1-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine CAS 83783-69-1

Purity 97%+In StockPharmaceutical Standards
CAS No.83783-69-1
Molecular FormulaC14H12FN3
Molecular Weight241.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine CAS 83783-69-1 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 1-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine.

CATO supplies 1-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine (CAS 83783-69-1), a certified reference material (molecular formula C14H12FN3, MW 241.26 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution, 1-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 241.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

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-(4-Fluorobenzyl)-1H-benzo[d]imidazol-2-amine 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 FormulaC14H12FN3
Molecular Weight241.26 g/mol
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980
Halogen ContentF-containing
Nitrogen Atoms3

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