Lopinavir EP Impurity O and Lopinavir O-Acyl Impurity (USP) Manufacturer in Mumbai
- Lopinavir EP Impurity O / Lopinavir O-Acyl Impurity (USP)
- CAT No : ALL-LOPI-16
- Chemical Name : (1S,3S)-1-[(1S)-1-[[2-(2,6-Dimethylphenoxy)acetyl]amino]-2-phenylethyl]-3-[[(2S)-3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanoyl]amino]-4phenylbutyl(2S)-3-methyl-2-[2-oxotetrahydropyrimidin1(2H)-yl]butanoate
- Molecular Formula : C46H62N6O7
- Molecular Weight : 811.02
- CAS Number : NA
- Solubility : Methanol, DMSO
- Storage : 2-8 °C
- Keywords : Lopinavir EP Impurity O / Lopinavir O-Acyl Impurity (USP), (1S,3S)-1-[(1S)-1-[[2-(2,6-Dimethylphenoxy)acetyl]amino]-2-phenylethyl]-3-[[(2S)-3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanoyl]amino]-4phenylbutyl(2S)-3-m
- 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 Lopinavir EP Impurity O / Lopinavir O-Acyl Impurity (USP)
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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