4-(tert-Butyl)-3-iodophenol CAS 1243411-01-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1243411-01-9
Molecular FormulaC10H13IO
Molecular Weight276.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butyl)-3-iodophenol CAS 1243411-01-9 chemical structure

Description

The occurrence of 4-(tert-Butyl)-3-iodophenol is closely related to a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 4-(tert-Butyl)-3-iodophenol (CAS 1243411-01-9), a certified reference material (molecular formula C10H13IO, MW 276.11 g/mol) for analytical method development and quality control.

Owing to a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system, 4-(tert-Butyl)-3-iodophenol is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 276.11 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 4-(tert-Butyl)-3-iodophenol 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 FormulaC10H13IO
Molecular Weight276.11 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
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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