ID19677A - Konversi xantofil - Google Patents
Konversi xantofilInfo
- Publication number
- ID19677A ID19677A IDP973289A ID973289A ID19677A ID 19677 A ID19677 A ID 19677A ID P973289 A IDP973289 A ID P973289A ID 973289 A ID973289 A ID 973289A ID 19677 A ID19677 A ID 19677A
- Authority
- ID
- Indonesia
- Prior art keywords
- lutein
- zeaxanthin
- integuments
- organic solvent
- conversion
- Prior art date
Links
- 238000006243 chemical reaction Methods 0.000 title abstract 2
- 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 abstract 7
- 235000012680 lutein Nutrition 0.000 abstract 4
- 239000001656 lutein Substances 0.000 abstract 4
- KBPHJBAIARWVSC-RGZFRNHPSA-N lutein 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=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C KBPHJBAIARWVSC-RGZFRNHPSA-N 0.000 abstract 4
- 229960005375 lutein Drugs 0.000 abstract 4
- ORAKUVXRZWMARG-WZLJTJAWSA-N lutein 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=CC2C(=CC(O)CC2(C)C)C ORAKUVXRZWMARG-WZLJTJAWSA-N 0.000 abstract 4
- FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll 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=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 abstract 4
- 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 abstract 3
- 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 abstract 3
- 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 abstract 3
- 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 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 235000010930 zeaxanthin Nutrition 0.000 abstract 3
- 239000001775 zeaxanthin Substances 0.000 abstract 3
- 229940043269 zeaxanthin Drugs 0.000 abstract 3
- 239000003960 organic solvent Substances 0.000 abstract 2
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 abstract 1
- 241000251468 Actinopterygii Species 0.000 abstract 1
- 241000238424 Crustacea Species 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- 102000002322 Egg Proteins Human genes 0.000 abstract 1
- 108010000912 Egg Proteins Proteins 0.000 abstract 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 235000021466 carotenoid Nutrition 0.000 abstract 1
- 150000001747 carotenoids Chemical class 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 235000013345 egg yolk Nutrition 0.000 abstract 1
- 210000002969 egg yolk Anatomy 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 238000006317 isomerization reaction Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003444 phase transfer catalyst Substances 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 230000019612 pigmentation Effects 0.000 abstract 1
- 244000144977 poultry Species 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 210000004003 subcutaneous fat Anatomy 0.000 abstract 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B61/00—Dyes of natural origin prepared from natural sources, e.g. vegetable sources
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)
- Steroid Compounds (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96115908 | 1996-10-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
ID19677A true ID19677A (id) | 1998-07-30 |
Family
ID=8223265
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IDP973289A ID19677A (id) | 1996-10-04 | 1997-09-25 | Konversi xantofil |
Country Status (8)
Country | Link |
---|---|
US (1) | US5780693A (id) |
JP (1) | JP3828252B2 (id) |
CN (1) | CN1082507C (id) |
AT (1) | ATE210166T1 (id) |
BR (1) | BR9704976A (id) |
DE (1) | DE59705649D1 (id) |
ES (1) | ES2167661T3 (id) |
ID (1) | ID19677A (id) |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5827652A (en) | 1995-10-31 | 1998-10-27 | Applied Food Biotechnology, Inc. | Zeaxanthin formulations for human ingestion |
