Raltegravir Impurity 10

N° de SZ CAT:	SZ-R009029
Número CAS	NA
Mol.F.	C8H12N4O3
Peso Molecular	212.2
Status de Fatura	Custom Synthesis

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Nome Químico: N-(1-Amino-2-methyl-1-oxopropan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C(C1=NN=C(C)O1)NC(C)(C)C(N)=O

Development and validation of stability indicating RP-HPLC assay method of raltegravir in tablet dosage forms
By Shirisha, V.; Sairaju, B.; Illendula, Santhosh; Dutt, K. Rajeswar
From World Journal of Pharmacy and Pharmaceutical Sciences (2019), 8(10), 668-692

Stability indicating reverse-phase high performance liquid chromatography method for the determination of raltegravir in bulk and pharmaceutical formulation
By Annapurna, Mukthinuthalapati Mathrusri; Teja, Gunnam Ravi; Hemchand, S.; Babu, R. Ravi Chandra
From International Journal of Green Pharmacy (2018), 12(1Suppl.), S177-S180

Development and validation of RP-HPLC method for determination of raltegravir and its impurities in bulk drug and dosage forms
By Balaji, M.; AppaRao, K. M. Ch.; Ramakrishna, K.; Srinivasarao, V.
From Pharma Science Monitor (2014), 5(3Suppl.1), 187-196, 10 pp.

Raltegravir Impurity 10 is chemically N-(1-Amino-2-methyl-1-oxopropan-2-yl)-5-methyl-1,3,4-oxadiazole-2-carboxamide. Raltegravir Impurity 10 is supplied with detailed characterization data compliant with regulatory guideline. Raltegravir Impurity 10 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Raltegravir.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Raltegravir Impurity 10

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