DK0805210T3 - Fremgangsmåde til isolering af 2-keto-L-gulonsyre - Google Patents

Fremgangsmåde til isolering af 2-keto-L-gulonsyre

Info

Publication number: DK0805210T3
Authority: DK; Denmark
Prior art keywords: acid; keto; stage; gulonic; low
Prior art date: 1996-04-30

Application number

DK97106678T

Other languages

Danish (da)

English (en)

Inventor

Ralf Duempelmann

Tomislav Keglevic

Original Assignee

Hoffmann La Roche

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.)

1996-04-30

Filing date

1997-04-23

Publication date

2003-07-14

1997-04-23 Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche

2003-07-14 Application granted granted Critical

2003-07-14 Publication of DK0805210T3 publication Critical patent/DK0805210T3/da

Links

VBUYCZFBVCCYFD-NUNKFHFFSA-N 2-dehydro-L-idonic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)C(=O)C(O)=O VBUYCZFBVCCYFD-NUNKFHFFSA-N 0.000 title abstract 6
VBUYCZFBVCCYFD-UHFFFAOYSA-N D-arabino-2-Hexulosonic acid Natural products OCC(O)C(O)C(O)C(=O)C(O)=O VBUYCZFBVCCYFD-UHFFFAOYSA-N 0.000 title abstract 6
238000000034 method Methods 0.000 title abstract 2
239000002253 acid Substances 0.000 abstract 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 3
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 abstract 3
230000001476 alcoholic effect Effects 0.000 abstract 3
229910052708 sodium Inorganic materials 0.000 abstract 3
239000011734 sodium Substances 0.000 abstract 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
125000005907 alkyl ester group Chemical group 0.000 abstract 2
238000002425 crystallisation Methods 0.000 abstract 2
150000003839 salts Chemical class 0.000 abstract 2
235000011149 sulphuric acid Nutrition 0.000 abstract 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
230000003197 catalytic effect Effects 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 abstract 1
238000001816 cooling Methods 0.000 abstract 1
239000013078 crystal Substances 0.000 abstract 1
239000002178 crystalline material Substances 0.000 abstract 1
238000006073 displacement reaction Methods 0.000 abstract 1
238000001704 evaporation Methods 0.000 abstract 1
230000008020 evaporation Effects 0.000 abstract 1
238000000855 fermentation Methods 0.000 abstract 1
230000004151 fermentation Effects 0.000 abstract 1
238000001914 filtration Methods 0.000 abstract 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
150000002500 ions Chemical class 0.000 abstract 1
239000000463 material Substances 0.000 abstract 1
238000003801 milling Methods 0.000 abstract 1
229910017604 nitric acid Inorganic materials 0.000 abstract 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 1
238000004064 recycling Methods 0.000 abstract 1
159000000000 sodium salts Chemical class 0.000 abstract 1
239000001117 sulphuric acid Substances 0.000 abstract 1
238000001238 wet grinding Methods 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/58—Aldonic, ketoaldonic or saccharic acids
- C12P7/60—2-Ketogulonic acid

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Zoology (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Microbiology (AREA)
General Chemical & Material Sciences (AREA)
Biotechnology (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

DK97106678T 1996-04-30 1997-04-23 Fremgangsmåde til isolering af 2-keto-L-gulonsyre DK0805210T3 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP96106829		1996-04-30
EP97102766		1997-02-20

Publications (1)

Publication Number	Publication Date
DK0805210T3 true DK0805210T3 (da)	2003-07-14

Family

ID=26141900

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK97106678T DK0805210T3 (da)	1996-04-30	1997-04-23	Fremgangsmåde til isolering af 2-keto-L-gulonsyre

Country Status (10)

