SK115399A3 - Process for the preparation of stable, non-hygroscopic salts of l(-)carnitine and alkanoyl l(-)carnitines - Google Patents
Process for the preparation of stable, non-hygroscopic salts of l(-)carnitine and alkanoyl l(-)carnitines Download PDFInfo
- Publication number
- SK115399A3 SK115399A3 SK1153-99A SK115399A SK115399A3 SK 115399 A3 SK115399 A3 SK 115399A3 SK 115399 A SK115399 A SK 115399A SK 115399 A3 SK115399 A3 SK 115399A3
- Authority
- SK
- Slovakia
- Prior art keywords
- carnitine
- dryer
- amount
- salt
- reaction mixture
- Prior art date
Links
- PHIQHXFUZVPYII-UHFFFAOYSA-N carnitine Chemical class C[N+](C)(C)CC(O)CC([O-])=O PHIQHXFUZVPYII-UHFFFAOYSA-N 0.000 title claims abstract description 43
- 150000003839 salts Chemical class 0.000 title claims abstract description 28
- 238000000034 method Methods 0.000 title claims abstract description 17
- 125000001589 carboacyl group Chemical class 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title description 3
- 238000004519 manufacturing process Methods 0.000 claims description 15
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 10
- 238000007711 solidification Methods 0.000 claims description 9
- 230000008023 solidification Effects 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 8
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 7
- 230000018044 dehydration Effects 0.000 claims description 7
- 238000006297 dehydration reaction Methods 0.000 claims description 7
- 239000010802 sludge Substances 0.000 claims description 6
- 239000002002 slurry Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 5
- 239000001530 fumaric acid Substances 0.000 claims description 4
- 239000008187 granular material Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 2
- 235000011837 pasties Nutrition 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 8
- 239000007787 solid Substances 0.000 abstract description 5
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical group C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 abstract description 4
- DSLZVSRJTYRBFB-UHFFFAOYSA-N Galactaric acid Natural products OC(=O)C(O)C(O)C(O)C(O)C(O)=O DSLZVSRJTYRBFB-UHFFFAOYSA-N 0.000 abstract 2
- DSLZVSRJTYRBFB-DUHBMQHGSA-N galactaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O DSLZVSRJTYRBFB-DUHBMQHGSA-N 0.000 abstract 2
- 235000002639 sodium chloride Nutrition 0.000 description 22
- 239000000047 product Substances 0.000 description 9
- 235000005911 diet Nutrition 0.000 description 5
- 230000000378 dietary effect Effects 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 235000015872 dietary supplement Nutrition 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 241000251468 Actinopterygii Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 229960004203 carnitine Drugs 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 229940095064 tartrate Drugs 0.000 description 2
- VOTPLFCPIRIALF-UHFFFAOYSA-N 3-(2,4-dioxo-1h-pyrimidine-6-carbonyl)oxy-4-(trimethylazaniumyl)butanoate Chemical compound C[N+](C)(C)CC(CC([O-])=O)OC(=O)C1=CC(=O)NC(=O)N1 VOTPLFCPIRIALF-UHFFFAOYSA-N 0.000 description 1
- 241000777300 Congiopodidae Species 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 208000019914 Mental Fatigue Diseases 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 229960000678 carnitine chloride Drugs 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000015218 chewing gum Nutrition 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 235000001497 healthy food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 235000021075 protein intake Nutrition 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 210000002027 skeletal muscle Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 230000036642 wellbeing Effects 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/18—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/235—Saturated compounds containing more than one carboxyl group
