NO328027B1 - Fremstilling av 4,4'-diketo beta-karotenderivater - Google Patents

Fremstilling av 4,4'-diketo beta-karotenderivater Download PDF

Info

Publication number: NO328027B1
Authority: NO; Norway
Prior art keywords: carotene; sodium; potassium; derivatives; bromate
Prior art date: 2001-09-13

Application number

NO20024266A

Other languages

English (en)

Norwegian (no)

Other versions

NO20024266L (no

NO20024266D0 (no

Inventor

George C Schloemer

Jeffrey L Davis

Danuta A Schloemer

Original Assignee

Dsm Ip Assets Bv

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.)

2001-09-13

Filing date

2002-09-06

Publication date

2009-11-10

2002-09-06 Application filed by Dsm Ip Assets Bv filed Critical Dsm Ip Assets Bv

2002-09-06 Publication of NO20024266D0 publication Critical patent/NO20024266D0/no

2003-03-14 Publication of NO20024266L publication Critical patent/NO20024266L/no

2009-11-10 Publication of NO328027B1 publication Critical patent/NO328027B1/no

Links

238000002360 preparation method Methods 0.000 title description 2
FDSDTBUPSURDBL-DKLMTRRASA-N canthaxanthin Chemical class CC=1C(=O)CCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)C(=O)CCC1(C)C FDSDTBUPSURDBL-DKLMTRRASA-N 0.000 title 1
239000000243 solution Substances 0.000 claims description 26
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 claims description 23
239000011734 sodium Substances 0.000 claims description 23
229910052708 sodium Inorganic materials 0.000 claims description 23
238000000034 method Methods 0.000 claims description 22
JKQXZKUSFCKOGQ-LQFQNGICSA-N Z-zeaxanthin Natural products C([C@H](O)CC=1C)C(C)(C)C=1C=CC(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC1=C(C)C[C@@H](O)CC1(C)C JKQXZKUSFCKOGQ-LQFQNGICSA-N 0.000 claims description 21
QOPRSMDTRDMBNK-RNUUUQFGSA-N Zeaxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCC(O)C1(C)C)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C QOPRSMDTRDMBNK-RNUUUQFGSA-N 0.000 claims description 21
JKQXZKUSFCKOGQ-LOFNIBRQSA-N all-trans-Zeaxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C JKQXZKUSFCKOGQ-LOFNIBRQSA-N 0.000 claims description 21
KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 claims description 21
235000010930 zeaxanthin Nutrition 0.000 claims description 21
239000001775 zeaxanthin Substances 0.000 claims description 21
229940043269 zeaxanthin Drugs 0.000 claims description 21
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical group ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 20
FDSDTBUPSURDBL-LOFNIBRQSA-N canthaxanthine Natural products CC=1C(=O)CCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)C(=O)CCC1(C)C FDSDTBUPSURDBL-LOFNIBRQSA-N 0.000 claims description 18
JEBFVOLFMLUKLF-IFPLVEIFSA-N Astaxanthin Natural products CC(=C/C=C/C(=C/C=C/C1=C(C)C(=O)C(O)CC1(C)C)/C)C=CC=C(/C)C=CC=C(/C)C=CC2=C(C)C(=O)C(O)CC2(C)C JEBFVOLFMLUKLF-IFPLVEIFSA-N 0.000 claims description 17
235000013793 astaxanthin Nutrition 0.000 claims description 17
MQZIGYBFDRPAKN-ZWAPEEGVSA-N astaxanthin Chemical compound C([C@H](O)C(=O)C=1C)C(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)C(=O)[C@@H](O)CC1(C)C MQZIGYBFDRPAKN-ZWAPEEGVSA-N 0.000 claims description 17
239000001168 astaxanthin Substances 0.000 claims description 17
229940022405 astaxanthin Drugs 0.000 claims description 17
239000007800 oxidant agent Substances 0.000 claims description 15
239000011648 beta-carotene Substances 0.000 claims description 14
229960002747 betacarotene Drugs 0.000 claims description 14
235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 14
OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 claims description 13
235000013734 beta-carotene Nutrition 0.000 claims description 13
TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 claims description 13
239000003960 organic solvent Substances 0.000 claims description 13
OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 claims description 13
OOUTWVMJGMVRQF-DOYZGLONSA-N Phoenicoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C(=O)C(O)CC1(C)C)C=CC=C(/C)C=CC2=C(C)C(=O)CCC2(C)C OOUTWVMJGMVRQF-DOYZGLONSA-N 0.000 claims description 11
239000007864 aqueous solution Substances 0.000 claims description 11
235000012682 canthaxanthin Nutrition 0.000 claims description 11
239000001659 canthaxanthin Substances 0.000 claims description 11
229940008033 canthaxanthin Drugs 0.000 claims description 11
XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 claims description 10
239000004153 Potassium bromate Substances 0.000 claims description 10
235000019396 potassium bromate Nutrition 0.000 claims description 10
229940094037 potassium bromate Drugs 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 claims description 8
235000010259 potassium hydrogen sulphite Nutrition 0.000 claims description 8
XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 claims description 7
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical class OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 6
150000001579 beta-carotenes Chemical class 0.000 claims description 6
238000002156 mixing Methods 0.000 claims description 6
235000010265 sodium sulphite Nutrition 0.000 claims description 5
