JPS61186347A - 新規ソルビト−ルオレイン酸エステル - Google Patents
新規ソルビト−ルオレイン酸エステルInfo
- Publication number
- JPS61186347A JPS61186347A JP60026831A JP2683185A JPS61186347A JP S61186347 A JPS61186347 A JP S61186347A JP 60026831 A JP60026831 A JP 60026831A JP 2683185 A JP2683185 A JP 2683185A JP S61186347 A JPS61186347 A JP S61186347A
- Authority
- JP
- Japan
- Prior art keywords
- oleic acid
- sorbitol
- reaction
- formula
- acid ester
- 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.)
- Granted
Links
- -1 sorbitol oleic acid ester Chemical class 0.000 title claims abstract description 9
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 13
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims abstract description 11
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims abstract description 11
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000005642 Oleic acid Substances 0.000 claims abstract description 11
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims abstract description 11
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000002252 acyl group Chemical group 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract description 11
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract description 11
- 239000000600 sorbitol Substances 0.000 abstract description 11
- 102000004882 Lipase Human genes 0.000 abstract description 7
- 108090001060 Lipase Proteins 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 239000004367 Lipase Substances 0.000 abstract description 6
- 235000019421 lipase Nutrition 0.000 abstract description 6
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 239000002537 cosmetic Substances 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- 239000002736 nonionic surfactant Substances 0.000 abstract description 3
- 231100000252 nontoxic Toxicity 0.000 abstract description 3
- 230000003000 nontoxic effect Effects 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract description 3
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 2
- 230000000259 anti-tumor effect Effects 0.000 abstract description 2
- 235000013305 food Nutrition 0.000 abstract description 2
- 230000008635 plant growth Effects 0.000 abstract description 2
- 102000004157 Hydrolases Human genes 0.000 abstract 1
- 108090000604 Hydrolases Proteins 0.000 abstract 1
- 239000012295 chemical reaction liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 9
- 150000005690 diesters Chemical class 0.000 description 9
- 229940088598 enzyme Drugs 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 229940049964 oleate Drugs 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 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 2
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WERKSKAQRVDLDW-ANOHMWSOSA-N [(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO WERKSKAQRVDLDW-ANOHMWSOSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 150000003333 secondary alcohols Chemical class 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- 241000159512 Geotrichum Species 0.000 description 1
- 241000108056 Monas Species 0.000 description 1
- 241000235395 Mucor Species 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000002026 chloroform extract Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000003308 immunostimulating effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 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
- A61K8/37—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
- 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)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60026831A JPS61186347A (ja) | 1985-02-14 | 1985-02-14 | 新規ソルビト−ルオレイン酸エステル |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60026831A JPS61186347A (ja) | 1985-02-14 | 1985-02-14 | 新規ソルビト−ルオレイン酸エステル |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61186347A true JPS61186347A (ja) | 1986-08-20 |
| JPS6256142B2 JPS6256142B2 (enrdf_load_stackoverflow) | 1987-11-24 |
Family
ID=12204211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60026831A Granted JPS61186347A (ja) | 1985-02-14 | 1985-02-14 | 新規ソルビト−ルオレイン酸エステル |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61186347A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2646439A1 (fr) * | 1989-04-28 | 1990-11-02 | Gattefosse Ets Sa | Procede pour la preparation de sucroesters par reaction d'un sucre et d'un acide gras en milieu solvant et en presence d'une enzyme, et sucroesters ainsi prepares |
| WO2000027195A1 (fr) * | 1998-03-13 | 2000-05-18 | Meiji Milk Products Co., Ltd. | Agent insecticide, acaricide et antibacterien pour plante |
| JP2011207987A (ja) * | 2010-03-29 | 2011-10-20 | Sumitomo Chemical Co Ltd | 樹脂用の加工安定化剤、該加工安定化剤を含む樹脂組成物、および樹脂の加工安定性を向上させる方法 |
-
1985
- 1985-02-14 JP JP60026831A patent/JPS61186347A/ja active Granted
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2646439A1 (fr) * | 1989-04-28 | 1990-11-02 | Gattefosse Ets Sa | Procede pour la preparation de sucroesters par reaction d'un sucre et d'un acide gras en milieu solvant et en presence d'une enzyme, et sucroesters ainsi prepares |
| WO2000027195A1 (fr) * | 1998-03-13 | 2000-05-18 | Meiji Milk Products Co., Ltd. | Agent insecticide, acaricide et antibacterien pour plante |
| JP2011207987A (ja) * | 2010-03-29 | 2011-10-20 | Sumitomo Chemical Co Ltd | 樹脂用の加工安定化剤、該加工安定化剤を含む樹脂組成物、および樹脂の加工安定性を向上させる方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6256142B2 (enrdf_load_stackoverflow) | 1987-11-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0223960B1 (en) | Process for the production of arachidonic acid-containing lipids | |
| US4665029A (en) | Heat-resistant lipase | |
| US3634195A (en) | Production of lipase | |
| IE63272B1 (en) | The glycosidase inhibitor salbostatin, process fo r its preparation and its use | |
| US3677902A (en) | Preparation of amyloglucosidase | |
| Valero et al. | Lipase production by Candida rugosa: fermentation behaviour | |
| IL24529A (en) | Process for preparing cephalosporin derivatives | |
| EP0688871A2 (en) | Preparation of phytosphingosine derivative | |
| JPH0734752B2 (ja) | アラキドン酸及びこれを含有する脂質の製造方法 | |
| US5089521A (en) | 10-membered ring lactones, a process for the preparation thereof, and the use thereof | |
| JPS61186347A (ja) | 新規ソルビト−ルオレイン酸エステル | |
| US5315038A (en) | Microorganism for breaking down moenomycins, a process for the breakdown, and the use of the breakdown products | |
| US5011952A (en) | Phospholipase A2 inhibitor | |
| JPH0246294A (ja) | ストレプトミセス属微生物からのアングサイクリノンおよびその製造方法 | |
| EP0290136A2 (en) | 7-Beta-substituted-3-lower alkanoylacetoxymethyl-7-alpha-methoxy-3-cephem-4-carboxylic acid and process for production of same | |
| US5229281A (en) | Process for production of optically active 3-methyladipic acid from squalene using candida lipolytica | |
| JPH0494693A (ja) | アフィジコリンの製造法 | |
| KR100260837B1 (ko) | 광학활성 카본산 및 그 거울상 이성체 에스테르의 제조방법 | |
| JPS6094091A (ja) | 光学活性カルボン酸エステルの製造法 | |
| SU1472502A1 (ru) | Способ получени бактериальной холинэстеразы | |
| US5217887A (en) | Process for production of (r) methylsuccinic acid from squalene using candida lipolytica | |
| US3928134A (en) | Microbiological reduction of 7-(2(3-hydroxy-1-octenyl)-5-oxo-3-cyclopentel-1-yl)-5-heptenoic acid and related compounds | |
| EP0188628A1 (en) | Process for producing fatty acids by fermentation | |
| KR790001711B1 (ko) | 생리활성물질 a f 2562의 제조법 | |
| JPS6012993A (ja) | 光学活性カルボン酸の製造法 |