1-[(4-tert-Butylphenyl)methyl]-N-ethyl-1H-1,3-benzodiazol-2-amine CAS 866131-99-9

Purity 97%+In StockPharmaceutical Standards
CAS No.866131-99-9
Molecular FormulaC20H25N3
Molecular Weight307.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[(4-tert-Butylphenyl)methyl]-N-ethyl-1H-1,3-benzodiazol-2-amine CAS 866131-99-9 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-tert-Butylphenyl)methyl]-N-ethyl-1H-1,3-benzodiazol-2-amine.

1-[(4-tert-Butylphenyl)methyl]-N-ethyl-1H-1,3-benzodiazol-2-amine (CAS 866131-99-9), molecular formula C20H25N3 and molecular weight 307.43 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 1-[(4-tert-Butylphenyl)methyl]-N-ethyl-1H-1,3-benzodiazol-2-amine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 307.43 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.

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 FormulaC20H25N3
Molecular Weight307.43 g/mol
AppearancePale yellow to yellow crystalline powder
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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