2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one CAS 127876-36-2

Purity 97%+In StockPharmaceutical Standards
CAS No.127876-36-2
Molecular FormulaC14H11N3O
Molecular Weight237.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one CAS 127876-36-2 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one.

2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one (CAS 127876-36-2) is a high-purity analytical reference standard with the molecular formula C14H11N3O and a molecular weight of 237.26 g/mol.

2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one (C14H11N3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1-phenylethan-1-one 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 FormulaC14H11N3O
Molecular Weight237.26 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms3

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