JPS62285995A - 亜硫酸化脂肪 - Google Patents
亜硫酸化脂肪Info
- Publication number
- JPS62285995A JPS62285995A JP62129571A JP12957187A JPS62285995A JP S62285995 A JPS62285995 A JP S62285995A JP 62129571 A JP62129571 A JP 62129571A JP 12957187 A JP12957187 A JP 12957187A JP S62285995 A JPS62285995 A JP S62285995A
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- fat
- sulfite
- alkali
- carbon atoms
- 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.)
- Pending
Links
- 239000003925 fat Substances 0.000 claims description 90
- 235000019197 fats Nutrition 0.000 claims description 90
- 239000000194 fatty acid Substances 0.000 claims description 70
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 69
- 229930195729 fatty acid Natural products 0.000 claims description 69
- -1 fatty acid ester Chemical class 0.000 claims description 56
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 52
- 239000000203 mixture Substances 0.000 claims description 42
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 150000004665 fatty acids Chemical group 0.000 claims description 34
- 229910052740 iodine Inorganic materials 0.000 claims description 27
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 26
- 239000011630 iodine Substances 0.000 claims description 26
- 239000003513 alkali Substances 0.000 claims description 21
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical compound C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 claims description 14
- 239000008041 oiling agent Substances 0.000 claims description 13
- 239000010698 whale oil Substances 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 125000003158 alcohol group Chemical group 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 235000019864 coconut oil Nutrition 0.000 claims description 9
- 239000003240 coconut oil Substances 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 9
- 235000019198 oils Nutrition 0.000 claims description 9
- 230000003647 oxidation Effects 0.000 claims description 9
- 238000007254 oxidation reaction Methods 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000010985 leather Substances 0.000 claims description 7
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 6
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 6
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 6
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005642 Oleic acid Substances 0.000 claims description 6
- 241000283222 Physeter catodon Species 0.000 claims description 6
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 6
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 claims description 5
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000004164 Wax ester Substances 0.000 claims description 5
- 239000003995 emulsifying agent Substances 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 5
- 239000003346 palm kernel oil Substances 0.000 claims description 5
- 235000019865 palm kernel oil Nutrition 0.000 claims description 5
- 239000003760 tallow Substances 0.000 claims description 5
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 claims description 5
- 229940117972 triolein Drugs 0.000 claims description 5
- 235000019386 wax ester Nutrition 0.000 claims description 5
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims description 4
- 235000021313 oleic acid Nutrition 0.000 claims description 4
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 150000003626 triacylglycerols Chemical class 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims 1
- 235000011130 ammonium sulphate Nutrition 0.000 claims 1
- ZETCGWYACBNPIH-UHFFFAOYSA-N azane;sulfurous acid Chemical compound N.OS(O)=O ZETCGWYACBNPIH-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims 1
- 230000026045 iodination Effects 0.000 description 15
- 238000006192 iodination reaction Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 150000004670 unsaturated fatty acids Chemical group 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 9
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 8
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 5
- 235000021323 fish oil Nutrition 0.000 description 5
- 150000004671 saturated fatty acids Chemical group 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 235000003441 saturated fatty acids Nutrition 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 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 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 241000737241 Cocos Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 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
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229940048937 re tann Drugs 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 235000021081 unsaturated fats Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B45/00—Formation or introduction of functional groups containing sulfur
- C07B45/02—Formation or introduction of functional groups containing sulfur of sulfo or sulfonyldioxy groups
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
- C14C9/02—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes using fatty or oily materials, e.g. fat liquoring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19863617691 DE3617691A1 (de) | 1986-05-26 | 1986-05-26 | Sulfitierte fettstoffe |
