1-Benzyl-5-iodo-4-phenyl-1H-1,2,3-triazole CAS 860002-66-0

Purity 97%+In StockPharmaceutical Standards
CAS No.860002-66-0
Molecular FormulaC15H12IN3
Molecular Weight361.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Benzyl-5-iodo-4-phenyl-1H-1,2,3-triazole CAS 860002-66-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 361.18 g/mol gives 1-Benzyl-5-iodo-4-phenyl-1H-1,2,3-triazole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-Benzyl-5-iodo-4-phenyl-1H-1,2,3-triazole (CAS 860002-66-0) is a high-purity analytical reference standard with the molecular formula C15H12IN3 and a molecular weight of 361.18 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine substitution, 1-Benzyl-5-iodo-4-phenyl-1H-1,2,3-triazole is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 361.18 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-Benzyl-5-iodo-4-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 FormulaC15H12IN3
Molecular Weight361.18 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1987
Halogen ContentI-containing
Nitrogen Atoms3

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