(E)-4-((4-Aminophenyl)Diazenyl)-2-chlorophenol CAS 669092-47-1

Purity 97%+In StockPharmaceutical Standards
CAS No.669092-47-1
Molecular FormulaC12H10ClN3O
Molecular Weight247.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-4-((4-Aminophenyl)Diazenyl)-2-chlorophenol CAS 669092-47-1 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 (E)-4-((4-Aminophenyl)Diazenyl)-2-chlorophenol.

CATO supplies (E)-4-((4-Aminophenyl)Diazenyl)-2-chlorophenol (CAS 669092-47-1), a certified reference material (molecular formula C12H10ClN3O, MW 247.68 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, (E)-4-((4-Aminophenyl)Diazenyl)-2-chlorophenol is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 247.68 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC12H10ClN3O
Molecular Weight247.68 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms3

Related E Standards

Recommended Standards

Why CATO?