Ruxolitinib Impurity 232 CAS CATO-C4X-2058232

Purity ≥95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-2058232
Molecular FormulaC7H13ClO2
Molecular Weight164.63 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ruxolitinib Impurity 232 CAS CATO-C4X-2058232 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.

Ruxolitinib Impurity 232 (CAS CATO-C4X-2058232) is a certified pharmaceutical impurity reference standard with the molecular formula C7H13ClO2 and a molecular weight of 164.63 g/mol.

Structurally, Ruxolitinib Impurity 232 (C7H13ClO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 1.0, corresponding to approximately 1 ring(s) or double-bond equivalent(s). With a molecular weight of 164.63 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures Ruxolitinib Impurity 232 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 FormulaC7H13ClO2
Molecular Weight164.63 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)
StabilityContains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)1.0
Halogen ContentCl-containing

Related Ruxolitinib Standards

Recommended Standards

Why CATO?