Country	Link
US (1)	US5852211A (fr)
EP (1)	EP0805210B1 (fr)
JP (1)	JP3976832B2 (fr)
CN (1)	CN1155554C (fr)
AT (1)	ATE234931T1 (fr)
BR (1)	BR9701962A (fr)
DE (1)	DE59709535D1 (fr)
DK (1)	DK0805210T3 (fr)
ES (1)	ES2192630T3 (fr)
ID (1)	ID16816A (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6153791A (en) *	1999-08-02	2000-11-28	Archer-Daniels-Midland Company	Process for purifying 2-keto-L-gulonic acid
CN1372537A (zh) *	1999-08-03	2002-10-02	阿彻-丹尼尔斯-米德兰公司	回收有机酸的方法
US6902917B1 (en)	1999-08-03	2005-06-07	Archer-Daniels-Midland Company	Process for recovery of organic acids from fermentration broths
US6670505B1 (en)	2000-03-07	2003-12-30	Eastman Chemical Company	Process for the recovery of organic acids from aqueous solutions
US7137711B1 (en)	2000-03-21	2006-11-21	Leonard Reiffel	Multi-user retro reflector data input
KR100786898B1 (ko)	2000-05-03	2007-12-17	레오나드 레이필	듀얼 모드 데이터 이미징 제품
US6320061B1 (en)	2000-06-05	2001-11-20	Eastman Chemical Company	Solvent exchange process
US7034803B1 (en)	2000-08-18	2006-04-25	Leonard Reiffel	Cursor display privacy product
ATE400840T1 (de) *	2000-08-18	2008-07-15	Leonard Reiffel	Anmerkungs-abbildungs-datenprodukt
AU2002228950A1 (en) *	2000-12-15	2002-06-24	Leonard Reiffel	Imaged coded data source tracking product
EP1354471A4 (fr) *	2000-12-15	2006-02-08	Leonard Reiffel	Produit d'entree de donnees d'une source de donnees codees multi-usage multi-source multi-imageur
WO2002048947A1 (fr) *	2000-12-15	2002-06-20	Leonard Reiffel	Produit transducteur source de donnees codees imagees
WO2002086807A1 (fr) *	2001-04-19	2002-10-31	Leonard Reiffel	Acquisition de donnees d'une source de donnees codees, par imagerie combinee
GB0119864D0 (en)	2001-08-15	2001-10-10	Cerestar Holding Bv	Process for the manufacture of 2-keto-L-gulonic acid
DE10149869A1 (de) *	2001-10-10	2003-04-24	Basf Ag	Verfahren zur Isolierung von Salzen von organischen Säuren aus einer Fermentationsbrühe und zur Freisetzung der organischen Säure
US20060291797A1 (en) *	2003-05-27	2006-12-28	Leonard Reiffel	Multi-imager multi-source multi-use coded data source data input product
CN100353158C (zh) *	2004-08-24	2007-12-05	天津理工大学	一种2－酮基－l－古龙酸含量的分析方法
CN102242178A (zh) *	2011-06-21	2011-11-16	安徽丰原发酵技术工程研究有限公司	一种2-酮基-l-古龙酸的制备方法
JP2015508758A (ja) *	2012-02-08	2015-03-23	ピュラックバイオケムビー．ブイ．	カルボキシレートの酸性化
CN111943836A (zh) *	2019-05-16	2020-11-17	帝斯曼知识产权资产管理有限公司	回收2-酮-l-古洛糖酸的改进方法
CN119528719B (zh) *	2024-11-07	2025-10-24	浙江工业大学	一种盐析萃取耦合结晶分离纯化发酵液中古龙酸的方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3381027A (en) *	1964-04-22	1968-04-30	Hoffmann La Roche	Preparation and recovery of methyl 2-ketogluconate
JPS5266684A (en) *	1975-12-01	1977-06-02	Shionogi & Co Ltd	Purification and separation of 2-keto-l-glonic acid
JPS58177986A (ja) *	1982-04-09	1983-10-18	Shionogi & Co Ltd	Ｌ−アスコルビン酸の製造方法
DE3831070A1 (de) *	1988-09-13	1990-03-22	Basf Ag	Verfahren zur isolierung von 2-keto-polyhdroxy-c(pfeil abwaerts)6(pfeil abwaerts)-carbonsaeuren, insbesondere von 2-keto-l-gulonsaeure aus waessrigen fermentationsaustraegen
FR2636343B1 (fr) *	1988-09-13	1994-11-25	Rhone Poulenc Sante
FR2648136B1 (fr) *	1989-06-12	1994-06-17	Rhone Poulenc Sante	Procede de preparation de l'acide ascorbique
CH678057A5 (de) *	1989-06-26	1991-07-31	Enco Eng Ag	Verfahren zur herstellung von natrium- oder kalium-l-ascorbat.
CN1122802A (zh) *	1994-12-28	1996-05-22	华东理工大学	古龙酸钠定量地转化制取抗坏血酸的方法

