N-(1-(pyridin-4-yl)ethyl)cyclohexanamine CAS 1019594-24-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1019594-24-1
Molecular FormulaC13H20N2
Molecular Weight204.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(1-(pyridin-4-yl)ethyl)cyclohexanamine CAS 1019594-24-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(1-(pyridin-4-yl)ethyl)cyclohexanamine.

N-(1-(pyridin-4-yl)ethyl)cyclohexanamine (CAS 1019594-24-1), molecular formula C13H20N2 and molecular weight 204.31 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C13H20N2, N-(1-(pyridin-4-yl)ethyl)cyclohexanamine contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 204.31 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 N-(1-(pyridin-4-yl)ethyl)cyclohexanamine 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 FormulaC13H20N2
Molecular Weight204.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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