Nizatidine Impurity 12 CAS 534-07-6

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.534-07-6
Molecular FormulaC3H4Cl2O
Molecular Weight126.97 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Nizatidine Impurity 12 CAS 534-07-6 chemical structure

Description

Owing to a hydroxyl group, an ether linkage, chlorine substitution, Nizatidine Impurity 12 is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 126.97 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies Nizatidine Impurity 12 (CAS 534-07-6), a pharmacopoeial impurity reference standard (molecular formula C3H4Cl2O, MW 126.97 g/mol) used for the identification and quantification of trace impurities in APIs.

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

CATO manufactures Nizatidine Impurity 12 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 FormulaC3H4Cl2O
Molecular Weight126.97 g/mol
Purity>95%
StorageStore at 2-8°C, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1957
Halogen ContentCl-containing

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