Oseltamivir EP Impurity G (HCl Salt) and Oseltamivir BP Impurity G Manufacturer in Mumbai
- Oseltamivir EP Impurity G (HCl Salt) / Oseltamivir BP Impurity G
- CAT No : ALL-OSE-7
- Chemical Name : 4-N-Desacetyl-5-N-Acetyl Oseltamivir HCl;Ethyl (3R,4R,5S)-5-acetamido-4-amino-3-(1-ethylpropoxy)cyclohex-1-ene-1-carboxylate HCl
- Molecular Formula : C16H28N2O4 (base);C16H29ClN2O4 (HCl Salt)
- Molecular Weight : 312.4;348.87
- CAS Number : 956267-10-0 (base)
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Oseltamivir EP Impurity G (HCl Salt) / Oseltamivir BP Impurity G, 4-N-Desacetyl-5-N-Acetyl Oseltamivir HCl;Ethyl (3R,4R,5S)-5-acetamido-4-amino-3-(1-ethylpropoxy)cyclohex-1-ene-1-carboxylate HCl
- Purity by HPLC : 95% +
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COADocuments - COA, HNMR, 13CNMR, MASS, HPLC (by pharmacopoeia method with RT RRT results), IR and TGA will be provided with the purchase of Oseltamivir EP Impurity G (HCl Salt) / Oseltamivir BP Impurity G
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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