559A (en) Improvements in or relating to mouldable gel-like or solid compositions
GB1072659A (en) Pharmaceutical compositions comprising mono-glyceryl ether derivatives
Tiedt et al. 902. The components of wool wax. Part I. The aliphatic alcohols
GB999947A (en) Preparation of esters
GB669205A (en) Process for the manufacture of esters of cholesterol and of cosmetic preparations including such esters
GB1013946A (en) Antioxidant comprising aliphatic esters
Toyama et al. Thermal Decomposition of Some Acetoxyoctadecenoates and Acetoxyoctadecadienoates
GB751753A (en) Improvements in or relating to the manufacture of primary alcohols of the vitamin a-series