1-methylpyrazolo[3,4-d]pyrimidin-4-amine CAS 5334-99-6

Purity 97%+In StockPharmaceutical Standards
CAS No.5334-99-6
Molecular FormulaC6H7N5
Molecular Weight149.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-methylpyrazolo[3,4-d]pyrimidin-4-amine CAS 5334-99-6 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 1-methylpyrazolo[3,4-d]pyrimidin-4-amine.

CATO supplies 1-methylpyrazolo[3,4-d]pyrimidin-4-amine (CAS 5334-99-6), a certified reference material (molecular formula C6H7N5, MW 149.15 g/mol) for analytical method development and quality control.

Owing to a nitrile group, an aromatic ring system, 1-methylpyrazolo[3,4-d]pyrimidin-4-amine is typically off-white to pale yellow liquid. Its solid-state physicochemical attributes — including a molecular weight of 149.15 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 1-methylpyrazolo[3,4-d]pyrimidin-4-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 FormulaC6H7N5
Molecular Weight149.15 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms5

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