(+)-Bicifadine Hydrochloride (1R,5S)-1-(4-Methylphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride 66504-82-3 CAS 66504-82-3

Purity 97%+In StockPharmaceutical Standards
CAS No.66504-82-3
Molecular FormulaC12H15N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(+)-Bicifadine Hydrochloride
(1R,5S)-1-(4-Methylphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride
66504-82-3 CAS 66504-82-3 chemical structure

Description

The molecular framework of (+)-Bicifadine Hydrochloride (1R,5S)-1-(4-Methylphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride 66504-82-3 (C12H15NHCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, 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).

(+)-Bicifadine Hydrochloride (1R,5S)-1-(4-Methylphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride 66504-82-3 (CAS 66504-82-3) is a high-purity analytical reference standard with the molecular formula C12H15NHCl and a molecular weight of 209.72 g/mol.

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 (+)-Bicifadine Hydrochloride (1R,5S)-1-(4-Methylphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride 66504-82-3 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 FormulaC12H15N HCl
Molecular Weight209.72 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentCl-containing
Nitrogen Atoms1

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