Lovastatin EP Impurity F and Tiglistatin and 2',3'-Didehydro Lovastati Manufacturer in Mumbai
- Lovastatin EP Impurity F / Tiglistatin / 2',3'-Didehydro Lovastati
- CAT No : ALL-LOV-8
- Chemical Name : (1S,3R,7S,8S,8aR)-8-[2-[(2R,4R)-4-Hydroxy-6-oxotetrahydro-2H-pyran-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8ahexahydronaphthalen-1-yl (2Z)-2-methylbut-2-enoate
- Molecular Formula : C24H34O5
- Molecular Weight : 402.52
- CAS Number : NA
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Lovastatin EP Impurity F / Tiglistatin / 2',3'-Didehydro Lovastati, (1S,3R,7S,8S,8aR)-8-[2-[(2R,4R)-4-Hydroxy-6-oxotetrahydro-2H-pyran-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8ahexahydronaphthalen-1-yl (2Z)-2-methylbut-2-enoate
- Purity by HPLC : 95% +
COADocuments - COA, HNMR, 13CNMR, MASS, HPLC (by pharmacopoeia method with RT RRT results), IR and TGA will be provided with the purchase of Lovastatin EP Impurity F / Tiglistatin / 2',3'-Didehydro Lovastati
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Allmpus laboratories private limited (Based in India) are in Business for science & innovation, it is continuously involved in design, research , development with cost effective synthesis and finding out new techniques of isolation & purification.
For Business Queries
ashish@allmpus.comFor Career Related Queries
girish@allmpus.comOur Locations
Corporate Office
Mumbai Maharashtra, India
R&D Centers
Amravati, Maharashtra, India
Manufacturing Plant
Amravati, Maharashtra, India
Services
- Contract Research
- Synthesis of API related Compound, Process Impurity, Metabolite and are acceptable to all regulatory agencies & also used for ANDA filing /DMF filing and genotoxic study.
- Synthesis of NCE’S
- Synthesis of Medicinal library
- Synthesis of Molecules for SAR studies
- Synthesis of references compound and scale up to kg scale.
- Analytical Support