1-(5-Phenylpyrimidin-2-yl)methanamine hydrochloride CAS 1240603-02-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1240603-02-4
Molecular FormulaC11H11N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(5-Phenylpyrimidin-2-yl)methanamine hydrochloride CAS 1240603-02-4 chemical structure

Description

CATO manufactures 1-(5-Phenylpyrimidin-2-yl)methanamine hydrochloride 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.

1-(5-Phenylpyrimidin-2-yl)methanamine hydrochloride (CAS 1240603-02-4), molecular formula C11H11N3HCl and molecular weight 221.69 g/mol, is a CATO reference standard with documented purity and traceability.

1-(5-Phenylpyrimidin-2-yl)methanamine hydrochloride (C11H11N3HCl) 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC11H11N3 HCl
Molecular Weight221.69 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms3

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