3-(((3-Methylbutan-2-yl)amino)methyl)phenol CAS 960250-51-5

Purity 97%+In StockPharmaceutical Standards
CAS No.960250-51-5
Molecular FormulaC12H19NO
Molecular Weight193.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(((3-Methylbutan-2-yl)amino)methyl)phenol CAS 960250-51-5 chemical structure

Description

The occurrence of 3-(((3-Methylbutan-2-yl)amino)methyl)phenol is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(((3-Methylbutan-2-yl)amino)methyl)phenol (CAS 960250-51-5), a certified reference material (molecular formula C12H19NO, MW 193.29 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H19NO, 3-(((3-Methylbutan-2-yl)amino)methyl)phenol contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 193.29 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.

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 FormulaC12H19NO
Molecular Weight193.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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