DE4023600A1 - Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden - Google Patents

Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden

Info

Publication number: DE4023600A1
Authority: DE; Germany
Prior art keywords: weight; carbon atoms; dispersions; fatty acid; acid
Prior art date: 1990-07-25
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE4023600A

Other languages

German (de)

English (en)

Inventor

Thomas Dr Foerster

Holger Dr Tesmannn

Soraya Shamsai

Michael Schaaf

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.)

Henkel AG and Co KGaA

Original Assignee

Henkel AG and Co KGaA

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.)

1990-07-25

Filing date

1990-07-25

Publication date

1992-01-30

1990-07-25 Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA

1990-07-25 Priority to DE4023600A priority Critical patent/DE4023600A1/de

1991-07-17 Priority to PCT/EP1991/001335 priority patent/WO1992001507A2/fr

1991-07-17 Priority to JP3512178A priority patent/JPH05509087A/ja

1992-01-30 Publication of DE4023600A1 publication Critical patent/DE4023600A1/de

Status Withdrawn legal-status Critical Current

Links

239000006185 dispersion Substances 0.000 title claims abstract description 30
239000000194 fatty acid Substances 0.000 title claims abstract description 23
235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 21
229930195729 fatty acid Natural products 0.000 title claims abstract description 21
150000004665 fatty acids Chemical class 0.000 title claims description 19
230000009969 flowable effect Effects 0.000 title description 4
239000003921 oil Substances 0.000 claims abstract description 18
239000002253 acid Substances 0.000 claims abstract description 11
150000003839 salts Chemical class 0.000 claims abstract description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052783 alkali metal Inorganic materials 0.000 claims abstract 2
150000001340 alkali metals Chemical class 0.000 claims abstract 2
125000004432 carbon atom Chemical group C* 0.000 claims description 21
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 13
125000005456 glyceride group Chemical group 0.000 claims description 13
-1 alkaline earth metal salts Chemical class 0.000 claims description 12
239000002270 dispersing agent Substances 0.000 claims description 10
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 8
239000003792 electrolyte Substances 0.000 claims description 7
150000002191 fatty alcohols Chemical class 0.000 claims description 5
229920006395 saturated elastomer Polymers 0.000 claims description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
150000005690 diesters Chemical class 0.000 claims description 4
239000000839 emulsion Substances 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
239000005662 Paraffin oil Substances 0.000 claims description 3
229920000151 polyglycol Polymers 0.000 claims description 3
239000010695 polyglycol Substances 0.000 claims description 3
150000004671 saturated fatty acids Chemical class 0.000 claims description 3
235000003441 saturated fatty acids Nutrition 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
LPLLVINFLBSFRP-UHFFFAOYSA-N 2-methylamino-1-phenylpropan-1-one Chemical compound CNC(C)C(=O)C1=CC=CC=C1 LPLLVINFLBSFRP-UHFFFAOYSA-N 0.000 claims 1
240000003023 Cosmos bipinnatus Species 0.000 claims 1
235000005956 Cosmos caudatus Nutrition 0.000 claims 1
229910052500 inorganic mineral Inorganic materials 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
239000011707 mineral Substances 0.000 claims 1
239000003995 emulsifying agent Substances 0.000 abstract description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
235000019198 oils Nutrition 0.000 description 14
239000000203 mixture Substances 0.000 description 7
239000000047 product Substances 0.000 description 7
150000002148 esters Chemical class 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000003513 alkali Substances 0.000 description 5
235000011187 glycerol Nutrition 0.000 description 5
150000007513 acids Chemical class 0.000 description 4
150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 4
239000000499 gel Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
150000003626 triacylglycerols Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
239000003925 fat Substances 0.000 description 3
235000019197 fats Nutrition 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
235000013305 food Nutrition 0.000 description 2
150000002314 glycerols Chemical class 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
150000002632 lipids Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
239000001993 wax Substances 0.000 description 2
WFXHUBZUIFLWCV-UHFFFAOYSA-N (2,2-dimethyl-3-octanoyloxypropyl) octanoate Chemical compound CCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCC WFXHUBZUIFLWCV-UHFFFAOYSA-N 0.000 description 1
CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
GKAVJEXMEIQCEW-UHFFFAOYSA-N 1,3-bis(6-methylheptyl)cyclohexane Chemical compound CC(C)CCCCCC1CCCC(CCCCCC(C)C)C1 GKAVJEXMEIQCEW-UHFFFAOYSA-N 0.000 description 1
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
UKIARGZKGOGJNE-UHFFFAOYSA-N 1-(16-methylheptadecanoyloxy)butyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(CCC)OC(=O)CCCCCCCCCCCCCCC(C)C UKIARGZKGOGJNE-UHFFFAOYSA-N 0.000 description 1
DHGISFWHDBPFBJ-UHFFFAOYSA-N 2-(11-methyldodecanoyloxy)ethyl 11-methyldodecanoate Chemical compound CC(C)CCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCC(C)C DHGISFWHDBPFBJ-UHFFFAOYSA-N 0.000 description 1
LWLRMRFJCCMNML-UHFFFAOYSA-N 2-ethylhexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CC)CCCC LWLRMRFJCCMNML-UHFFFAOYSA-N 0.000 description 1
SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
MWKPHOIHTLQZIY-UHFFFAOYSA-N 2-hexyldecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CCCCCC)CCCCCCCC MWKPHOIHTLQZIY-UHFFFAOYSA-N 0.000 description 1
RUDXBXPTJPNTSO-UHFFFAOYSA-N 2-octyldodecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC RUDXBXPTJPNTSO-UHFFFAOYSA-N 0.000 description 1
UIVPNOBLHXUKDX-UHFFFAOYSA-N 3,5,5-trimethylhexyl 3,5,5-trimethylhexanoate Chemical compound CC(C)(C)CC(C)CCOC(=O)CC(C)CC(C)(C)C UIVPNOBLHXUKDX-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
SJIDAAGFCNIAJP-UHFFFAOYSA-N 6-methylheptyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCC(C)C SJIDAAGFCNIAJP-UHFFFAOYSA-N 0.000 description 1
UBGYURICIGUKHC-UHFFFAOYSA-N 7-methyloctyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCC(C)C UBGYURICIGUKHC-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
TXZRBCSUYLEATA-GALHSAGASA-N [(z)-docos-13-enyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC TXZRBCSUYLEATA-GALHSAGASA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
JIQQDZLFBDITIG-UHFFFAOYSA-N bis(2-hexyldecyl) butanedioate Chemical compound CCCCCCCCC(CCCCCC)COC(=O)CCC(=O)OCC(CCCCCC)CCCCCCCC JIQQDZLFBDITIG-UHFFFAOYSA-N 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
ZYNDJIBBPLNPOW-UHFFFAOYSA-N eurucic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCCCCCC(=O)OC ZYNDJIBBPLNPOW-UHFFFAOYSA-N 0.000 description 1
125000001924 fatty-acyl group Chemical group 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000008103 glucose Substances 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
229940071870 hydroiodic acid Drugs 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229940100554 isononyl isononanoate Drugs 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
229940089456 isopropyl stearate Drugs 0.000 description 1
229940119170 jojoba wax Drugs 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000001630 malic acid Substances 0.000 description 1
235000011090 malic acid Nutrition 0.000 description 1
ZYNDJIBBPLNPOW-KHPPLWFESA-N methyl erucate Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(=O)OC ZYNDJIBBPLNPOW-KHPPLWFESA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
229940073769 methyl oleate Drugs 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000000199 molecular distillation Methods 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-N 0.000 description 1
ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
229940116351 sebacate Drugs 0.000 description 1
CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
229960005078 sorbitan sesquioleate Drugs 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1

