Cilastatin EP Impurity D CAS 141-79-7

Purity >90%In StockPharmacopoeial Impurity Standards
CAS No.141-79-7
Molecular FormulaC6H10O
Molecular Weight98.14 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Cilastatin EP Impurity D CAS 141-79-7 chemical structure

Description

The occurrence of Cilastatin EP Impurity D is closely related to a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Cilastatin EP Impurity D (CAS 141-79-7) is a certified pharmaceutical impurity reference standard with the molecular formula C6H10O and a molecular weight of 98.14 g/mol.

Cilastatin EP Impurity D (C6H10O) contains a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions.

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 Cilastatin EP Impurity D 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 FormulaC6H10O
Molecular Weight98.14 g/mol
Purity>90%
StorageStore at 2-8°C
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1957

Related Cilastatin Standards

Recommended Standards

Why CATO?