1-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-amine CAS 618098-18-3

Purity 97%+In StockPharmaceutical Standards
CAS No.618098-18-3
Molecular FormulaC16H14FN3
Molecular Weight267.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-amine CAS 618098-18-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 267.30 g/mol gives 1-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-amine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-amine (CAS 618098-18-3) is a high-purity analytical reference standard with the molecular formula C16H14FN3 and a molecular weight of 267.30 g/mol.

1-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-amine (C16H14FN3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(4-Fluorophenyl)-3-(2-methylphenyl)-1h-pyrazol-5-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 FormulaC16H14FN3
Molecular Weight267.30 g/mol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing
Nitrogen Atoms3

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