1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile CAS 1049772-79-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1049772-79-3
Molecular FormulaC6H4F3N3
Molecular Weight175.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile CAS 1049772-79-3 chemical structure

Description

Owing to a nitrile group, fluorine substitution, an aromatic ring system, 1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 175.11 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.

1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile (CAS 1049772-79-3) is a high-purity analytical reference standard with the molecular formula C6H4F3N3 and a molecular weight of 175.11 g/mol.

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

CATO manufactures 1-Methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrile 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 FormulaC6H4F3N3
Molecular Weight175.11 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms3

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