8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-2-phenylbutanoate hydrochloride CAS 1233641-91-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1233641-91-2
Molecular FormulaC18H25NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-2-phenylbutanoate hydrochloride CAS 1233641-91-2 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO supplies 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-2-phenylbutanoate hydrochloride (CAS 1233641-91-2), a certified reference material (molecular formula C18H25NO2HCl, MW 323.86 g/mol) for analytical method development and quality control.

Based on its molecular formula C18H25NO2HCl, 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-2-phenylbutanoate hydrochloride contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 323.86 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl-2-phenylbutanoate 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 FormulaC18H25NO2 HCl
Molecular Weight323.86 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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