1-(4-Fluorophenyl)-3-methylbutan-1-amine hydrochloride CAS 2285-93-0

Purity 97%+In StockPharmaceutical Standards
CAS No.2285-93-0
Molecular FormulaC11H16FN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluorophenyl)-3-methylbutan-1-amine hydrochloride CAS 2285-93-0 chemical structure

Description

Based on its molecular formula C11H16FNHCl, 1-(4-Fluorophenyl)-3-methylbutan-1-amine hydrochloride contains a nitrile group, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 217.71 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

1-(4-Fluorophenyl)-3-methylbutan-1-amine hydrochloride (CAS 2285-93-0) is a high-purity analytical reference standard with the molecular formula C11H16FNHCl and a molecular weight of 217.71 g/mol.

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 FormulaC11H16FN HCl
Molecular Weight217.71 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1957
Halogen ContentF/Cl-containing
Nitrogen Atoms1

Related Fluorophenyl Standards

Recommended Standards

Why CATO?