5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole CAS 29334-69-8

Purity 97%+In StockPharmaceutical Standards
CAS No.29334-69-8
Molecular FormulaC16H13N3O2
Molecular Weight279.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole CAS 29334-69-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 279.29 g/mol gives 5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole (CAS 29334-69-8) is a high-purity analytical reference standard with the molecular formula C16H13N3O2 and a molecular weight of 279.29 g/mol.

The molecular framework of 5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole (C16H13N3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

As a certified reference material (CRM), 5-Methyl-1-(2-nitrophenyl)-3-phenyl-1H-pyrazole 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 FormulaC16H13N3O2
Molecular Weight279.29 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1965
Nitrogen Atoms3

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