n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine CAS 1158060-10-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1158060-10-6
Molecular FormulaC11H12Cl3N
Molecular Weight264.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine CAS 1158060-10-6 chemical structure

Description

The occurrence of n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine 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.

CATO supplies n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine (CAS 1158060-10-6), a certified reference material (molecular formula C11H12Cl3N, MW 264.58 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution, n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 264.58 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 n-(1-(2,3,4-Trichlorophenyl)ethyl)cyclopropanamine 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 FormulaC11H12Cl3N
Molecular Weight264.58 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.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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