Pravastatin EP Impurity D and Pravastatin BP Impurity D and Pravastatin Lactone Manufacturer in Mumbai
- Pravastatin EP Impurity D / Pravastatin BP Impurity D / Pravastatin Lactone
- CAT No : ALL-PRAV-12
- Chemical Name : (1S,3S,7S,8S,8aR)-3-Hydroxy-8-[2-[(2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (2S)-2-methylbutanoate
- Molecular Formula : C23H34O6
- Molecular Weight : 406.51
- CAS Number : 85956-22-5
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Pravastatin EP Impurity D / Pravastatin BP Impurity D / Pravastatin Lactone, (1S,3S,7S,8S,8aR)-3-Hydroxy-8-[2-[(2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (2S)-2-me
- Purity by HPLC : 95% +
Documents - COA, HNMR, 13CNMR, MASS, HPLC (by pharmacopoeia method with RT RRT results), IR and TGA will be provided with the purchase of Pravastatin EP Impurity D / Pravastatin BP Impurity D / Pravastatin Lactone
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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