[(1R,2S)-1-methyl-2-phenylcyclopropyl]methanamine hydrochloride CAS 1808843-59-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1808843-59-5
Molecular FormulaC11H15N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[(1R,2S)-1-methyl-2-phenylcyclopropyl]methanamine hydrochloride CAS 1808843-59-5 chemical structure

Description

CATO supplies [(1R,2S)-1-methyl-2-phenylcyclopropyl]methanamine hydrochloride (CAS 1808843-59-5), a certified reference material (molecular formula C11H15NHCl, MW 197.71 g/mol) for analytical method development and quality control.

[(1R,2S)-1-methyl-2-phenylcyclopropyl]methanamine hydrochloride (C11H15NHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 manufactures [(1R,2S)-1-methyl-2-phenylcyclopropyl]methanamine 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 FormulaC11H15N HCl
Molecular Weight197.71 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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