N-(4-isopropylbenzyl)cyclopropanamine hydrochloride CAS 1049681-03-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1049681-03-9
Molecular FormulaC13H19N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-isopropylbenzyl)cyclopropanamine hydrochloride CAS 1049681-03-9 chemical structure

Description

The occurrence of N-(4-isopropylbenzyl)cyclopropanamine hydrochloride is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

N-(4-isopropylbenzyl)cyclopropanamine hydrochloride (CAS 1049681-03-9), molecular formula C13H19NHCl and molecular weight 225.76 g/mol, is a CATO reference standard with documented purity and traceability.

N-(4-isopropylbenzyl)cyclopropanamine hydrochloride (C13H19NHCl) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

As a certified reference material (CRM), N-(4-isopropylbenzyl)cyclopropanamine hydrochloride 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 FormulaC13H19N HCl
Molecular Weight225.76 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

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