1997
- 1997-04-15 JP JP09680997A patent/JP3976832B2/ja not_active Expired - Lifetime
- 1997-04-17 US US08/842,923 patent/US5852211A/en not_active Expired - Fee Related
- 1997-04-22 ID IDP971340A patent/ID16816A/id unknown
- 1997-04-23 ES ES97106678T patent/ES2192630T3/es not_active Expired - Lifetime
- 1997-04-23 AT AT97106678T patent/ATE234931T1/de not_active IP Right Cessation
- 1997-04-23 EP EP97106678A patent/EP0805210B1/fr not_active Expired - Lifetime
- 1997-04-23 DK DK97106678T patent/DK0805210T3/da active
- 1997-04-23 DE DE59709535T patent/DE59709535D1/de not_active Expired - Fee Related
- 1997-04-29 CN CNB971109893A patent/CN1155554C/zh not_active Expired - Fee Related
- 1997-04-30 BR BR9701962A patent/BR9701962A/pt active Search and Examination

Also Published As

Publication number	Publication date
EP0805210A3 (fr)	1999-07-14
BR9701962A (pt)	1998-09-15
CN1169978A (zh)	1998-01-14
EP0805210A2 (fr)	1997-11-05
JP3976832B2 (ja)	2007-09-19
CN1155554C (zh)	2004-06-30
EP0805210B1 (fr)	2003-03-19
DE59709535D1 (de)	2003-04-24
ES2192630T3 (es)	2003-10-16
US5852211A (en)	1998-12-22
JPH1053556A (ja)	1998-02-24
ATE234931T1 (de)	2003-04-15
ID16816A (id)	1997-11-13

Publication	Publication Date	Title
DK0805210T3 (da)	2003-07-14	Fremgangsmåde til isolering af 2-keto-L-gulonsyre
DK152488B (da)	1988-03-07	Fremgangsmaade til separering af (+)-6-methoxy-alfa-methyl-2-naphthaleneddikesyre eller salte deraf fra en blanding af (+)- og (-)-6-methoxy-alfa-methyl-2-naphthaleneddikesyre eller salte deraf
JPS57134498A (en)	1982-08-19	Anhydrous crystalline maltitol and its preparation and use
KR940009194A (ko)	1994-05-20	클라불란산 칼륨염의 제조 방법
US4395571A (en)	1983-07-26	Process for the preparation of d,1-2-(6-methoxy-2-naphthyl)propionic acid
EP1310504A4 (fr)	2004-02-25	Procede de production de tagatose cristallin
EE9800361A (et)	1999-08-16	Meetod bensüülalkoholi valmistamiseks
CN1028169C (zh)	1995-04-12	直接分离巯甲丙脯酸的方法
CA2026374A1 (fr)	1991-04-12	Recuperation de sel d'ida et de glauber de liqueurs residuaires de cristallisation
EP0065867B1 (fr)	1985-09-11	Résolution optique de DL-cystéine
US5229087A (en)	1993-07-20	Process for the preparation of titanium dioxide
US2921959A (en)	1960-01-19	Process of resolving dl-serine
JPS6174588A (ja)	1986-04-16	乳酸エステルの製法
Fargher et al.	1921	LXXVIII.—4-β-Methylaminoethylglyoxaline
ATE201026T1 (de)	2001-05-15	Verfahren zur herstellung von salzen von erythromicyn, roxithromicyn, clarythromicyn und azithromycin
JPS6422849A (en)	1989-01-25	Purification of 3-(3,4-dihydroxyphenyl)serine
CN1062560C (zh)	2001-02-28	双氧噁噻嗪盐类化合物的分离和精制方法
DK157003B (da)	1989-10-30	Anvendelse af n-methyl-d-glucamin eller salte deraf som spaltningsmiddel ved fremstillingen af (+)-6-methoxy-alfa-methyl-2-naphthaleneddikesyre
Haworth et al.	1940	200. The constituents of natural phenolic resins. Part XVII. A synthesis of l-matairesinol
US5334746A (en)	1994-08-02	Process for producing α-L-aspartyl-L-phenylalanine methyl ester
KR940014789A (ko)	1994-07-19	엘(l)-페닐알라닌의 회수방법
KR940000422A (ko)	1994-01-03	L-페닐알라닌 메틸 에스테르의 제조방법
JPH06306029A (ja)	1994-11-01	新規フェニルアラニン塩結晶とその製造法
IL37976A (en)	1974-06-30	Crystalline hydrate of trisodium d-fructose-1,6-diphosphoric acid and process for the preparation thereof
JPH0523248B2 (fr)	1993-04-02