- C07C59/245—Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
- C07C59/285—Polyhydroxy dicarboxylic acids having five or more carbon atoms, e.g. saccharic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT97MI000409A IT1289974B1 (it) | 1997-02-25 | 1997-02-25 | Procedimento per la produzione di sali stabili e non igroscopici di l(-)carnitina e di alcanoli l(-)-carnitine |
| PCT/EP1998/001039 WO1998038157A1 (en) | 1997-02-25 | 1998-02-24 | Process for the preparation of stable, non-hygroscopic salts of l(-)carnitine and alkanoyl l(-)carnitines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK115399A3 true SK115399A3 (en) | 2000-01-18 |
Family
ID=11376175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1153-99A SK115399A3 (en) | 1997-02-25 | 1998-02-24 | Process for the preparation of stable, non-hygroscopic salts of l(-)carnitine and alkanoyl l(-)carnitines |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US6271258B1 (zh) |
| EP (1) | EP1019362B1 (zh) |
| JP (1) | JP2001513096A (zh) |
| KR (1) | KR100538788B1 (zh) |
| CN (1) | CN1248967A (zh) |
| AT (1) | ATE222233T1 (zh) |
| AU (1) | AU724276B2 (zh) |
| BR (1) | BR9807761A (zh) |
| CA (1) | CA2281630C (zh) |
| CZ (1) | CZ290893B6 (zh) |
| DE (1) | DE69807245T2 (zh) |
| DK (1) | DK1019362T3 (zh) |
| EE (1) | EE03561B1 (zh) |
| ES (1) | ES2182290T3 (zh) |
| HU (1) | HUP0001674A3 (zh) |
| IL (1) | IL131256A (zh) |
| IS (1) | IS5160A (zh) |
| IT (1) | IT1289974B1 (zh) |
| NO (1) | NO994110L (zh) |
| NZ (1) | NZ337188A (zh) |
| PL (1) | PL188762B1 (zh) |
| PT (1) | PT1019362E (zh) |
| SK (1) | SK115399A3 (zh) |
| TR (1) | TR199902043T2 (zh) |
| WO (1) | WO1998038157A1 (zh) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1312018B1 (it) * | 1999-03-19 | 2002-04-04 | Fassi Aldo | Procedimento migliorato per la produzione di sali non igroscopicidella l(-)-carnitina. |
| KR100461572B1 (ko) * | 1999-03-27 | 2004-12-14 | 삼성정밀화학 주식회사 | Ｌ-카르니틴 칼슘 염과 이의 제조방법 |
| JP2003508488A (ja) * | 1999-09-03 | 2003-03-04 | シグマ−タウ・ヘルスサイエンス・ソシエタ・ペル・アチオニ | 超微細ｌ−カルニチン、その調製方法、それを含む組成物、及びその使用方法 |
| IT1316988B1 (it) * | 2000-02-10 | 2003-05-26 | Sigma Tau Ind Farmaceuti | Procedimento migliorato di preparazione industriale di mucati dellal-carnitina e di alcanoil l-carnitine. |
| IT1317013B1 (it) * | 2000-04-12 | 2003-05-26 | Biosalts Srl | Sostanze dolcificanti, particolarmente per il caffe' ed il the'. |
| ITRM20020055A1 (it) * | 2002-02-04 | 2003-08-04 | Aldo Fassi | Sali metallici di carnitine, integratori dietetici/nutritivi che li contengono e kit dietetici per contrastare disturbi sessuali in soggetti |
| US9084431B2 (en) * | 2005-07-05 | 2015-07-21 | Lonza Ltd. | Spray-Drying process for producing a dry caritine powder or granulate |
| US7523176B2 (en) * | 2005-08-02 | 2009-04-21 | International Business Machines Corporation | Method, apparatus, and computer program product for reconfiguring a storage area network to support the execution of an application automatically upon execution of the application |
| CA2637806A1 (en) * | 2005-11-07 | 2007-05-18 | Russell M. Jaffe | Compositions for regulating metabolic disorders and methods of use thereof |
| CN101209975B (zh) * | 2006-12-29 | 2010-12-01 | 沈阳科硕营养科技有限公司 | 左旋肉碱富马酸钙及其制备方法与用途 |
