2-(tert-Butyl)phenyl 3-pyrrolidinylmethyl etherhydrochloride CAS 1146960-38-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1146960-38-4
Molecular FormulaC15H23NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)phenyl 3-pyrrolidinylmethyl etherhydrochloride CAS 1146960-38-4 chemical structure

Description

The molecular framework of 2-(tert-Butyl)phenyl 3-pyrrolidinylmethyl etherhydrochloride (C15H23NOHCl) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2-(tert-Butyl)phenyl 3-pyrrolidinylmethyl etherhydrochloride (CAS 1146960-38-4), molecular formula C15H23NOHCl and molecular weight 269.81 g/mol, is a CATO reference standard with documented purity and traceability.

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

As a certified reference material (CRM), 2-(tert-Butyl)phenyl 3-pyrrolidinylmethyl etherhydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC15H23NO HCl
Molecular Weight269.81 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.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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