(3S,4S)-3,4,8-Trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one CAS 1290143-55-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1290143-55-3
Molecular FormulaC11H12O5
Molecular Weight224.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,4S)-3,4,8-Trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one CAS 1290143-55-3 chemical structure

Description

(3S,4S)-3,4,8-Trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one (C11H12O5) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies (3S,4S)-3,4,8-Trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one (CAS 1290143-55-3), a certified reference material (molecular formula C11H12O5, MW 224.21 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures (3S,4S)-3,4,8-Trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one 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.

Physical & Chemical Properties

Molecular FormulaC11H12O5
Molecular Weight224.21 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990

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