N-[4-(Methylthio)benzyl]cyclopropanamine hydrochloride CAS 1049696-51-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1049696-51-6
Molecular FormulaC11H15NS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-[4-(Methylthio)benzyl]cyclopropanamine hydrochloride CAS 1049696-51-6 chemical structure

Description

N-[4-(Methylthio)benzyl]cyclopropanamine hydrochloride (C11H15NSHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

N-[4-(Methylthio)benzyl]cyclopropanamine hydrochloride (CAS 1049696-51-6), molecular formula C11H15NSHCl and molecular weight 229.77 g/mol, is a CATO reference standard with documented purity and traceability.

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 N-[4-(Methylthio)benzyl]cyclopropanamine 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 FormulaC11H15NS HCl
Molecular Weight229.77 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.)1988
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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