Classifications

- 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
- 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
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
- 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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Birds (AREA)
Epidemiology (AREA)
Emergency Medicine (AREA)
Dermatology (AREA)
Colloid Chemistry (AREA)
Paper (AREA)
Cosmetics (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

DE4023600A 1990-07-25 1990-07-25 Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden Withdrawn DE4023600A1 (de)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
DE4023600A DE4023600A1 (de)	1990-07-25	1990-07-25	Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden
PCT/EP1991/001335 WO1992001507A2 (fr)	1990-07-25	1991-07-17	Dispersions coulantes et stables au stockage de glycerides partiels d'acide gras
JP3512178A JPH05509087A (ja)	1990-07-25	1991-07-17	脂肪酸部分グリセリドの貯蔵可能な流動性分散液

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE4023600A DE4023600A1 (de)	1990-07-25	1990-07-25	Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden

Publications (1)

Publication Number	Publication Date
DE4023600A1 true DE4023600A1 (de)	1992-01-30

Family

ID=6410975

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE4023600A Withdrawn DE4023600A1 (de)	1990-07-25	1990-07-25	Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden

Country Status (3)

Country	Link
JP (1)	JPH05509087A (fr)
DE (1)	DE4023600A1 (fr)
WO (1)	WO1992001507A2 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19703087A1 (de) *	1997-01-29	1998-07-30	Henkel Kgaa	Kosmetische PIT-Emulsionen
DE19724605A1 (de) *	1997-06-11	1998-12-17	Sueddeutsche Kalkstickstoff	Hydrophile, homogene Monogycerid-Formulierungen und Verfahren zu deren Herstellung

