JPS61176553A - 脂肪酸の抽出方法 - Google Patents

脂肪酸の抽出方法

Info

Publication number: JPS61176553A
Authority: JP; Japan
Prior art keywords: lower fatty; fatty acid; fatty acids; acid; aqueous solution
Prior art date: 1985-01-30
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

JP1451085A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0219811B2 (fr

Inventor

Masaki Tanaka

雅紀田中

Naoki Kawada

河田　直紀

Takeshi Morinaga

森永　豪

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.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

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.)

1985-01-30

Filing date

1985-01-30

Publication date

1986-08-08

1985-01-30 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1985-01-30 Priority to JP1451085A priority Critical patent/JPS61176553A/ja

1986-08-08 Publication of JPS61176553A publication Critical patent/JPS61176553A/ja

1990-05-07 Publication of JPH0219811B2 publication Critical patent/JPH0219811B2/ja

Status Granted legal-status Critical Current

Links

235000014113 dietary fatty acids Nutrition 0.000 title claims abstract description 49
229930195729 fatty acid Natural products 0.000 title claims abstract description 49
239000000194 fatty acid Substances 0.000 title claims abstract description 49
150000004665 fatty acids Chemical class 0.000 title claims abstract description 49
238000000034 method Methods 0.000 title claims abstract description 13
239000007864 aqueous solution Substances 0.000 claims abstract description 16
150000003512 tertiary amines Chemical class 0.000 claims abstract description 14
238000009835 boiling Methods 0.000 claims abstract description 12
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims abstract description 12
239000012046 mixed solvent Substances 0.000 claims abstract description 10
150000003138 primary alcohols Chemical class 0.000 claims abstract description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 4
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims 2
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 39
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract description 12
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract description 12
238000000605 extraction Methods 0.000 abstract description 11
239000008346 aqueous phase Substances 0.000 abstract description 9
XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 abstract description 9
238000005192 partition Methods 0.000 abstract description 9
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract description 6
238000000855 fermentation Methods 0.000 abstract description 6
230000004151 fermentation Effects 0.000 abstract description 6
235000019253 formic acid Nutrition 0.000 abstract description 6
235000019260 propionic acid Nutrition 0.000 abstract description 6
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 abstract description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
230000000694 effects Effects 0.000 abstract description 4
239000000839 emulsion Substances 0.000 abstract description 3
238000000746 purification Methods 0.000 abstract description 3
238000000926 separation method Methods 0.000 abstract description 3
235000011054 acetic acid Nutrition 0.000 abstract description 2
238000010276 construction Methods 0.000 abstract description 2
-1 n-hexanol Chemical class 0.000 abstract 2
150000001875 compounds Chemical class 0.000 abstract 1
230000001747 exhibiting effect Effects 0.000 abstract 1
239000002904 solvent Substances 0.000 description 9
239000003085 diluting agent Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000004821 distillation Methods 0.000 description 3
150000001412 amines Chemical class 0.000 description 2
238000010586 diagram Methods 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
VBCJJAZGEJSVTL-UHFFFAOYSA-N (Z)-18-methylnonadec-9-en-1-amine Chemical compound CC(CCCCCCCC=C/CCCCCCCCN)C VBCJJAZGEJSVTL-UHFFFAOYSA-N 0.000 description 1
HXQPUEQDBSPXTE-UHFFFAOYSA-N Diisobutylcarbinol Chemical compound CC(C)CC(O)CC(C)C HXQPUEQDBSPXTE-UHFFFAOYSA-N 0.000 description 1
235000009470 Theobroma cacao Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000061 acid fraction Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
244000240602 cacao Species 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
244000005700 microbiome Species 0.000 description 1
238000002156 mixing Methods 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
ZAYNEGYLQMBZHR-UHFFFAOYSA-N n-butyl-5,5,7,7-tetramethyl-n-(5,5,7,7-tetramethyloct-2-enyl)oct-2-en-1-amine Chemical compound CC(C)(C)CC(C)(C)CC=CCN(CCCC)CC=CCC(C)(C)CC(C)(C)C ZAYNEGYLQMBZHR-UHFFFAOYSA-N 0.000 description 1
239000012071 phase Substances 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000004904 shortening Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000003760 tallow Substances 0.000 description 1
ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP1451085A 1985-01-30 1985-01-30 脂肪酸の抽出方法 Granted JPS61176553A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1451085A JPS61176553A (ja)	1985-01-30	1985-01-30	脂肪酸の抽出方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1451085A JPS61176553A (ja)	1985-01-30	1985-01-30	脂肪酸の抽出方法

Publications (2)

Publication Number	Publication Date
JPS61176553A true JPS61176553A (ja)	1986-08-08
JPH0219811B2 JPH0219811B2 (fr)	1990-05-07

Family

ID=11863069

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1451085A Granted JPS61176553A (ja)	1985-01-30	1985-01-30	脂肪酸の抽出方法

Country Status (1)

Country	Link
JP (1)	JPS61176553A (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2007522136A (ja) *	2004-01-29	2007-08-09	ズィーケムインコーポレイテッド	有機酸の回収
JP2011517445A (ja) *	2008-03-20	2011-06-09	テートアンドライルテクノロジーリミテッド	第三級アミド溶媒からの酸の除去
WO2022239847A1 (fr)	2021-05-14	2022-11-17	リファインホールディングス株式会社	Procédé de collecte d'acide carboxylique
WO2024106470A1 (fr)	2022-11-16	2024-05-23	Ｓｐｉｂｅｒ株式会社	Procédé de production d'un corps façonné contenant une protéine et procédé de récupération d'acide carboxylique

1985
- 1985-01-30 JP JP1451085A patent/JPS61176553A/ja active Granted

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2007522136A (ja) *	2004-01-29	2007-08-09	ズィーケムインコーポレイテッド	有機酸の回収
JP2011517445A (ja) *	2008-03-20	2011-06-09	テートアンドライルテクノロジーリミテッド	第三級アミド溶媒からの酸の除去
WO2022239847A1 (fr)	2021-05-14	2022-11-17	リファインホールディングス株式会社	Procédé de collecte d'acide carboxylique
WO2024106470A1 (fr)	2022-11-16	2024-05-23	Ｓｐｉｂｅｒ株式会社	Procédé de production d'un corps façonné contenant une protéine et procédé de récupération d'acide carboxylique
EP4624642A1 (fr)	2022-11-16	2025-10-01	Spiber Inc.	Procédé de production d'un corps façonné contenant une protéine et procédé de récupération d'acide carboxylique

Also Published As

Publication number	Publication date
JPH0219811B2 (fr)	1990-05-07

Legal Events

Date	Code	Title	Description
2005-01-30	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
JPS6016410B2 (ja)	1985-04-25	カルボン酸をその水溶液から収得する方法
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JP2732904B2 (ja)	1998-03-30	シクロヘキサノールの分離法
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