5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine CAS 1355175-66-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1355175-66-4
Molecular FormulaC15H19N3
Molecular Weight241.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine CAS 1355175-66-4 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 5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine.

5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine (CAS 1355175-66-4) is a high-purity analytical reference standard with the molecular formula C15H19N3 and a molecular weight of 241.33 g/mol.

Based on its molecular formula C15H19N3, 5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 241.33 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.

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 5-(1-Aminoethyl)-N,4-dimethyl-N-phenylpyridin-2-amine 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 FormulaC15H19N3
Molecular Weight241.33 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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