CN101270135A - 从茶叶提取物-含咖啡因茶多酚中脱除咖啡因的方法 - Google Patents
从茶叶提取物-含咖啡因茶多酚中脱除咖啡因的方法 Download PDFInfo
- Publication number
- CN101270135A CN101270135A CNA2008100251610A CN200810025161A CN101270135A CN 101270135 A CN101270135 A CN 101270135A CN A2008100251610 A CNA2008100251610 A CN A2008100251610A CN 200810025161 A CN200810025161 A CN 200810025161A CN 101270135 A CN101270135 A CN 101270135A
- Authority
- CN
- China
- Prior art keywords
- tea
- caffeine
- polyphenol
- ethyl acetate
- acetate solution
- 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.)
- Granted
Links
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 title claims abstract description 183
- 238000000034 method Methods 0.000 title claims abstract description 32
- 241001122767 Theaceae Species 0.000 title claims abstract 7
- 239000000284 extract Substances 0.000 title abstract description 11
- 235000013824 polyphenols Nutrition 0.000 title abstract description 10
- 150000008442 polyphenolic compounds Chemical class 0.000 title abstract description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 118
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 claims abstract description 88
- 229960001948 caffeine Drugs 0.000 claims abstract description 88
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims abstract description 88
- 239000011973 solid acid Substances 0.000 claims abstract description 29
- 239000000047 product Substances 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 238000010521 absorption reaction Methods 0.000 claims description 11
- 238000001914 filtration Methods 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- 229940045641 monobasic sodium phosphate Drugs 0.000 claims description 5
- 239000000741 silica gel Substances 0.000 claims description 5
- 229910002027 silica gel Inorganic materials 0.000 claims description 5
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 238000001179 sorption measurement Methods 0.000 claims description 4
- 239000000706 filtrate Substances 0.000 claims description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 2
- 150000008107 benzenesulfonic acids Chemical class 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 230000009977 dual effect Effects 0.000 claims description 2
- 238000003810 ethyl acetate extraction Methods 0.000 claims description 2
- 238000005342 ion exchange Methods 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000002904 solvent Substances 0.000 abstract description 9
- 239000000843 powder Substances 0.000 abstract description 6
- 235000019804 chlorophyll Nutrition 0.000 abstract description 4
- 238000000926 separation method Methods 0.000 abstract description 4
- 230000000274 adsorptive effect Effects 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 244000269722 Thea sinensis Species 0.000 description 6
- WMBWREPUVVBILR-WIYYLYMNSA-N (-)-Epigallocatechin-3-o-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-WIYYLYMNSA-N 0.000 description 5
- WMBWREPUVVBILR-UHFFFAOYSA-N GCG Natural products C=1C(O)=C(O)C(O)=CC=1C1OC2=CC(O)=CC(O)=C2CC1OC(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 230000002572 peristaltic effect Effects 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 229960001866 silicon dioxide Drugs 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 229930002875 chlorophyll Natural products 0.000 description 3
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- UGAPHEBNTGUMBB-UHFFFAOYSA-N acetic acid;ethyl acetate Chemical compound CC(O)=O.CCOC(C)=O UGAPHEBNTGUMBB-UHFFFAOYSA-N 0.000 description 2
- 230000001093 anti-cancer Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 2
- 235000005487 catechin Nutrition 0.000 description 2
- 229950001002 cianidanol Drugs 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000002024 ethyl acetate extract Substances 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 230000001473 noxious effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- NFIYTPYOYDDLGO-UHFFFAOYSA-N phosphoric acid;sodium Chemical compound [Na].OP(O)(O)=O NFIYTPYOYDDLGO-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- 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
- LCCDINSFSOALJK-UHFFFAOYSA-N 1,3,4-trimethylpurine-2,6-dione Chemical compound O=C1N(C)C(=O)N(C)C2(C)N=CN=C21 LCCDINSFSOALJK-UHFFFAOYSA-N 0.000 description 1
- QCOZYUGXYJSINC-UHFFFAOYSA-N 1,3,7-trimethylpurine-2,6-dione Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C.CN1C(=O)N(C)C(=O)C2=C1N=CN2C QCOZYUGXYJSINC-UHFFFAOYSA-N 0.000 description 1
- RTAPDZBZLSXHQQ-UHFFFAOYSA-N 8-methyl-3,7-dihydropurine-2,6-dione Chemical class N1C(=O)NC(=O)C2=C1N=C(C)N2 RTAPDZBZLSXHQQ-UHFFFAOYSA-N 0.000 description 1
- 206010059313 Anogenital warts Diseases 0.000 description 1
- 208000000907 Condylomata Acuminata Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000701806 Human papillomavirus Species 0.000 description 1
- 229930012538 Paclitaxel Natural products 0.000 description 1
