Latamoxef Impurity 35 CAS CATO-C4X-179835

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-179835
Molecular FormulaC20H18O
Molecular Weight274.36 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Latamoxef Impurity 35 CAS CATO-C4X-179835 chemical structure

Description

Owing to a steroid core, a hydroxyl group, an ether linkage, Latamoxef Impurity 35 is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 274.36 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies Latamoxef Impurity 35 (CAS CATO-C4X-179835), a pharmacopoeial impurity reference standard (molecular formula C20H18O, MW 274.36 g/mol) used for the identification and quantification of trace impurities in APIs.

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 manufactures Latamoxef Impurity 35 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 FormulaC20H18O
Molecular Weight274.36 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present

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