JPH036139B2 - - Google Patents
Info
- Publication number
- JPH036139B2 JPH036139B2 JP57192674A JP19267482A JPH036139B2 JP H036139 B2 JPH036139 B2 JP H036139B2 JP 57192674 A JP57192674 A JP 57192674A JP 19267482 A JP19267482 A JP 19267482A JP H036139 B2 JPH036139 B2 JP H036139B2
- Authority
- JP
- Japan
- Prior art keywords
- abscisic acid
- cis
- trans
- resin
- organic solvent
- Prior art date
- 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.)
- Expired - Lifetime
Links
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 claims description 86
- FCRACOPGPMPSHN-UHFFFAOYSA-N desoxyabscisic acid Natural products OC(=O)C=C(C)C=CC1C(C)=CC(=O)CC1(C)C FCRACOPGPMPSHN-UHFFFAOYSA-N 0.000 claims description 43
- 239000003960 organic solvent Substances 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- 239000003957 anion exchange resin Substances 0.000 claims description 9
- 239000003480 eluent Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 239000004793 Polystyrene Substances 0.000 claims description 8
- 229920002223 polystyrene Polymers 0.000 claims description 8
- 238000001179 sorption measurement Methods 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000010828 elution Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 15
- 239000000047 product Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 241001064001 Rosisphaerella rosicola Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000001965 potato dextrose agar Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920001429 chelating resin Polymers 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000011218 seed culture Methods 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- -1 ~2N Substances 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- 241000351221 Alternaria rosicola Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003375 plant hormone Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19267482A JPS5982340A (ja) | 1982-11-02 | 1982-11-02 | アブサイジン酸の精製法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19267482A JPS5982340A (ja) | 1982-11-02 | 1982-11-02 | アブサイジン酸の精製法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5982340A JPS5982340A (ja) | 1984-05-12 |
JPH036139B2 true JPH036139B2 (cs) | 1991-01-29 |
Family
ID=16295150
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19267482A Granted JPS5982340A (ja) | 1982-11-02 | 1982-11-02 | アブサイジン酸の精製法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5982340A (cs) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04202176A (ja) * | 1990-11-29 | 1992-07-22 | Toray Ind Inc | アブシジン酸の精製法 |
CN1306035C (zh) * | 2004-09-14 | 2007-03-21 | 中国科学院成都生物研究所 | 一种天然脱落酸的提取方法 |
JP2007222203A (ja) * | 2006-02-21 | 2007-09-06 | Sumida Corporation | ミラー駆動機構およびこのミラー駆動機構を具備する撮像装置 |
CN116730831B (zh) * | 2023-07-03 | 2024-04-12 | 江西新瑞丰生化股份有限公司 | 一种脱落酸母液的提取方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56160996A (en) * | 1980-05-15 | 1981-12-11 | Kyowa Hakko Kogyo Co Ltd | Preparation of abscisic acid by fermentation method |
-
1982
- 1982-11-02 JP JP19267482A patent/JPS5982340A/ja active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56160996A (en) * | 1980-05-15 | 1981-12-11 | Kyowa Hakko Kogyo Co Ltd | Preparation of abscisic acid by fermentation method |
Also Published As
Publication number | Publication date |
---|---|
JPS5982340A (ja) | 1984-05-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4861870A (en) | Process for purifying anthracyclinone glycosides by selective adsorption on resins | |
EP2402306B1 (en) | Method for producing 5-aminolevulinic acid hydrochloride | |
SK832006A3 (sk) | Spôsob izolácie polymyxínu B z vyfermentovanej pôdy | |
US5986089A (en) | Process for the preparation of moenomycin A | |
JPH036139B2 (cs) | ||
JP2001258583A (ja) | シキミ酸の精製方法 | |
JP3421338B2 (ja) | バンコマイシンの製造方法 | |
US5258495A (en) | Process for making vancomycin HC1 | |
US4515943A (en) | Crystal of beta-nicotinamide-adenine-dinucleotide and process for preparing the same | |
US5180670A (en) | Method for purification of mitomycin C | |
CN113511967B (zh) | 一种从银杏叶提取物层析废水中提取奎宁酸的方法 | |
JP3382297B2 (ja) | 高純度デフェロキサミン塩の製造法 | |
JPH07165702A (ja) | 天然型アブシジン酸の単離方法 | |
JP2971128B2 (ja) | マイトマイシンcの精製法 | |
US5026640A (en) | Process for the conversion of corrinoids produced by microorganisms into cyanocorrinoids | |
JPS6337635B2 (cs) | ||
EP0009363A1 (en) | Method of separating cephalosporins | |
JPH04202176A (ja) | アブシジン酸の精製法 | |
JPS6216497A (ja) | シチジン―5′―ジリン酸コリン1水和物結晶の製造法 | |
RU1822885C (ru) | Способ выделени 4-и/или 5-оксииндолил-3-уксусных кислот | |
KR840002477B1 (ko) | 세파로스포린류의 분리법 | |
US2677644A (en) | Purification of vitamin b12 solutions | |
JPS62293A (ja) | L−ラムノ−スの製造法 | |
JPH0776570A (ja) | アブシジン酸の単離方法 | |
GB2180538A (en) | Process for the separation of corrinoids |