JPS61139396A - リパ−ゼによるオキシステアリン酸の製造方法 - Google Patents

リパ−ゼによるオキシステアリン酸の製造方法

Info

Publication number: JPS61139396A
Authority: JP; Japan
Prior art keywords: castor oil; lipase; hydrogenated castor; reaction; hardened castor
Prior art date: 1984-12-11
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

Application number

JP59262450A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6253154B2 (2

Inventor

Hidekazu Nakagawa

英一中川

Koichi Murai

村井　孝一

Yuji Kawashima

川嶋　右次

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.)

New Japan Chemical Co Ltd

Original Assignee

New Japan Chemical Co Ltd

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.)

1984-12-11

Filing date

1984-12-11

Publication date

1986-06-26

1984-12-11 Application filed by New Japan Chemical Co Ltd filed Critical New Japan Chemical Co Ltd

1984-12-11 Priority to JP59262450A priority Critical patent/JPS61139396A/ja

1986-06-26 Publication of JPS61139396A publication Critical patent/JPS61139396A/ja

1987-11-09 Publication of JPS6253154B2 publication Critical patent/JPS6253154B2/ja

Status Granted legal-status Critical Current

Links

239000004367 Lipase Substances 0.000 title claims abstract description 20
102000004882 Lipase Human genes 0.000 title claims abstract description 20
108090001060 Lipase Proteins 0.000 title claims abstract description 20
235000019421 lipase Nutrition 0.000 title claims abstract description 20
238000004519 manufacturing process Methods 0.000 title claims description 7
ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 title abstract description 11
KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 title 1
239000004359 castor oil Substances 0.000 claims abstract description 21
235000019438 castor oil Nutrition 0.000 claims abstract description 21
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 claims abstract description 21
VLHZUYUOEGBBJB-UHFFFAOYSA-N hydroxy stearic acid Natural products OCCCCCCCCCCCCCCCCCC(O)=O VLHZUYUOEGBBJB-UHFFFAOYSA-N 0.000 claims abstract description 6
244000005700 microbiome Species 0.000 claims abstract description 5
230000003301 hydrolyzing effect Effects 0.000 claims abstract description 4
238000002844 melting Methods 0.000 abstract description 14
230000008018 melting Effects 0.000 abstract description 14
238000000034 method Methods 0.000 abstract description 14
239000003925 fat Substances 0.000 abstract description 12
238000006243 chemical reaction Methods 0.000 abstract description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
239000003921 oil Substances 0.000 abstract description 6
229940114072 12-hydroxystearic acid Drugs 0.000 abstract description 5
238000003756 stirring Methods 0.000 abstract description 5
241000588881 Chromobacterium Species 0.000 abstract description 2
241000235395 Mucor Species 0.000 abstract description 2
241000589516 Pseudomonas Species 0.000 abstract description 2
241000235527 Rhizopus Species 0.000 abstract description 2
238000006460 hydrolysis reaction Methods 0.000 description 11
238000000354 decomposition reaction Methods 0.000 description 9
230000007062 hydrolysis Effects 0.000 description 9
235000019197 fats Nutrition 0.000 description 8
238000007127 saponification reaction Methods 0.000 description 8
239000002253 acid Substances 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical group C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 4
239000008164 mustard oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
239000000243 solution Substances 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000010775 animal oil Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000011630 iodine Substances 0.000 description 3
239000000203 mixture Substances 0.000 description 3
235000015112 vegetable and seed oil Nutrition 0.000 description 3
239000008158 vegetable oil Substances 0.000 description 3
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
235000006200 Glycyrrhiza glabra Nutrition 0.000 description 2
241000909578 Nectandra Species 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
239000001110 calcium chloride Substances 0.000 description 2
229910001628 calcium chloride Inorganic materials 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
239000010446 mirabilite Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000758 substrate Substances 0.000 description 2
235000019871 vegetable fat Nutrition 0.000 description 2
238000004065 wastewater treatment Methods 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
DYBIGIADVHIODH-UHFFFAOYSA-N 2-nonylphenol;oxirane Chemical compound C1CO1.CCCCCCCCCC1=CC=CC=C1O DYBIGIADVHIODH-UHFFFAOYSA-N 0.000 description 1
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
241000223198 Humicola Species 0.000 description 1
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
230000032683 aging Effects 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000006664 bond formation reaction Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910001424 calcium ion Inorganic materials 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
235000020094 liqueur Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910001425 magnesium ion Inorganic materials 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
239000008213 purified water Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1

Landscapes

Preparation Of Compounds By Using Micro-Organisms (AREA)