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2694494B1 (fr) *	1992-08-05	1994-09-30	Rhone Poulenc Chimie	Composition cosmétique contenant en suspension des particules non hydrosolubles.
FR2707162B1 (fr) *	1993-07-05	1995-09-29	Chanel	Formulation de base pour produit cosmétique, procédé de préparation et mascara.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2684948A (en) *	1950-12-12	1954-07-27	Atlas Powder Co	Stabilized wax emulsion
US3752770A (en) *	1970-05-13	1973-08-14	B Buddemeyer	Multifunctional emulsification agents
DE2511644C3 (de) *	1975-03-17	1978-09-21	Chemische Fabrik Gruenau Gmbh, 7918 Illertissen	Dispersionen von Gemischen aus Fettsäuremonoglyceriden und Fettsäurediglyceriden und deren Verwendung
DE3640755A1 (de) *	1986-11-28	1988-06-09	Henkel Kgaa	Fliessfaehiges perlglanzkonzentrat
JPH0745394B2 (ja) *	1987-01-28	1995-05-17	花王株式会社	保湿用皮膚化粧料
DE3819193A1 (de) *	1988-06-06	1989-12-07	Henkel Kgaa	Verfahren zur herstellung stabiler, niedrigviskoser oel-in-wasser-emulsionen polarer oelkomponenten

1990
- 1990-07-25 DE DE4023600A patent/DE4023600A1/de not_active Withdrawn
1991
- 1991-07-17 JP JP3512178A patent/JPH05509087A/ja active Pending
- 1991-07-17 WO PCT/EP1991/001335 patent/WO1992001507A2/fr not_active Ceased

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19703087A1 (de) *	1997-01-29	1998-07-30	Henkel Kgaa	Kosmetische PIT-Emulsionen
DE19703087C2 (de) *	1997-01-29	1999-04-22	Henkel Kgaa	Verwendung von PIT-Emulsionen
US6537562B1 (en)	1997-01-29	2003-03-25	Cognis Deutschland Gmbh & Co. Kg	Cosmetic PIT emulsions
DE19724605A1 (de) *	1997-06-11	1998-12-17	Sueddeutsche Kalkstickstoff	Hydrophile, homogene Monogycerid-Formulierungen und Verfahren zu deren Herstellung

Also Published As

Publication number	Publication date
WO1992001507A2 (fr)	1992-02-06
WO1992001507A3 (fr)	1992-03-05
JPH05509087A (ja)	1993-12-16

Publication	Publication Date	Title
EP0554292B1 (fr)	1994-12-21	Emulsions d'huile dans l'eau
EP0345586B1 (fr)	1992-07-01	Procédé de préparation d'une émulsion stable et peu visqueuse d'huile dans de l'eau avec des huiles polaires
EP0521981B1 (fr)	1994-12-28	Procede pour fabriquer des cremes aqueuses
DE4337030A1 (de)	1995-05-04	Verfahren zur Herstellung von Wachsdispersionen
EP0618840B1 (fr)	1995-08-30	Procede de preparation d'emulsions d'huile dans l'eau
EP0559013B1 (fr)	1995-08-09	Emulsion multiple liquide ou pâteuse, stable au stockage, du type H/E/H
EP0214568B1 (fr)	1990-04-25	Emulsion d'huile dans l'eau
EP0723432B1 (fr)	1998-12-30	Concentre d'emulsion coulant
DE4337041A1 (de)	1995-05-04	Verfahren zur Herstellung in Öl-in-Wasser-Emulsionen
DE4023600A1 (de)	1992-01-30	Fliessfaehige, lagerstabile dispersionen von fettsaeurepartialglyceriden
DE4338999C1 (de)	1994-10-13	Kaltwasseremulgierbare Mittel
WO1990007976A2 (fr)	1990-07-26	Dispersion de graisse non-ionique fluide
DE4128693A1 (de)	1993-03-04	Oel-in-wasser-emulsionen polarer oelkomponenten
DE2511644C3 (de)	1978-09-21	Dispersionen von Gemischen aus Fettsäuremonoglyceriden und Fettsäurediglyceriden und deren Verwendung
DE4104053A1 (de)	1992-08-13	Dispersionen von fettsaeurepartialglyceriden
DE19646878A1 (de)	1998-05-14	Verfahren zur Herstellung von ÖL-in-Wasser-Emulsionen
DE2623085C2 (de)	1987-01-08	Verwendung von Umsetzungsprodukten von Glycidylethern als Wasser-in-Öl-Emulgatoren
WO1992013511A1 (fr)	1992-08-20	Systemes stables a trois phases
DE1018180B (de)	1957-10-24	Verfahren zur Herstellung von Lithium-Calcium-Seifen-Schmierfetten

Legal Events

Date	Code	Title	Description
1995-07-13	8139	Disposal/non-payment of the annual fee