2-Iodo-6-nitro-4-(trifluoromethyl)aniline CAS 543740-74-5

Purity 97%+In StockPharmaceutical Standards
CAS No.543740-74-5
Molecular FormulaC7H4F3IN2O2
Molecular Weight332.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Iodo-6-nitro-4-(trifluoromethyl)aniline CAS 543740-74-5 chemical structure

Description

CATO supplies 2-Iodo-6-nitro-4-(trifluoromethyl)aniline (CAS 543740-74-5), a certified reference material (molecular formula C7H4F3IN2O2, MW 332.02 g/mol) for analytical method development and quality control.

2-Iodo-6-nitro-4-(trifluoromethyl)aniline (C7H4F3IN2O2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, an aromatic ring system. It is notably hygroscopic, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), 2-Iodo-6-nitro-4-(trifluoromethyl)aniline 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 FormulaC7H4F3IN2O2
Molecular Weight332.02 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, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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.)1984
Halogen ContentF/I-containing
Nitrogen Atoms2

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