4-Iodo-3-(trifluoromethoxy)aniline CAS 851045-63-1

Purity 97%+In StockPharmaceutical Standards
CAS No.851045-63-1
Molecular FormulaC7H5F3INO
Molecular Weight303.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Iodo-3-(trifluoromethoxy)aniline CAS 851045-63-1 chemical structure

Description

CATO manufactures 4-Iodo-3-(trifluoromethoxy)aniline 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.

CATO supplies 4-Iodo-3-(trifluoromethoxy)aniline (CAS 851045-63-1), a certified reference material (molecular formula C7H5F3INO, MW 303.02 g/mol) for analytical method development and quality control.

The molecular framework of 4-Iodo-3-(trifluoromethoxy)aniline (C7H5F3INO) is characterized by an amide group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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

Physical & Chemical Properties

Molecular FormulaC7H5F3INO
Molecular Weight303.02 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/I-containing
Nitrogen Atoms1

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