125000000863 canthaxanthin group Chemical group 0.000 claims description 4
229940099427 potassium bisulfite Drugs 0.000 claims description 4
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 claims description 4
235000019252 potassium sulphite Nutrition 0.000 claims description 4
125000001695 zeaxanthin group Chemical group 0.000 claims description 4
239000003125 aqueous solvent Substances 0.000 claims description 3
229940079826 hydrogen sulfite Drugs 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
159000000001 potassium salts Chemical class 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 description 21
JKQXZKUSFCKOGQ-JLGXGRJMSA-N (3R,3'R)-beta,beta-carotene-3,3'-diol Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)C[C@@H](O)CC1(C)C JKQXZKUSFCKOGQ-JLGXGRJMSA-N 0.000 description 17
239000000203 mixture Substances 0.000 description 10
238000007254 oxidation reaction Methods 0.000 description 8
239000000047 product Substances 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 6
230000003647 oxidation Effects 0.000 description 6
239000004289 sodium hydrogen sulphite Substances 0.000 description 6
239000003153 chemical reaction reagent Substances 0.000 description 5
239000012071 phase Substances 0.000 description 5
230000002378 acidificating effect Effects 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000007787 solid Substances 0.000 description 4
241000251468 Actinopterygii Species 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
235000021466 carotenoid Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000010410 layer Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000012044 organic layer Substances 0.000 description 3
230000001590 oxidative effect Effects 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241000195493 Cryptophyta Species 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
125000000746 allylic group Chemical group 0.000 description 2
239000003674 animal food additive Substances 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical class OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 2
-1 carotenoid compounds Chemical class 0.000 description 2
150000001747 carotenoids Chemical class 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000000855 fermentation Methods 0.000 description 2
230000004151 fermentation Effects 0.000 description 2
235000019688 fish Nutrition 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000000049 pigment Substances 0.000 description 2
244000144977 poultry Species 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
235000015424 sodium Nutrition 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
238000006257 total synthesis reaction Methods 0.000 description 2
OOUTWVMJGMVRQF-ROKXECAJSA-N 6-hydroxy-2,4,4-trimethyl-3-[(1e,3e,5e,7e,9e,11e,13e,15e,17e)-3,7,12,16-tetramethyl-18-(2,6,6-trimethyl-3-oxocyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-2-en-1-one Chemical compound CC=1C(=O)C(O)CC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)C(=O)CCC1(C)C OOUTWVMJGMVRQF-ROKXECAJSA-N 0.000 description 1
241000972773 Aulopiformes Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
FMKGDHLSXFDSOU-BDPUVYQTSA-N Dienon-Astacin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C(=O)C(=CC1(C)C)O)C=CC=C(/C)C=CC2=C(C)C(=O)C(=CC2(C)C)O FMKGDHLSXFDSOU-BDPUVYQTSA-N 0.000 description 1
102000002322 Egg Proteins Human genes 0.000 description 1
108010000912 Egg Proteins Proteins 0.000 description 1
UPYKUZBSLRQECL-UKMVMLAPSA-N Lycopene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(=C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=C)CCCC2(C)C UPYKUZBSLRQECL-UKMVMLAPSA-N 0.000 description 1
241000277331 Salmonidae Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000003929 acidic solution Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
238000009360 aquaculture Methods 0.000 description 1
244000144974 aquaculture Species 0.000 description 1
RASZIXQTZOARSV-QISQUURKSA-N astacene Chemical compound CC=1C(=O)C(=O)CC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)C(=O)C(=O)CC1(C)C RASZIXQTZOARSV-QISQUURKSA-N 0.000 description 1
150000001514 astaxanthins Chemical class 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
DKSMCEUSSQTGBK-UHFFFAOYSA-N bromous acid Chemical compound OBr=O DKSMCEUSSQTGBK-UHFFFAOYSA-N 0.000 description 1
244000309464 bull Species 0.000 description 1
235000005473 carotenes Nutrition 0.000 description 1
239000007810 chemical reaction solvent Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
235000013345 egg yolk Nutrition 0.000 description 1
210000002969 egg yolk Anatomy 0.000 description 1
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
230000019612 pigmentation Effects 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
235000019515 salmon Nutrition 0.000 description 1
239000002002 slurry Substances 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
235000010262 sodium metabisulphite Nutrition 0.000 description 1
239000004296 sodium metabisulphite Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
238000000844 transformation Methods 0.000 description 1
238000007738 vacuum evaporation Methods 0.000 description 1
NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

