3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile CAS 876299-39-7

Purity 97%+In StockPharmaceutical Standards
CAS No.876299-39-7
Molecular FormulaC14H16N4
Molecular Weight240.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile CAS 876299-39-7 chemical structure

Description

The occurrence of 3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile (CAS 876299-39-7) is a high-purity analytical reference standard with the molecular formula C14H16N4 and a molecular weight of 240.30 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 240.30 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.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 3-(5-Amino-3-(tert-butyl)-1H-pyrazol-1-yl)benzonitrile 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 FormulaC14H16N4
Molecular Weight240.30 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms4

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