3-[2-Chloro-4-(tert-pentyl)phenoxy]pyrrolidinehydrochloride CAS 1220032-89-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1220032-89-2
Molecular FormulaC15H22ClNO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[2-Chloro-4-(tert-pentyl)phenoxy]pyrrolidinehydrochloride CAS 1220032-89-2 chemical structure

Description

CATO manufactures 3-[2-Chloro-4-(tert-pentyl)phenoxy]pyrrolidinehydrochloride 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.

CATO supplies 3-[2-Chloro-4-(tert-pentyl)phenoxy]pyrrolidinehydrochloride (CAS 1220032-89-2), a certified reference material (molecular formula C15H22ClNOHCl, MW 304.25 g/mol) for analytical method development and quality control.

The molecular framework of 3-[2-Chloro-4-(tert-pentyl)phenoxy]pyrrolidinehydrochloride (C15H22ClNOHCl) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H22ClNO HCl
Molecular Weight304.25 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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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