(5-Iodo-2-methoxyphenyl)methanol CAS 197916-95-3

Purity 97%+In StockPharmaceutical Standards
CAS No.197916-95-3
Molecular FormulaC8H9IO2
Molecular Weight264.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-Iodo-2-methoxyphenyl)methanol CAS 197916-95-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 264.06 g/mol gives (5-Iodo-2-methoxyphenyl)methanol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (5-Iodo-2-methoxyphenyl)methanol (CAS 197916-95-3), a certified reference material (molecular formula C8H9IO2, MW 264.06 g/mol) for analytical method development and quality control.

(5-Iodo-2-methoxyphenyl)methanol (C8H9IO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 (5-Iodo-2-methoxyphenyl)methanol 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 FormulaC8H9IO2
Molecular Weight264.06 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.)2013
Halogen ContentI-containing

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