3-(3-Ethoxy-5-iodo-4-methoxyphenyl)acrylic acid CAS 340216-06-0

Purity 97%+In StockPharmaceutical Standards
CAS No.340216-06-0
Molecular FormulaC12H13IO4
Molecular Weight348.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(3-Ethoxy-5-iodo-4-methoxyphenyl)acrylic acid CAS 340216-06-0 chemical structure

Description

3-(3-Ethoxy-5-iodo-4-methoxyphenyl)acrylic acid (CAS 340216-06-0), molecular formula C12H13IO4 and molecular weight 348.13 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C12H13IO4, 3-(3-Ethoxy-5-iodo-4-methoxyphenyl)acrylic acid contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 348.13 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 3-(3-Ethoxy-5-iodo-4-methoxyphenyl)acrylic acid 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 FormulaC12H13IO4
Molecular Weight348.13 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing

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