Lovastatin EP Impurity B and Lovastatin Hydroxy Acid Sodium Salt and Mevinolinic Acid Sodium Salt Manufacturer in Mumbai
- Lovastatin EP Impurity B / Lovastatin Hydroxy Acid Sodium Salt / Mevinolinic Acid Sodium Salt
- CAT No : ALL-LOV-4
- Chemical Name : (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[[(2S)-2-methylbutanoyl]oxy]-1,2,6,7, 8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid sodium salt
- Molecular Formula : C24H37NaO6
- Molecular Weight : 444.54
- CAS Number : 75225-50-2
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Lovastatin EP Impurity B / Lovastatin Hydroxy Acid Sodium Salt / Mevinolinic Acid Sodium Salt, (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[[(2S)-2-methylbutanoyl]oxy]-1,2,6,7, 8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyh
- 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 B / Lovastatin Hydroxy Acid Sodium Salt / Mevinolinic Acid Sodium Salt
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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