Abrocitinib Impurity 16 DiHBr CAS 1622903-42-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1622903-42-7
Molecular FormulaC18H21N5O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Abrocitinib Impurity 16 DiHBr CAS 1622903-42-7 chemical structure

Description

The occurrence of Abrocitinib Impurity 16 DiHBr is closely related to a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Abrocitinib Impurity 16 DiHBr (CAS 1622903-42-7), a certified reference material (molecular formula C18H21N5O2SHBr, MW 452.37 g/mol) for analytical method development and quality control.

The molecular framework of Abrocitinib Impurity 16 DiHBr (C18H21N5O2SHBr) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures Abrocitinib Impurity 16 DiHBr 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 FormulaC18H21N5O2S 2*HBr
Molecular Weight452.37 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentBr-containing
Nitrogen Atoms5
Sulfur Atoms1

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