Bacitracin EP Impurity G CAS 144572-54-3

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.144572-54-3
Molecular FormulaC6H10
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Bacitracin EP Impurity G CAS 144572-54-3 chemical structure

Description

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

CATO supplies Bacitracin EP Impurity G (CAS 144572-54-3), a pharmacopoeial impurity reference standard (molecular formula C6H10C4H8C2H6, MW 168.32 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Bacitracin EP Impurity G (C6H10C4H8C2H6) is characterized by an organic framework. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures Bacitracin EP Impurity G under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC6H10 C4H8 C2H6
Molecular Weight168.32 g/mol
Purity95%
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1998

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