Baricitinib Impurity 43 CAS 1401222-91-0

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.1401222-91-0
Molecular FormulaC5H9NO3S
Molecular Weight163.19 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Baricitinib Impurity 43 CAS 1401222-91-0 chemical structure

Description

As a process- or degradation-related impurity, Baricitinib Impurity 43 (CAS 1401222-91-0, C5H9NO3S) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Owing to an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, Baricitinib Impurity 43 is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 163.19 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.

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 Baricitinib Impurity 43 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 FormulaC5H9NO3S
Molecular Weight163.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityLight-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1991
Nitrogen Atoms1
Sulfur Atoms1

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