| JP2011068563A (ja) * | 2008-09-09 | 2011-04-07 | Mitsubishi Rayon Co Ltd | カルニチンフマル酸塩及びその製造方法 |
| KR101291186B1 (ko) * | 2010-07-23 | 2013-09-13 | 주식회사 셀트리온제약 | Ｌ-카르니틴 1,5-나프탈렌다이설폰산염 및 이를 포함하는 약제학적 조성물 |
| EP2425834A1 (en) * | 2010-09-06 | 2012-03-07 | Lonza Ltd. | Process for the production of l-carnitine tartrate |
| CN108383741A (zh) * | 2018-03-16 | 2018-08-10 | 开原亨泰化工有限公司 | 一种制备左旋肉碱成盐的新方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1230610A (en) * | 1983-11-02 | 1987-12-22 | Vincenzo Iannella | Process for the the preparation of l(-)carnitine hydrochloride and of l(-)carnitine inner salt |
| DE3463261D1 (en) * | 1983-12-28 | 1987-05-27 | Sigma Tau Ind Farmaceuti | Salts of l-carnitine and alkanoyl l-carnitines and process for preparing same |
| US5073376A (en) * | 1989-12-22 | 1991-12-17 | Lonza Ltd. | Preparations containing l-carnitine |
| DE4111913A1 (de) * | 1991-04-12 | 1992-10-15 | Degussa | Verfahren zur herstellung von l-carnitin aus d,l-carnitinnitrilsalzen |
| CH682485A5 (de) | 1991-08-13 | 1993-09-30 | Lonza Ag | Verfahren zur Herstellung optisch aktiver Carbonsäuren durch Racematspaltung. |
| TW397686B (en) * | 1993-08-11 | 2000-07-11 | Takeda Chemical Industries Ltd | Antacid compositions and pharmaceutical compositions |
| IT1272290B (it) * | 1994-06-20 | 1997-06-16 | Avantgarde Spa | Sale della l-carnitina e composizioni farmaceutiche che lo contengono per il trattamento di affezioni cutanee |
| IT1276225B1 (it) * | 1995-10-17 | 1997-10-27 | Sigma Tau Ind Farmaceuti | Composizioni farmaceutiche contenenti l-carnitina e alcanoil l- carnitine in associazione con resveratrolo o suoi derivati utili per |
| CN1177807C (zh) | 1996-05-31 | 2004-12-01 | 希格马托制药工业公司 | 稳定的、非吸湿性的l(-)肉碱和链烷酰基l(-)肉碱的盐和其制备方法以及含有此盐的固体口服组合物 |
-
1997
- 1997-02-25 IT IT97MI000409A patent/IT1289974B1/it active IP Right Grant
-
1998
- 1998-02-24 BR BR9807761A patent/BR9807761A/pt not_active IP Right Cessation
- 1998-02-24 JP JP53728998A patent/JP2001513096A/ja not_active Ceased
- 1998-02-24 WO PCT/EP1998/001039 patent/WO1998038157A1/en active IP Right Grant
- 1998-02-24 ES ES98913582T patent/ES2182290T3/es not_active Expired - Lifetime
- 1998-02-24 CA CA002281630A patent/CA2281630C/en not_active Expired - Fee Related
- 1998-02-24 EP EP98913582A patent/EP1019362B1/en not_active Expired - Lifetime
- 1998-02-24 HU HU0001674A patent/HUP0001674A3/hu unknown
- 1998-02-24 TR TR1999/02043T patent/TR199902043T2/xx unknown
- 1998-02-24 US US09/355,804 patent/US6271258B1/en not_active Expired - Fee Related
- 1998-02-24 CN CN98802829A patent/CN1248967A/zh active Pending
- 1998-02-24 CZ CZ19993028A patent/CZ290893B6/cs not_active IP Right Cessation
- 1998-02-24 DE DE69807245T patent/DE69807245T2/de not_active Expired - Fee Related
- 1998-02-24 EE EEP199900361A patent/EE03561B1/xx not_active IP Right Cessation
- 1998-02-24 AU AU68229/98A patent/AU724276B2/en not_active Ceased
- 1998-02-24 PT PT98913582T patent/PT1019362E/pt unknown
- 1998-02-24 SK SK1153-99A patent/SK115399A3/sk unknown
- 1998-02-24 PL PL98335350A patent/PL188762B1/pl not_active IP Right Cessation
- 1998-02-24 AT AT98913582T patent/ATE222233T1/de not_active IP Right Cessation
- 1998-02-24 DK DK98913582T patent/DK1019362T3/da active
- 1998-02-24 KR KR10-1999-7007778A patent/KR100538788B1/ko not_active IP Right Cessation
- 1998-02-24 NZ NZ337188A patent/NZ337188A/xx unknown
- 1998-02-24 IL IL13125698A patent/IL131256A/xx not_active IP Right Cessation
-
1999
- 1999-08-20 IS IS5160A patent/IS5160A/is unknown
- 1999-08-25 NO NO994110A patent/NO994110L/no not_active Application Discontinuation
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