Ethyl (2-ethoxy-4-formyl-6-iodophenoxy)acetate CAS 428837-88-1

Purity 97%+In StockPharmaceutical Standards
CAS No.428837-88-1
Molecular FormulaC13H15IO5
Molecular Weight378.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl (2-ethoxy-4-formyl-6-iodophenoxy)acetate CAS 428837-88-1 chemical structure

Description

As a certified reference material (CRM), Ethyl (2-ethoxy-4-formyl-6-iodophenoxy)acetate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Ethyl (2-ethoxy-4-formyl-6-iodophenoxy)acetate (CAS 428837-88-1), molecular formula C13H15IO5 and molecular weight 378.16 g/mol, is a CATO reference standard with documented purity and traceability.

Ethyl (2-ethoxy-4-formyl-6-iodophenoxy)acetate (C13H15IO5) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC13H15IO5
Molecular Weight378.16 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 methanol, acetonitrile, DMSO, water (slightly soluble)
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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