5-Methyl-N-(pyridin-4-yl)-3-(p-tolyl)pyrazolo[1,5-a]pyrimidin-7-amine CAS 902035-75-0

Purity 97%+In StockPharmaceutical Standards
CAS No.902035-75-0
Molecular FormulaC19H17N5
Molecular Weight315.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Methyl-N-(pyridin-4-yl)-3-(p-tolyl)pyrazolo[1,5-a]pyrimidin-7-amine CAS 902035-75-0 chemical structure

Description

CATO manufactures 5-Methyl-N-(pyridin-4-yl)-3-(p-tolyl)pyrazolo[1,5-a]pyrimidin-7-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.

CATO supplies 5-Methyl-N-(pyridin-4-yl)-3-(p-tolyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS 902035-75-0), a certified reference material (molecular formula C19H17N5, MW 315.37 g/mol) for analytical method development and quality control.

The molecular framework of 5-Methyl-N-(pyridin-4-yl)-3-(p-tolyl)pyrazolo[1,5-a]pyrimidin-7-amine (C19H17N5) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 FormulaC19H17N5
Molecular Weight315.37 g/mol
AppearancePale yellow to yellow crystalline powder
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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms5

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