(E)-3-(Naphthalen-1-yl)acrylic acid CAS 2006-14-6

Purity 97%+In StockPharmaceutical Standards
CAS No.2006-14-6
Molecular FormulaC13H10O2
Molecular Weight198.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-3-(Naphthalen-1-yl)acrylic acid CAS 2006-14-6 chemical structure

Description

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.

CATO supplies (E)-3-(Naphthalen-1-yl)acrylic acid (CAS 2006-14-6), a certified reference material (molecular formula C13H10O2, MW 198.22 g/mol) for analytical method development and quality control.

The molecular framework of (E)-3-(Naphthalen-1-yl)acrylic acid (C13H10O2) 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.

Physical & Chemical Properties

Molecular FormulaC13H10O2
Molecular Weight198.22 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

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