NO328027B1 - Fremstilling av 4,4'-diketo beta-karotenderivater - Google Patents
Fremstilling av 4,4'-diketo beta-karotenderivater Download PDFInfo
- Publication number
- NO328027B1 NO328027B1 NO20024266A NO20024266A NO328027B1 NO 328027 B1 NO328027 B1 NO 328027B1 NO 20024266 A NO20024266 A NO 20024266A NO 20024266 A NO20024266 A NO 20024266A NO 328027 B1 NO328027 B1 NO 328027B1
- Authority
- NO
- Norway
- Prior art keywords
- carotene
- sodium
- potassium
- derivatives
- bromate
- Prior art date
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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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 (de) |
| EP (1) | EP1293499B1 (de) |
| CN (1) | CN100396664C (de) |
| AT (1) | ATE319681T1 (de) |
| DE (1) | DE60209655T2 (de) |
| ES (1) | ES2258598T3 (de) |
| IL (1) | IL151586A (de) |
| MX (1) | MXPA02008914A (de) |
| NO (1) | NO328027B1 (de) |
| PE (1) | PE20030389A1 (de) |
| ZA (1) | ZA200207320B (de) |
Families Citing this family (13)
| 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 |
| US20070094749A1 (en) * | 2002-08-20 | 2007-04-26 | Sungene Gmbh & Co. Kgaa | Method for producing ketocarotinoids in plant fruit |
| EP1563081A4 (de) * | 2002-10-25 | 2005-10-26 | Verfahren zur herstellung von verestertem astaxanthin aus verestertem 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 |
| MX2007000797A (es) * | 2004-07-21 | 2007-04-09 | Dsm Ip Assets Bv | Preparacion de 4-cetoluteina y su uso como aditivo alimenticio. |
| 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 |
| CN115057805A (zh) * | 2022-05-16 | 2022-09-16 | 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)
| 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 NO NO20024266A patent/NO328027B1/no not_active IP Right Cessation
- 2002-09-06 CN CNB021416206A patent/CN100396664C/zh not_active Expired - Fee Related
- 2002-09-09 ES ES02256236T patent/ES2258598T3/es not_active Expired - Lifetime
- 2002-09-09 EP EP02256236A patent/EP1293499B1/de not_active Expired - Lifetime
- 2002-09-09 DE DE60209655T patent/DE60209655T2/de not_active Expired - Lifetime
- 2002-09-09 AT AT02256236T patent/ATE319681T1/de not_active IP Right Cessation
- 2002-09-12 ZA ZA200207320A patent/ZA200207320B/xx unknown
- 2002-09-12 MX MXPA02008914A patent/MXPA02008914A/es active IP Right Grant
- 2002-09-13 PE PE2002000906A patent/PE20030389A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20024266D0 (no) | 2002-09-06 |
| ATE319681T1 (de) | 2006-03-15 |
| US6372946B1 (en) | 2002-04-16 |
| IL151586A0 (en) | 2003-04-10 |
| PE20030389A1 (es) | 2003-06-13 |
| ZA200207320B (en) | 2003-05-12 |
| CN1417207A (zh) | 2003-05-14 |
| DE60209655T2 (de) | 2006-10-05 |
| EP1293499A1 (de) | 2003-03-19 |
| DE60209655D1 (de) | 2006-05-04 |
| NO20024266L (no) | 2003-03-14 |
| CN100396664C (zh) | 2008-06-25 |
| MXPA02008914A (es) | 2004-08-19 |
| ES2258598T3 (es) | 2006-09-01 |
| EP1293499B1 (de) | 2006-03-08 |
| IL151586A (en) | 2007-06-03 |
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| Date | Code | Title | Description |
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| CREP | Change of representative |
Representative=s name: ZACCO NORWAY AS, POSTBOKS 2003 VIKA, 0125 OSLO, NO |
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| MM1K | Lapsed by not paying the annual fees |