1,2,3,4-Tetrahydronaphthalene-1,4-diol CAS 19070-56-5

Purity 97%+In StockPharmaceutical Standards
CAS No.19070-56-5
Molecular FormulaC10H12O2
Molecular Weight164.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,3,4-Tetrahydronaphthalene-1,4-diol CAS 19070-56-5 chemical structure

Description

The occurrence of 1,2,3,4-Tetrahydronaphthalene-1,4-diol is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1,2,3,4-Tetrahydronaphthalene-1,4-diol (CAS 19070-56-5), molecular formula C10H12O2 and molecular weight 164.20 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1,2,3,4-Tetrahydronaphthalene-1,4-diol (C10H12O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC10H12O2
Molecular Weight164.20 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962

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