| DE3617691.5 | 1986-05-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS62285995A true JPS62285995A (ja) | 1987-12-11 |
Family
ID=6301669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62129571A Pending JPS62285995A (ja) | 1986-05-26 | 1987-05-26 | 亜硫酸化脂肪 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US4800045A (enEXAMPLES) |
| EP (1) | EP0247490B1 (enEXAMPLES) |
| JP (1) | JPS62285995A (enEXAMPLES) |
| BR (1) | BR8702670A (enEXAMPLES) |
| CA (1) | CA1297887C (enEXAMPLES) |
| DE (2) | DE3617691A1 (enEXAMPLES) |
| ES (1) | ES2018798B3 (enEXAMPLES) |
| IN (1) | IN168745B (enEXAMPLES) |
| MX (1) | MX168644B (enEXAMPLES) |
| TR (1) | TR22873A (enEXAMPLES) |
| ZA (1) | ZA873744B (enEXAMPLES) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102335099B1 (ko) * | 2021-04-22 | 2021-12-06 | 주식회사 엔게인 | 안정성이 높은 식물성 오일 유래 조영제 및 이의 제조방법 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3617691A1 (de) * | 1986-05-26 | 1987-12-03 | Henkel Kgaa | Sulfitierte fettstoffe |
| DE3826179C2 (de) * | 1988-08-02 | 1994-12-15 | Stockhausen Chem Fab Gmbh | Bei Raumtemperatur flüssige Derivate von natürlichen Fetten oder Ölen, Verfahren zu ihrer Herstellung und deren Verwendung |
| HRP930646A2 (en) * | 1992-04-10 | 1994-10-31 | Hoechst Ag | Leather greasing material |
| US5529704A (en) * | 1992-04-10 | 1996-06-25 | Hoechst Aktiengesellschaft | Leather fat-liquoring agents |
| DE4240159A1 (de) * | 1992-11-30 | 1994-06-01 | Henkel Kgaa | Sulfitierte Fettstoffe mit vermindertem Gehalt an freiem Hydrogensulfit |
| DE4405414A1 (de) * | 1994-02-21 | 1995-08-31 | Henkel Kgaa | Verwendung sulfierter Substanzen zur Fettung von Leder |
| DE4418942A1 (de) * | 1994-05-31 | 1995-12-07 | Henkel Kgaa | Mittel zur Fettung von Ledern und Pelzen |
| US5634948A (en) * | 1995-07-10 | 1997-06-03 | Boehme Filatex, Inc. | Low-fogging finish treatment for upholstery leather, and method |
| DE19917736A1 (de) * | 1999-04-20 | 2000-10-26 | Zschimmer & Schwarz Gmbh & Co | Mittel zur Ausrüstung von Leder |
| EP1299565B1 (de) * | 2000-06-16 | 2007-11-28 | Zschimmer & Schwarz GmbH & Co KG Chemische Fabriken | Mittel zur ausrüstung von leder |
| DE10242401A1 (de) * | 2002-09-12 | 2004-03-25 | Basf Ag | Fettungsmittel auf der Basis von Mischungen modifizierter, nativer Öle mit alkoxylierten Alkanolen, ihre Verwendung bei der Herstellung und/oder Behandlung von Leder und Häuten, sowie Verfahren zur Herstellung und/oder Behandlung von Leder und Häuten mit diesen Fettungsmitteln |
| EP1903889A4 (en) * | 2005-06-17 | 2009-12-23 | Nu Sci Lab | STABILIZATION OF OXIDIZED FATS |
| IT201900000585A1 (it) | 2019-01-14 | 2020-07-14 | Lamberti Spa | Metodo di perforazione di un pozzo sotterraneo |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2630408A (en) * | 1948-01-30 | 1953-03-03 | Nopco Chem Co | Fat composition |
| DE1016700B (de) * | 1954-05-15 | 1957-10-03 | Henkel & Cie Gmbh | Verfahren zur Herstellung von Umsetzungsprodukten ungesaettigter Fettsaeuren bzw. ihrer Ester oder Amide |
| US3522297A (en) * | 1966-01-14 | 1970-07-28 | Marathon Oil Co | Processes for the production of organic sulfonates |
| RO82311B1 (ro) * | 1983-03-26 | 1988-11-10 | Institutul De Cercetari Chimice | Produse de ungere pentru industria pielariei si procedeu de obtinere a acestora |
| EP0130753B1 (en) * | 1983-07-01 | 1987-12-09 | Lion Corporation | Process for producing sulfonate of unsaturated fatty acid ester |
| DE3437443A1 (de) * | 1984-10-12 | 1986-04-17 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von fettungsmittel fuer leder und pelze |
| DE3617691A1 (de) * | 1986-05-26 | 1987-12-03 | Henkel Kgaa | Sulfitierte fettstoffe |
-
1986
- 1986-05-26 DE DE19863617691 patent/DE3617691A1/de not_active Withdrawn
- 1986-12-24 IN IN1010/MAS/86A patent/IN168745B/en unknown
-
1987
- 1987-05-06 TR TR311/87A patent/TR22873A/xx unknown
- 1987-05-18 DE DE8787107190T patent/DE3766005D1/de not_active Expired - Fee Related
- 1987-05-18 ES ES87107190T patent/ES2018798B3/es not_active Expired - Lifetime
- 1987-05-18 EP EP87107190A patent/EP0247490B1/de not_active Expired - Lifetime
- 1987-05-20 MX MX006573A patent/MX168644B/es unknown
- 1987-05-25 CA CA000537840A patent/CA1297887C/en not_active Expired - Fee Related
- 1987-05-25 ZA ZA873744A patent/ZA873744B/xx unknown
- 1987-05-25 BR BR8702670A patent/BR8702670A/pt not_active IP Right Cessation
- 1987-05-26 JP JP62129571A patent/JPS62285995A/ja active Pending
- 1987-05-26 US US07/053,998 patent/US4800045A/en not_active Expired - Fee Related
-
1988
- 1988-10-11 US US07/255,909 patent/US4903362A/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102335099B1 (ko) * | 2021-04-22 | 2021-12-06 | 주식회사 엔게인 | 안정성이 높은 식물성 오일 유래 조영제 및 이의 제조방법 |
| US12201701B2 (en) | 2021-04-22 | 2025-01-21 | Engain Co., Ltd. | Vegetable oil-derived contrast agent with high stability and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| MX168644B (es) | 1993-06-02 |
| CA1297887C (en) | 1992-03-24 |
| US4800045A (en) | 1989-01-24 |
| DE3617691A1 (de) | 1987-12-03 |
| US4903362A (en) | 1990-02-27 |
| TR22873A (tr) | 1988-09-23 |
| IN168745B (enEXAMPLES) | 1991-06-01 |
| EP0247490A1 (de) | 1987-12-02 |
| ES2018798B3 (es) | 1991-05-16 |
| BR8702670A (pt) | 1988-02-23 |
| DE3766005D1 (de) | 1990-12-13 |
| EP0247490B1 (de) | 1990-11-07 |
| ZA873744B (en) | 1988-01-27 |
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