1-(4-Bromophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine CAS 99867-27-3

Purity 97%+In StockPharmaceutical Standards
CAS No.99867-27-3
Molecular FormulaC11H8BrN5
Molecular Weight290.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Bromophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine CAS 99867-27-3 chemical structure

Description

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 supplies 1-(4-Bromophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (CAS 99867-27-3), a certified reference material (molecular formula C11H8BrN5, MW 290.12 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine substitution, 1-(4-Bromophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 290.12 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 1-(4-Bromophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H8BrN5
Molecular Weight290.12 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentBr-containing
Nitrogen Atoms5

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