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Velpatasvir Impurity 19

Picture of Velpatasvir Impurity 19
SZ CAT No SZ-V013036
CAS No NA
Mol.F. C45H50N8O4
Mol.Wt.  767.0
Inv. Status Custom Synthesis


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

Chemical Name: (S)-2-Amino-1-((2S,5S)-2-(9-(2-((2S,4S)-1-((R)-2-amino-2-phenylacetyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-methylbutan-1-one

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: COC[C@H]1C[C@@H](C2=NC=C(C3=CC4=C(C5=CC6=CC=C7C(NC([C@H]8N(C([C@@H](N)C(C)C)=O)[C@@H](C)CC8)=N7)=C6C=C5OC4)C=C3)N2)N(C([C@H](N)C9=CC=CC=C9)=O)C1

Velpatasvir Impurity 19 is chemically (S)-2-Amino-1-((2S,5S)-2-(9-(2-((2S,4S)-1-((R)-2-amino-2-phenylacetyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-methylbutan-1-one. Velpatasvir Impurity 19 is supplied with detailed characterization data compliant with regulatory guideline. Velpatasvir Impurity 19 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 Velpatasvir.

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.

UPLC Separation of forced degradation and process related impurities of Velpatasvir and structure elucidation by online LC-Quadrupole-Time of flight-Tandem mass Spectrometry
Md. Sattar Abdul*, Suneetha A.Research Journal of Pharmacy and Technology
Year : 2019, Volume : 12, Issue : 2
First page : ( 477) Last page : ( 482)

Stability indicating RP-HPLC Method development and Validation for the Estimation of Sofosbuvir, Velpatasvir and Voxilaprevir in Bulk and Pharmaceutical dosage form
Kokkirala, Tej Kumar; Suryakala, Duvvuri. Research Journal of Pharmacy and Technology; RaipurVol. 13, Iss. 11, (Nov 2020): 5063-5071. DOI:10.5958/0974-360X.2020.00887.2

RP-HPLC Method Development and Validation for Velpatasvir and Voxilaprevir by Simultaneous Determination in Bulk and Their Pharmaceutical Dosage Forms
DebasishSwainaAmrej SinghYadavaChandrasekharSasapuaVenkatakrishnaAkulabGananadhamuSamanthulaa
Microchemical JournalVolume 155, June 2020, 104657

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