US5998678A (en) * | 1997-02-25 | 1999-12-07 | Investigaciones Quimicas Y Farmaceutics, S.A. | Process for preparing carotenoid pigments |
EP0984915A4 (en) | 1997-04-04 | 2002-11-27 | Henkel Corp | LUTEINE ESTERS WITH HIGH BIOAVAILABILITY |
US5876782A (en) * | 1997-05-14 | 1999-03-02 | Kemin Industries, Inc. | Method for the conversion of xanthophylls in plant material |
PE130499A1 (es) * | 1997-10-31 | 1999-12-17 | Bioquimex Reka S A De C V | Procedimiento para la isomerizacion de luteina a zeaxantina y el producto obtenido con el mismo |
US6573299B1 (en) | 1999-09-20 | 2003-06-03 | Advanced Medical Instruments | Method and compositions for treatment of the aging eye |
US6504067B1 (en) * | 1999-11-24 | 2003-01-07 | Industrial Organica S.A. De C.V. | Process to obtain xanthophyll concentrates of high purity |
US6818798B1 (en) | 2000-05-03 | 2004-11-16 | University Of Maryland, College Park | Process for making a (3R,3′R)-zeaxanthin precursor |
US6420614B1 (en) * | 2000-10-10 | 2002-07-16 | Industrial Organica, S.A. De C.V. | Process for obtaining 3′-epilutein |
US7691406B2 (en) * | 2000-10-27 | 2010-04-06 | ZeaVision LLC. | Zeaxanthin formulations for human ingestion |
US6784351B2 (en) * | 2001-06-29 | 2004-08-31 | Ball Horticultural Company | Targetes erecta marigolds with altered carotenoid compositions and ratios |
US7173145B2 (en) * | 2001-11-29 | 2007-02-06 | University Of Maryland, College Park | Process for extraction and purification of lutein, zeaxanthin and rare carotenoids from marigold flowers and plants |
US8088363B2 (en) | 2002-10-28 | 2012-01-03 | Zeavision Llc | Protection against sunburn and skin problems with orally-ingested high-dosage zeaxanthin |
US9192586B2 (en) | 2003-03-10 | 2015-11-24 | Zeavision Llc | Zeaxanthin formulations with additional ocular-active nutrients, for protecting eye health and treating eye disorders |
US20070082066A1 (en) * | 2003-05-07 | 2007-04-12 | Gierhart Dennis L | Use of zeaxanthin to reduce light hyper-sensitivity, photophobia, and medical conditions relating to light hyper-sensitivity |
DE10349455A1 (de) * | 2003-10-23 | 2005-05-25 | Bioghurt Biogarde Gmbh & Co. Kg | Verfahren zur Herstellung konjugierter, mehrfach ungesättigter Fettsäureester |
US7941211B2 (en) * | 2003-11-17 | 2011-05-10 | Zeavision, Llc. | Preloading with macular pigment to improve photodynamic treatment of retinal vascular disorders |
US7351424B2 (en) * | 2004-07-22 | 2008-04-01 | Bio Lut S.A. De C.V. | Enhanced purity trans-lutein-ester compositions and methods of making same |
US20060089411A1 (en) * | 2004-08-07 | 2006-04-27 | Gierhart Dennis L | Treatment of Stargardt's disease and other lipofuscin disorders with combined retinaldehyde inhibitor and zeaxanthin |
US20070065487A1 (en) * | 2005-09-21 | 2007-03-22 | Bio Lut S.A. De C.V. | Trans-lutein xantophyll ester of high purity and high bioavailability in micellar solution and a process for the preparation thereof |
AT503329A1 (de) * | 2006-03-02 | 2007-09-15 | Omnica Gmbh | Verfahren zur herstellung einer zusammensetzung, welche zumindest ein xantophyll enthält |
US8212063B2 (en) * | 2006-05-10 | 2012-07-03 | Omniactive Health Technologies Limited | Xanthophyll composition containing trans, meso-zeaxanthin, trans, R, R-zeaxanthin and trans, R, R-lutein useful for nutrition and health care and a process for its preparation |
US7282225B1 (en) | 2006-09-27 | 2007-10-16 | Occular Technologies, Inc. | Composition and methods for improving retinal health |
CN101153017B (zh) * | 2006-09-28 | 2010-12-22 | 浙江医药股份有限公司新昌制药厂 | 高含量食用级玉米黄质的制备方法 |
