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Raltegravir EP Impurity D

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SZ目录编号:	SZ-R009004
CAS 号	1064706-98-4
分子式	C18H19FN4O6
分子量	406.4
投资状态	In Stock

Product Overview Description Technical Data

化学名称: [[2-[4-[[(4-fluorophenyl)methyl]carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl]propan-2-yl]amino]oxoacetic acid (as per EP)

异名: Raltegravir Oxalyl Analog

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: O=C(O)C(NC(C)(C1=NC(C(NCC2=CC=C(F)C=C2)=O)=C(O)C(N1C)=O)C)=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.

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Raltegravir EP Impurity D

SZ目录编号:	SZ-R009004
CAS 号	1064706-98-4
分子式	C18H19FN4O6
分子量	406.4
投资状态	In Stock

Disclaimer

SynZeal will update these details as per new development or finding in product specification without further noticed.

化学名称: [[2-[4-[[(4-fluorophenyl)methyl]carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl]propan-2-yl]amino]oxoacetic acid (as per EP)

异名: Raltegravir Oxalyl Analog

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: O=C(O)C(NC(C)(C1=NC(C(NCC2=CC=C(F)C=C2)=O)=C(O)C(N1C)=O)C)=O

Raltegravir EP Impurity D is chemically [[2-[4-[[(4-fluorophenyl)methyl]carbamoyl]-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl]propan-2-yl]amino]oxoacetic acid (as per EP) . It is also known as Raltegravir Oxalyl Analog. Raltegravir EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Raltegravir EP Impurity D 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.