NO20024266A 2001-09-13 2002-09-06 Fremstilling av 4,4'-diketo beta-karotenderivater NO328027B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US09/953,007 US6372946B1 (en)	2001-09-13	2001-09-13	Preparation of 4,4′-diketo-β-carotene derivatives

Publications (3)

Publication Number	Publication Date
NO20024266D0 NO20024266D0 (no)	2002-09-06
NO20024266L NO20024266L (no)	2003-03-14
NO328027B1 true NO328027B1 (no)	2009-11-10

Family

ID=25493453

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20024266A NO328027B1 (no)	2001-09-13	2002-09-06	Fremstilling av 4,4'-diketo beta-karotenderivater

Country Status (11)

Country	Link
US (1)	US6372946B1 (es)
EP (1)	EP1293499B1 (es)
CN (1)	CN100396664C (es)
AT (1)	ATE319681T1 (es)
DE (1)	DE60209655T2 (es)
ES (1)	ES2258598T3 (es)
IL (1)	IL151586A (es)
MX (1)	MXPA02008914A (es)
NO (1)	NO328027B1 (es)
PE (1)	PE20030389A1 (es)
ZA (1)	ZA200207320B (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6372946B1 (en) *	2001-09-13	2002-04-16	Prodemex, S.A. De C.V.	Preparation of 4,4′-diketo-β-carotene derivatives
DE10225856A1 (de) *	2002-06-11	2004-01-08	Degussa Ag	Verfahren zur Herstellung von Canthaxanthin
CA2496207A1 (en) *	2002-08-20	2004-03-04	Sungene Gmbh & Co. Kgaa	Method for the production of zeaxanthin and/or the biosynthetic intermediates and/or subsequent products thereof
WO2004039991A2 (en) *	2002-10-25	2004-05-13	Prodemex, S.A. De C.V.	Method for producing esterified astaxanthin from esterified zeaxanthin
ES2223270B1 (es) *	2003-04-10	2006-04-16	Carotenoid Technologies, S.A.	Procedimiento para la sintesis de astaxantina.
KR101019787B1 (ko)	2003-12-23	2011-03-04	구상호	칸타잔틴의 제조방법
JP2008506732A (ja) *	2004-07-21	2008-03-06	ディーエスエムアイピーアセッツビー．ブイ．	４−ケトルテインの調製および食品添加剤としての使用
ES2299305B1 (es) *	2005-07-29	2009-04-01	Carotenoid Technologies, S.A.	Procedimiento para la preparacion de astaxantina.
ES2299304B1 (es) *	2005-07-29	2009-04-01	Carotenoid Technologies, S.A.	Procedimiento para la preparacion de astaxantina.
CN105777599A (zh) *	2014-12-26	2016-07-20	上虞新和成生物化工有限公司	一种氧化法制备斑蝥黄的方法
CN109369486B (zh) *	2018-12-18	2020-06-23	厦门金达威维生素有限公司	一种斑蝥黄的制备方法