WO2009019712A1 (en) * | 2007-08-03 | 2009-02-12 | Omniactive Health Technologies Pvt Ltd. | Novel xanthophyll composition contaning (trans, meso) - zeaxanthin, and a process for its preparation |
US8093436B2 (en) * | 2008-03-19 | 2012-01-10 | University Of Maryland, College Park | Process for synthesis of (3R,3′R)-zeaxanthin and (3R,3′S;meso)-zeaxanthin from (3R,3′R,6′R)-lutein via (3R)-3′,4′-anhydrolutein |
WO2011027209A1 (en) * | 2009-09-02 | 2011-03-10 | Omniactive Health Technologies Ltd. | A xanthophyl composition containing macular pigments and a process for its preparation |
CN101781240B (zh) * | 2010-01-07 | 2014-06-04 | 浙江医药股份有限公司新昌制药厂 | 一种以植物油树脂为原料制备含较高玉米黄质含量的叶黄素晶体的方法 |
JP2014529607A (ja) | 2011-08-26 | 2014-11-13 | ピーティーティー グローバル ケミカル パブリック カンパニー リミテッド | 天然物質からルテイン/キサントフィルを抽出する方法、並びにこの方法により得られる高度精製ルテイン/キサントフィル |
CN102399178A (zh) * | 2011-10-29 | 2012-04-04 | 南昌大学 | 一种由叶黄素酯一锅法转化为玉米黄素的方法 |
CN102746203B (zh) * | 2012-07-12 | 2014-08-27 | 浙江医药股份有限公司新昌制药厂 | 一种高含量玉米黄素的制备方法 |
CN102757373B (zh) * | 2012-07-31 | 2014-03-19 | 沈阳天峰生物制药有限公司 | 一种由万寿菊花粒制备高纯度叶黄素酯的方法 |
CN105399653B (zh) * | 2014-08-27 | 2017-10-10 | 浙江医药股份有限公司新昌制药厂 | 一种由万寿菊油树脂一步法制备玉米黄素的工业化方法 |
CN104447469B (zh) * | 2014-12-08 | 2016-08-17 | 晨光生物科技集团股份有限公司 | 叶黄素浸膏高效制备玉米黄质的方法 |
CN106316908B (zh) * | 2015-06-30 | 2018-02-13 | 上虞新和成生物化工有限公司 | 一种高纯度虾青素的合成方法 |
CN105085351A (zh) * | 2015-09-22 | 2015-11-25 | 哈尔滨宝德生物技术股份有限公司 | 叶黄素转化玉米黄质的工艺 |
CN106977439B (zh) * | 2017-03-23 | 2018-10-02 | 广州智特奇生物科技股份有限公司 | 一种叶黄素的异构化方法 |
CN111548294A (zh) * | 2020-04-10 | 2020-08-18 | 天津大学 | 一种叶黄素甲醇溶剂化物晶体及其制备方法 |
CN114957072A (zh) * | 2021-02-25 | 2022-08-30 | 内蒙古昶辉生物科技股份有限公司 | 由万寿菊油膏制备玉米黄质以及玉米黄质微丸的方法 |
CN114369050B (zh) * | 2022-01-21 | 2023-08-25 | 山东天音生物科技有限公司 | 一种叶黄素酯的制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1046658A (en) * | 1964-03-19 | 1966-10-26 | Kodak Ltd | Improvements in pigmenting activity of xanthophyll |
US3523138A (en) * | 1965-03-01 | 1970-08-04 | Eastman Kodak Co | Treatment of marigold petal meal to obtain a xanthophyll product |
NL6610613A (id) * | 1966-07-28 | 1968-01-29 | ||
US3783099A (en) * | 1971-11-08 | 1974-01-01 | Ralston Purina Co | Xanthophyllic extraction process |
JPH0848895A (ja) * | 1994-03-28 | 1996-02-20 | Leonardo Espinosa Sanchez Roberto | センパスチルの花の粉末、オレオレジン、又は同花から作られた他の形態の物に含まれる人および動物用の色素鹸化及び獲得における改良 |
US5523494A (en) * | 1994-07-20 | 1996-06-04 | Industrial Organica, S.A. De C.V. | Process for the isomerization of lutein |
ES2107391B1 (es) * | 1996-02-27 | 1998-06-16 | Invest Quimicas Y Farmaceutica | Procedimiento para la preparacion de carotenoides y pigmentos que los contienen. |
-
1997
- 1997-09-04 CN CN97117598A patent/CN1082507C/zh not_active Expired - Fee Related
- 1997-09-22 US US08/935,262 patent/US5780693A/en not_active Expired - Lifetime
- 1997-09-25 ID IDP973289A patent/ID19677A/id unknown
- 1997-09-30 DE DE59705649T patent/DE59705649D1/de not_active Expired - Lifetime
- 1997-09-30 ES ES97116944T patent/ES2167661T3/es not_active Expired - Lifetime
- 1997-09-30 AT AT97116944T patent/ATE210166T1/de not_active IP Right Cessation
- 1997-10-02 JP JP26953997A patent/JP3828252B2/ja not_active Expired - Fee Related
- 1997-10-03 BR BR9704976A patent/BR9704976A/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH10114739A (ja) | 1998-05-06 |
BR9704976A (pt) | 1999-07-20 |
ES2167661T3 (es) | 2002-05-16 |
JP3828252B2 (ja) | 2006-10-04 |
CN1178787A (zh) | 1998-04-15 |
DE59705649D1 (de) | 2002-01-17 |
US5780693A (en) | 1998-07-14 |
ATE210166T1 (de) | 2001-12-15 |
CN1082507C (zh) | 2002-04-10 |
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