3-(2,3,4-Trichlorophenyl)-1H-pyrazol-5-amine CAS 502133-06-4

Purity 97%+In StockPharmaceutical Standards
CAS No.502133-06-4
Molecular FormulaC9H6Cl3N3
Molecular Weight262.52 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2,3,4-Trichlorophenyl)-1H-pyrazol-5-amine CAS 502133-06-4 chemical structure

Description

Based on its molecular formula C9H6Cl3N3, 3-(2,3,4-Trichlorophenyl)-1H-pyrazol-5-amine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 262.52 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 3-(2,3,4-Trichlorophenyl)-1H-pyrazol-5-amine (CAS 502133-06-4), a certified reference material (molecular formula C9H6Cl3N3, MW 262.52 g/mol) for analytical method development and quality control.

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-(2,3,4-Trichlorophenyl)-1H-pyrazol-5-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 FormulaC9H6Cl3N3
Molecular Weight262.52 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentCl-containing
Nitrogen Atoms3

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