4-(Pentyloxy)-N-{1-[4-(pentyloxy)benzoyl]-1H-1,3-benzodiazol-5-yl}benzamide CAS 865660-33-9

Purity 97%+In StockPharmaceutical Standards
CAS No.865660-33-9
Molecular FormulaC31H35N3O4
Molecular Weight513.63 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Pentyloxy)-N-{1-[4-(pentyloxy)benzoyl]-1H-1,3-benzodiazol-5-yl}benzamide CAS 865660-33-9 chemical structure

Description

CATO manufactures 4-(Pentyloxy)-N-{1-[4-(pentyloxy)benzoyl]-1H-1,3-benzodiazol-5-yl}benzamide 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.

4-(Pentyloxy)-N-{1-[4-(pentyloxy)benzoyl]-1H-1,3-benzodiazol-5-yl}benzamide (CAS 865660-33-9) is a high-purity analytical reference standard with the molecular formula C31H35N3O4 and a molecular weight of 513.63 g/mol.

4-(Pentyloxy)-N-{1-[4-(pentyloxy)benzoyl]-1H-1,3-benzodiazol-5-yl}benzamide (C31H35N3O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC31H35N3O4
Molecular Weight513.63 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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