3-(2-Methoxyphenyl)oxetan-3-amine hydrochloride CAS 1332765-89-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1332765-89-5
Molecular FormulaC10H13NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Methoxyphenyl)oxetan-3-amine hydrochloride CAS 1332765-89-5 chemical structure

Description

CATO manufactures 3-(2-Methoxyphenyl)oxetan-3-amine hydrochloride 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.

CATO supplies 3-(2-Methoxyphenyl)oxetan-3-amine hydrochloride (CAS 1332765-89-5), a certified reference material (molecular formula C10H13NO2HCl, MW 215.68 g/mol) for analytical method development and quality control.

Based on its molecular formula C10H13NO2HCl, 3-(2-Methoxyphenyl)oxetan-3-amine hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 215.68 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.

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

Physical & Chemical Properties

Molecular FormulaC10H13NO2 HCl
Molecular Weight215.68 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms1

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