[4-(1,2,3,4-Tetrahydroisoquinolin-1-yl)phenyl]methanol CAS 199479-46-4

Purity 97%+In StockPharmaceutical Standards
CAS No.199479-46-4
Molecular FormulaC16H17NO
Molecular Weight239.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[4-(1,2,3,4-Tetrahydroisoquinolin-1-yl)phenyl]methanol CAS 199479-46-4 chemical structure

Description

The occurrence of [4-(1,2,3,4-Tetrahydroisoquinolin-1-yl)phenyl]methanol 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 [4-(1,2,3,4-Tetrahydroisoquinolin-1-yl)phenyl]methanol (CAS 199479-46-4), a certified reference material (molecular formula C16H17NO, MW 239.31 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, [4-(1,2,3,4-Tetrahydroisoquinolin-1-yl)phenyl]methanol is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 239.31 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC16H17NO
Molecular Weight239.31 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2013
Nitrogen Atoms1

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