Pravastatin EP Impurity G and Pravastatin BP Impurity G and Pravastatin Oxidation Impurity (USP) and Pravastatin Dihydronaphthalene Acid Impurity (Sodium Salt) Manufacturer in Mumbai
- Pravastatin EP Impurity G / Pravastatin BP Impurity G / Pravastatin Oxidation Impurity (USP) / Pravastatin Dihydronaphthalene Acid Impurity (Sodium Salt)
- CAT No : ALL-PRAV-15
- Chemical Name : (?R,?R,1S,2S)-1,2-Dihydro-?,?,6-trihydroxy-2-methyl-1-naphthaleneheptanoic acid sodium salt
- Molecular Formula : C18H23NaO5
- Molecular Weight : 342.36
- CAS Number : 720666-74-0 & 136590-28-8 (Sodium Salt) ; 136590-28-8 (Acid)
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Pravastatin EP Impurity G / Pravastatin BP Impurity G / Pravastatin Oxidation Impurity (USP) / Pravastatin Dihydronaphthalene Acid Impurity (Sodium Salt), (?R,?R,1S,2S)-1,2-Dihydro-?,?,6-trihydroxy-2-methyl-1-naphthalenehe
- 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 G / Pravastatin BP Impurity G / Pravastatin Oxidation Impurity (USP) / Pravastatin Dihydronaphthalene Acid Impurity (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.
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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