Bupropion Impurity 35

N° de SZ CAT:	SZ-B001089
Número CAS	1005002-74-3
Mol.F.	C11H11ClO3
Peso Molecular	226.7
Status de Fatura

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

Nome Químico: 1-(3-Chlorophenyl)-2-oxopropyl acetate

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC(OC(C1=CC=CC(Cl)=C1)C(C)=O)=O

Method development and validation of a novel anti-depressant bupropion by RP-HPLC
By Kumar, Anil; Agrawal, Dilip; Bansal, Mukesh
From Asian Journal of Pharmaceutical Research and Development (2020), 8(3), 211-223

MSn, LC-MS-TOF and LC-PDA studies for identification of new degradation impurities of bupropion
By Bansal, Rohit; Saini, Balraj; Bansal, Yogita; Bansal, Gulshan
From Biomedical Chromatography (2013), 27(11), 1387-1397

Impurities in bupropion hydrochloride sustained-release tablets
By Cheng, Shu-qiao; Cai, Mei; Chen, Min-hui; Wang, Yu
From Zhongnan Yaoxue (2013), 11(2), 89-92

Bupropion Impurity 35 is chemically 1-(3-Chlorophenyl)-2-oxopropyl acetate. Bupropion Impurity 35 is supplied with detailed characterization data compliant with regulatory guideline. Bupropion Impurity 35 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 Bupropion.

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.

Bupropion Impurity 35

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