Methyl 3-(4-hydroxy-3-iodophenyl)propanoate CAS 53937-20-5

Purity 97%+In StockPharmaceutical Standards
CAS No.53937-20-5
Molecular FormulaC10H11IO3
Molecular Weight306.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(4-hydroxy-3-iodophenyl)propanoate CAS 53937-20-5 chemical structure

Description

Based on its molecular formula C10H11IO3, Methyl 3-(4-hydroxy-3-iodophenyl)propanoate 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 306.10 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Methyl 3-(4-hydroxy-3-iodophenyl)propanoate (CAS 53937-20-5) is a high-purity analytical reference standard with the molecular formula C10H11IO3 and a molecular weight of 306.10 g/mol.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Methyl 3-(4-hydroxy-3-iodophenyl)propanoate 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.

Physical & Chemical Properties

Molecular FormulaC10H11IO3
Molecular Weight306.10 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Halogen ContentI-containing

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