N-(4-(1H-Imidazol-5-yl)phenyl)formamide CAS 89250-13-5

Purity 97%+In StockPharmaceutical Standards
CAS No.89250-13-5
Molecular FormulaC10H9N3O
Molecular Weight187.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-(1H-Imidazol-5-yl)phenyl)formamide CAS 89250-13-5 chemical structure

Description

The occurrence of N-(4-(1H-Imidazol-5-yl)phenyl)formamide is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

N-(4-(1H-Imidazol-5-yl)phenyl)formamide (CAS 89250-13-5) is a high-purity analytical reference standard with the molecular formula C10H9N3O and a molecular weight of 187.20 g/mol.

N-(4-(1H-Imidazol-5-yl)phenyl)formamide (C10H9N3O) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

CATO manufactures N-(4-(1H-Imidazol-5-yl)phenyl)formamide 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 FormulaC10H9N3O
Molecular Weight187.20 g/mol
AppearancePale yellow to yellow crystalline powder. (faint amine-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms3

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