4,5-Bis(chloromethyl)-1-phenyl-1H-1,2,3-triazole CAS 104503-32-4

Purity 97%+In StockPharmaceutical Standards
CAS No.104503-32-4
Molecular FormulaC10H9Cl2N3
Molecular Weight242.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,5-Bis(chloromethyl)-1-phenyl-1H-1,2,3-triazole CAS 104503-32-4 chemical structure

Description

Based on its molecular formula C10H9Cl2N3, 4,5-Bis(chloromethyl)-1-phenyl-1H-1,2,3-triazole 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 242.10 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 4,5-Bis(chloromethyl)-1-phenyl-1H-1,2,3-triazole (CAS 104503-32-4), a certified reference material (molecular formula C10H9Cl2N3, MW 242.10 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.

CATO manufactures 4,5-Bis(chloromethyl)-1-phenyl-1H-1,2,3-triazole 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 FormulaC10H9Cl2N3
Molecular Weight242.10 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.)1986
Halogen ContentCl-containing
Nitrogen Atoms3

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