Metoclopramide EP Impurity E CAS 100-36-7

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.100-36-7
Molecular FormulaC6H16N2
Molecular Weight116.20 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Metoclopramide EP Impurity E CAS 100-36-7 chemical structure

Description

CATO manufactures Metoclopramide EP Impurity E 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.

CATO supplies Metoclopramide EP Impurity E (CAS 100-36-7), a pharmacopoeial impurity reference standard (molecular formula C6H16N2, MW 116.20 g/mol) used for the identification and quantification of trace impurities in APIs.

Owing to an organic framework, Metoclopramide EP Impurity E is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 116.20 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC6H16N2
Molecular Weight116.20 g/mol
Purity>95%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)0.0
CAS Registry Year (est.)1957
Nitrogen Atoms2

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