4-Iodo-3-isopropoxyphenol CAS 1243329-05-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1243329-05-6
Molecular FormulaC9H11IO2
Molecular Weight278.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Iodo-3-isopropoxyphenol CAS 1243329-05-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 278.09 g/mol gives 4-Iodo-3-isopropoxyphenol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 4-Iodo-3-isopropoxyphenol (CAS 1243329-05-6), a certified reference material (molecular formula C9H11IO2, MW 278.09 g/mol) for analytical method development and quality control.

Based on its molecular formula C9H11IO2, 4-Iodo-3-isopropoxyphenol 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 278.09 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).

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

CATO manufactures 4-Iodo-3-isopropoxyphenol 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 FormulaC9H11IO2
Molecular Weight278.09 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentI-containing

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