BE424182A - - Google Patents
Info
- Publication number
- BE424182A BE424182A BE424182DA BE424182A BE 424182 A BE424182 A BE 424182A BE 424182D A BE424182D A BE 424182DA BE 424182 A BE424182 A BE 424182A
- Authority
- BE
- Belgium
- Prior art keywords
- glycerin
- emi
- weight
- contain
- parts
- Prior art date
Links
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 32
- 235000011187 glycerol Nutrition 0.000 claims description 16
- 239000000344 soap Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- -1 aliphatic alcohols Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 239000003925 fat Substances 0.000 claims 2
- 239000011872 intimate mixture Substances 0.000 claims 2
- 150000002314 glycerols Chemical class 0.000 claims 1
- 239000000047 product Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 239000000314 lubricant Substances 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000012748 slip agent Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- DUXYWXYOBMKGIN-UHFFFAOYSA-N trimyristin Chemical compound CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCC DUXYWXYOBMKGIN-UHFFFAOYSA-N 0.000 description 2
- GBXRUYNQDDTQQS-UHFFFAOYSA-N 1-O-dodecylglycerol Chemical compound CCCCCCCCCCCCOCC(O)CO GBXRUYNQDDTQQS-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- BOBBGMZPCIFCRJ-GNNYBVKZSA-N OCC(O)CO.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O Chemical compound OCC(O)CO.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O BOBBGMZPCIFCRJ-GNNYBVKZSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 208000001431 Psychomotor Agitation Diseases 0.000 description 1
- 206010038743 Restlessness Diseases 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- GUTBHOXHMJMIQV-UHFFFAOYSA-N amino ethyl sulfate Chemical compound CCOS(=O)(=O)ON GUTBHOXHMJMIQV-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229940116364 hard fat Drugs 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE201626X | 1936-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE424182A true BE424182A (en]) |
Family
ID=5767188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE424182D BE424182A (en]) | 1936-11-17 |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE424182A (en]) |
| CH (1) | CH201626A (en]) |
| FR (1) | FR827095A (en]) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2532206A (en) * | 1946-07-01 | 1950-11-28 | Vodol Company | Ointment base of glycerine with phosphatide and petrolatum |
| US2514296A (en) * | 1947-12-19 | 1950-07-04 | Standard Oil Dev Co | Solvent resistant low temperature lubricant |
-
0
- BE BE424182D patent/BE424182A/fr unknown
-
1937
- 1937-09-24 FR FR827095D patent/FR827095A/fr not_active Expired
- 1937-10-25 CH CH201626D patent/CH201626A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR827095A (fr) | 1938-04-15 |
| CH201626A (de) | 1938-12-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1947989A (en) | Method of oxidizing hydrocarbons | |
| LU85789A1 (fr) | Utilisation dans les domaines therapeutique et cosmetique d'une solution anhydre de peroxyde d'hydrogene | |
| EP1743015A1 (fr) | Composition tensioactive, procede de preparation et cosmetique comprenant cette composition | |
| JPS6042318A (ja) | 化粧−薬学用油成分 | |
| FR2534923A1 (fr) | Ethers polyoxyalkyleniques du glycerol ou du 1,2-propanediol esterifies par un acide gras et/ou par l'acide isostearique, leur procede de fabrication ainsi que leur application comme epaississants ou solubilisants | |
| EP1412462B1 (fr) | Substitut de lanoline son procede d obtention et ses applications | |
| JPS5923320B2 (ja) | 分岐脂肪酸コレステリルエステル | |
| EP0028457A2 (en) | Cosmetic and emulsifier composition | |
| FR2549826A1 (fr) | Nouveaux ethers de polyols, leur procede de preparation et leur application en cosmetique | |
| BE424182A (en]) | ||
| CH458317A (fr) | Procédé de préparation de composés organiques de l'aluminium | |
| CH400118A (fr) | Procédé de préparation de sels de l'acide glycyrrhétinique et de sels de semi-esters de l'acide glycyrrhétinique | |
| CA1047505A (fr) | Production et applications de sulfoxydes organiques | |
| US957633A (en) | Ester from chaulmoogra-oil. | |
| US1996168A (en) | Process of producing solidified mineral oil preparation | |
| AT149988B (de) | Verfahren zur Darstellung von höhermolekularen Äthern. | |
| BE620530A (en]) | ||
| US1033841A (en) | Derivatives of metacresol with organic acids. | |
| FR2696467A1 (fr) | Procédé de préparation de monoesters d'acides gras du D-fructose et leur utilisation dans les domaines cosmétique, bucco-dentaire, pharmaceutique et alimentaire. | |
| DE151545C (en]) | ||
| DE270994C (en]) | ||
| BE655414A (en]) | ||
| DE215664C (en]) | ||
| BE488323A (en]) | ||
| CH285677A (fr) | Procédé de préparation de la 15-méthyl-cyclopentadécanol-2-one-1. |