JP59262450A 1984-12-11 1984-12-11 リパ−ゼによるオキシステアリン酸の製造方法 Granted JPS61139396A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP59262450A JPS61139396A (ja)	1984-12-11	1984-12-11	リパ−ゼによるオキシステアリン酸の製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59262450A JPS61139396A (ja)	1984-12-11	1984-12-11	リパ−ゼによるオキシステアリン酸の製造方法

Publications (2)

Publication Number	Publication Date
JPS61139396A true JPS61139396A (ja)	1986-06-26
JPS6253154B2 JPS6253154B2 (2)	1987-11-09

Family

ID=17375952

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59262450A Granted JPS61139396A (ja)	1984-12-11	1984-12-11	リパ−ゼによるオキシステアリン酸の製造方法

Country Status (1)

Country	Link
JP (1)	JPS61139396A (2)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2002036796A1 (de) *	2000-11-03	2002-05-10	Cognis Deutschland Gmbh & Co. Kg	Verfahren zur gewinnung von 12-hydroxystearinsäure
CN1112430C (zh) *	2000-08-24	2003-06-25	通辽市通华蓖麻化工有限责任公司	油脂化工产品12－羟基硬脂酸的制取方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN104946692B (zh) *	2015-06-10	2018-08-31	文水县国华油脂有限公司	氢化蓖麻油生物水解法制作12-羟基硬脂酸工艺

1984
- 1984-12-11 JP JP59262450A patent/JPS61139396A/ja active Granted

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN1112430C (zh) *	2000-08-24	2003-06-25	通辽市通华蓖麻化工有限责任公司	油脂化工产品12－羟基硬脂酸的制取方法
WO2002036796A1 (de) *	2000-11-03	2002-05-10	Cognis Deutschland Gmbh & Co. Kg	Verfahren zur gewinnung von 12-hydroxystearinsäure

Also Published As

Publication number	Publication date
JPS6253154B2 (2)	1987-11-09

Publication	Publication Date	Title
CN1066679A (zh)	1992-12-02	降低动植物油中含磷成分含量的方法
JP6409132B2 (ja)	2018-10-17	脂肪酸エステルの製造方法
CN113234698B (zh)	2023-06-09	一种氰基还原酶和加巴喷丁的制备方法
CN109957459B (zh)	2023-04-07	制备脂肪酸的方法及通过该方法获得的脂肪酸
US5968792A (en)	1999-10-19	Calcium activation of lipase enzyme in process of pressure splitting glycerides
JPS6253154B2 (2)	1987-11-09
US2463015A (en)	1949-03-01	Method of treating animal and vegetable oils
DE3854761D1 (de)	1996-01-18	Verfahren zur herstellung von hochreiner ölsäure durch hydrolyse von sonnenblumenkernöl.
US4123426A (en)	1978-10-31	Process for decomposing microbial cells
US4904586A (en)	1990-02-27	Enzymatic process for treating xanthan gums in order to improve the filterability of their aqueous solutions
JP2678915B2 (ja)	1997-11-19	脂肪酸の製造法
EP0906380A1 (en)	1999-04-07	Method for dewatering and purifying oil or fat
JPH0212465B2 (2)	1990-03-20
JP2718650B2 (ja)	1998-02-25	高度不飽和脂肪酸アルコールエステルの製造方法
KR910009932A (ko)	1991-06-28	(+)-호모 필로핀 산(hoopilopic acid) 및 그 염의 제조방법
US1967319A (en)	1934-07-24	Treatment of fats to produce fatty acids
CN116425612B (zh)	2024-11-22	一种废弃油脂生物柴油酯交换含醇粗甘油除碱脱油的方法
JPS60130396A (ja)	1985-07-11	長鎖不飽和脂肪酸含有油脂の加水分解方法
SU833750A1 (ru)	1981-05-30	Способ приготовлени белковогопЕНООбРАзОВАТЕл
CA2127628A1 (fr)	1995-01-10	Composition aqueuse d'acide sulfamique epaissie
JPH03504440A (ja)	1991-10-03	脂肪加水分解プロセス
US1972059A (en)	1934-08-28	Production of organic acids by the alkaline fusion of cellulosic materials
GB1053807A (2)	1900-01-01
KR940000778B1 (ko)	1994-01-31	효소의 지방분해에 의한 사료첨가제의 제조방법
CN1056255A (zh)	1991-11-20	蛋白泡沫灭火剂的制取方法

JPS61139396A - リパ−ゼによるオキシステアリン酸の製造方法 - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=17375952

Family Applications (1)

Country Status (1)

Cited By (2)

Families Citing this family (1)

Cited By (2)

Also Published As

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