CN115057805B (zh) *	2022-05-16	2024-10-18	万华化学集团股份有限公司	一种高全反式异构体稳定性角黄素晶体的方法
CN115073340B (zh) *	2022-06-28	2024-04-09	万华化学集团股份有限公司	一种角黄素的合成方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1058626A (en) *	1975-08-05	1979-07-17	Joachim Paust	Manufacture of canthaxanthin
JP3387554B2 (ja) *	1993-06-11	2003-03-17	新日本石油株式会社	カンタキサンチンの製造方法
DE4322277A1 (de) *	1993-07-05	1995-01-12	Basf Ag	Verbessertes Verfahren zur Herstellung von Astaxanthin, neue Zwischenprodukte hierfür sowie ein Verfahren zu deren Herstellung
JP2000351763A (ja) *	1999-06-09	2000-12-19	Kuraray Co Ltd	カンタキサンチンの製造方法
US6376717B2 (en) *	2000-04-26	2002-04-23	Prodemex, S.A. De C.V.	Preparation of astaxanthin
US6372946B1 (en) *	2001-09-13	2002-04-16	Prodemex, S.A. De C.V.	Preparation of 4,4′-diketo-β-carotene derivatives

2001
- 2001-09-13 US US09/953,007 patent/US6372946B1/en not_active Expired - Lifetime
2002
- 2002-09-03 IL IL151586A patent/IL151586A/en not_active IP Right Cessation
- 2002-09-06 CN CNB021416206A patent/CN100396664C/zh not_active Expired - Fee Related
- 2002-09-06 NO NO20024266A patent/NO328027B1/no not_active IP Right Cessation
- 2002-09-09 ES ES02256236T patent/ES2258598T3/es not_active Expired - Lifetime
- 2002-09-09 AT AT02256236T patent/ATE319681T1/de not_active IP Right Cessation
- 2002-09-09 EP EP02256236A patent/EP1293499B1/en not_active Expired - Lifetime
- 2002-09-09 DE DE60209655T patent/DE60209655T2/de not_active Expired - Lifetime
- 2002-09-12 MX MXPA02008914A patent/MXPA02008914A/es active IP Right Grant
- 2002-09-12 ZA ZA200207320A patent/ZA200207320B/xx unknown
- 2002-09-13 PE PE2002000906A patent/PE20030389A1/es not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE60209655D1 (de)	2006-05-04
CN100396664C (zh)	2008-06-25
NO20024266L (no)	2003-03-14
CN1417207A (zh)	2003-05-14
PE20030389A1 (es)	2003-06-13
ES2258598T3 (es)	2006-09-01
ZA200207320B (en)	2003-05-12
DE60209655T2 (de)	2006-10-05
EP1293499B1 (en)	2006-03-08
MXPA02008914A (es)	2004-08-19
IL151586A0 (en)	2003-04-10
EP1293499A1 (en)	2003-03-19
ATE319681T1 (de)	2006-03-15
IL151586A (en)	2007-06-03
NO20024266D0 (no)	2002-09-06
US6372946B1 (en)	2002-04-16

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