4-chloro-N,N-dimethyl-6-phenyl-1,3,5-triazin-2-amine CAS 36323-70-3

Purity 97%+In StockPharmaceutical Standards
CAS No.36323-70-3
Molecular FormulaC11H11ClN4
Molecular Weight234.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-chloro-N,N-dimethyl-6-phenyl-1,3,5-triazin-2-amine CAS 36323-70-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 234.68 g/mol gives 4-chloro-N,N-dimethyl-6-phenyl-1,3,5-triazin-2-amine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-chloro-N,N-dimethyl-6-phenyl-1,3,5-triazin-2-amine (CAS 36323-70-3) is a high-purity analytical reference standard with the molecular formula C11H11ClN4 and a molecular weight of 234.68 g/mol.

The molecular framework of 4-chloro-N,N-dimethyl-6-phenyl-1,3,5-triazin-2-amine (C11H11ClN4) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H11ClN4
Molecular Weight234.68 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1967
Halogen ContentCl-containing
Nitrogen Atoms4

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