N-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)benzimidamide CAS 132380-89-3

Purity 97%+In StockPharmaceutical Standards
CAS No.132380-89-3
Molecular FormulaC15H11ClN4O
Molecular Weight298.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)benzimidamide CAS 132380-89-3 chemical structure

Description

CATO manufactures N-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)benzimidamide 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.

CATO supplies N-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)benzimidamide (CAS 132380-89-3), a certified reference material (molecular formula C15H11ClN4O, MW 298.73 g/mol) for analytical method development and quality control.

N-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)benzimidamide (C15H11ClN4O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC15H11ClN4O
Molecular Weight298.73 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentCl-containing
Nitrogen Atoms4

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