2-Chloro-4-methylphenyl 3-pyrrolidinylmethyl-ether hydrochloride CAS 1219956-91-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1219956-91-8
Molecular FormulaC12H16ClNO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-4-methylphenyl 3-pyrrolidinylmethyl-ether hydrochloride CAS 1219956-91-8 chemical structure

Description

The molecular framework of 2-Chloro-4-methylphenyl 3-pyrrolidinylmethyl-ether hydrochloride (C12H16ClNOHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 2-Chloro-4-methylphenyl 3-pyrrolidinylmethyl-ether hydrochloride (CAS 1219956-91-8), a certified reference material (molecular formula C12H16ClNOHCl, MW 262.17 g/mol) for analytical method development and quality control.

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 2-Chloro-4-methylphenyl 3-pyrrolidinylmethyl-ether hydrochloride 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 FormulaC12H16ClNO HCl
Molecular Weight262.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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