3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline CAS 5423-67-6

Purity 97%+In StockPharmaceutical Standards
CAS No.5423-67-6
Molecular FormulaC13H13NO
Molecular Weight199.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline CAS 5423-67-6 chemical structure

Description

The occurrence of 3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline 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.

3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline (CAS 5423-67-6), molecular formula C13H13NO and molecular weight 199.25 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 3-Hydroxy-1,2,3,4-tetrahydrobenzo[h]quinoline is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 199.25 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 FormulaC13H13NO
Molecular Weight199.25 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms1

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