Raltegravir USP Impurity D and Raltegravir Oxalyl Analog Manufacturer in Mumbai
- Raltegravir USP Impurity D / Raltegravir Oxalyl Analog
- CAT No : ALL-RALT-8
- Chemical Name : 2-[(2-{4-[(4-Fluorobenzyl)carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl}propan-2-yl)amino]-2-oxoacetic acid
- Molecular Formula : C18H19FN4O6
- Molecular Weight : 406.37
- CAS Number : 1064706-98-4
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Raltegravir USP Impurity D / Raltegravir Oxalyl Analog, 2-[(2-{4-[(4-Fluorobenzyl)carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl}propan-2-yl)amino]-2-oxoacetic acid
- 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 Raltegravir USP Impurity D / Raltegravir Oxalyl Analog
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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