- 240000003152 Rhus chinensis Species 0.000 description 1
- 235000014220 Rhus chinensis Nutrition 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 150000003797 alkaloid derivatives Chemical class 0.000 description 1
- LNTHITQWFMADLM-UHFFFAOYSA-N anhydrous gallic acid Natural products OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
- 208000025009 anogenital human papillomavirus infection Diseases 0.000 description 1
- 201000004201 anogenital venereal wart Diseases 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- -1 catechin gallic acid ester Chemical class 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940030275 epigallocatechin gallate Drugs 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 230000002218 hypoglycaemic effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- 235000012054 meals Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000011275 oncology therapy Methods 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 229960001592 paclitaxel Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000000955 prescription drug Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000004223 radioprotective effect Effects 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 238000003815 supercritical carbon dioxide extraction Methods 0.000 description 1
- 238000000194 supercritical-fluid extraction Methods 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
Landscapes
- Tea And Coffee (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
Claims (2)
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CN2008100251610A CN101270135B (zh) | 2008-04-24 | 2008-04-24 | 从茶叶提取物—含咖啡因茶多酚中脱除咖啡因的方法 |
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CN2008100251610A CN101270135B (zh) | 2008-04-24 | 2008-04-24 | 从茶叶提取物—含咖啡因茶多酚中脱除咖啡因的方法 |
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CN101270135A true CN101270135A (zh) | 2008-09-24 |
CN101270135B CN101270135B (zh) | 2011-04-20 |
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CN2008100251610A Expired - Fee Related CN101270135B (zh) | 2008-04-24 | 2008-04-24 | 从茶叶提取物—含咖啡因茶多酚中脱除咖啡因的方法 |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102225122A (zh) * | 2011-06-09 | 2011-10-26 | 四川中测科技投资有限公司 | 无咖啡因茶多酚及其制备方法 |
CN102875691A (zh) * | 2012-10-19 | 2013-01-16 | 黄冈师范学院 | 一种从茶渣中同步制备多种活性物质的方法 |
CN104886306A (zh) * | 2014-03-07 | 2015-09-09 | 上海强圣医药科技有限公司 | 精制脱咖啡因egcg及制备脱咖啡因egcg茶颗粒的方法 |
CN105746786A (zh) * | 2016-03-21 | 2016-07-13 | 信阳农林学院 | 一种低咖啡因、高可溶性糖翅柃茶的制备方法 |
CN106581308A (zh) * | 2017-01-03 | 2017-04-26 | 花园药业股份有限公司 | 一种用于心脑健的茶叶提取物的制备方法 |
CN107913530A (zh) * | 2017-11-24 | 2018-04-17 | 广西中港高科国宝金花茶产业有限公司 | 一种co2超临界法流体从金花茶萃取出茶多酚的方法 |
CN107954968A (zh) * | 2017-11-16 | 2018-04-24 | 华南师范大学 | 一种简单高效的双液相提取、分离纯化和制备高纯度茶多酚的方法 |
CN110129169A (zh) * | 2019-05-22 | 2019-08-16 | 遵义医科大学 | 降低蒸馏型茶酒中咖啡因含量的方法 |
CN111840410A (zh) * | 2020-07-28 | 2020-10-30 | 上海科德实业有限公司 | 从茶叶中提取高纯茶多酚方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100379732C (zh) * | 2006-02-28 | 2008-04-09 | 浙江大学 | 从茶多酚粗提物中脱去咖啡因的方法 |
CN100496272C (zh) * | 2006-05-08 | 2009-06-10 | 浙江经贸职业技术学院 | 从茶叶中脱去咖啡碱的方法 |
-
2008
- 2008-04-24 CN CN2008100251610A patent/CN101270135B/zh not_active Expired - Fee Related
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102225122A (zh) * | 2011-06-09 | 2011-10-26 | 四川中测科技投资有限公司 | 无咖啡因茶多酚及其制备方法 |
CN102875691A (zh) * | 2012-10-19 | 2013-01-16 | 黄冈师范学院 | 一种从茶渣中同步制备多种活性物质的方法 |
CN104886306A (zh) * | 2014-03-07 | 2015-09-09 | 上海强圣医药科技有限公司 | 精制脱咖啡因egcg及制备脱咖啡因egcg茶颗粒的方法 |
CN105746786A (zh) * | 2016-03-21 | 2016-07-13 | 信阳农林学院 | 一种低咖啡因、高可溶性糖翅柃茶的制备方法 |
CN105746786B (zh) * | 2016-03-21 | 2019-08-06 | 信阳农林学院 | 一种低咖啡因、高可溶性糖翅柃茶的制备方法 |
CN106581308A (zh) * | 2017-01-03 | 2017-04-26 | 花园药业股份有限公司 | 一种用于心脑健的茶叶提取物的制备方法 |
CN106581308B (zh) * | 2017-01-03 | 2020-11-17 | 花园药业股份有限公司 | 一种用于心脑健片和胶囊的茶叶提取物的制备方法 |
CN107954968A (zh) * | 2017-11-16 | 2018-04-24 | 华南师范大学 | 一种简单高效的双液相提取、分离纯化和制备高纯度茶多酚的方法 |
CN107954968B (zh) * | 2017-11-16 | 2021-04-30 | 华南师范大学 | 一种简单高效的双液相提取、分离纯化和制备高纯度茶多酚的方法 |
CN107913530A (zh) * | 2017-11-24 | 2018-04-17 | 广西中港高科国宝金花茶产业有限公司 | 一种co2超临界法流体从金花茶萃取出茶多酚的方法 |
CN110129169A (zh) * | 2019-05-22 | 2019-08-16 | 遵义医科大学 | 降低蒸馏型茶酒中咖啡因含量的方法 |
CN111840410A (zh) * | 2020-07-28 | 2020-10-30 | 上海科德实业有限公司 | 从茶叶中提取高纯茶多酚方法 |
Also Published As
Publication number | Publication date |
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CN101270135B (zh) | 2011-04-20 |
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Assignee: Xiangxi Autonomous Prefecture Orac Pharm & Chem Co., Ltd. Assignor: Chuntian Biotechnology Development Co., Ltd., Xiangxi Autonomous County Contract record no.: 2011430000063 Denomination of invention: From tea leaf extract-the contain method that removes caffeine the caffeine tea-polyphenol Granted publication date: 20110420 License type: Exclusive License Open date: 20080924 Record date: 20110509 |
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