Etodolac EP Impurity I

SZ CAT No:	SZ-E023010
CAS No	NA
Mol.F.	C27H32N2O3
Mol.Wt.	432.6
Inv. Status	In Stock

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Chemical Name: (3RS)-3-[7-ethyl-3-(2-hydroxyethyl)-1H-indol-2-yl]-3-(7-ethyl-1H-indol-3-yl)pentanoic acid (as per EP)

Synonym: Etodolac Dimer

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: CCC(C1=CNC2=C1C=CC=C2CC)(C(N3)=C(CCO)C4=C3C(CC)=CC=C4)CC(O)=O

Method development and validation of HPLC for simultaneous determination of etodolac
By Srinivasarao, Kandimalla; Pai, K. Vasantha Kumar
From Pharma Chemica (2015), 7(3), 284-288

Improvement of the etodolac purity test by reversed phase high-performance liquid chromatography
By Ammar, A.; Surmann, P.
From Pharmazie (2008), 63(12), 913-914

Determination of enantiomeric impurity of etodolac by capillary electrophoresis using (2-hydroxypropyl)-β-cyclodextrin
By Dung, Phan Thanh; Ko, Mi Young; Choi, Hyun Ju; Sin, Kwan Seog; Kim, Kyeong Ho
From Archives of Pharmacal Research (2008), 31(9), 1218-1223

Etodolac EP Impurity I is chemically (3RS)-3-[7-ethyl-3-(2-hydroxyethyl)-1H-indol-2-yl]-3-(7-ethyl-1H-indol-3-yl)pentanoic acid (as per EP). It is also known as Etodolac Dimer. Etodolac EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Etodolac EP Impurity I 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 Etodolac.

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.

Etodolac EP Impurity I

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