1-(4-Chloro-3-fluoro-2-iodo-phenyl)-4-(trifluoromethyl)triazole CAS 2097065-63-7

Purity 97%+In StockPharmaceutical Standards
CAS No.2097065-63-7
Molecular FormulaC9H3ClF4IN3
Molecular Weight391.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Chloro-3-fluoro-2-iodo-phenyl)-4-(trifluoromethyl)triazole CAS 2097065-63-7 chemical structure

Description

1-(4-Chloro-3-fluoro-2-iodo-phenyl)-4-(trifluoromethyl)triazole (C9H3ClF4IN3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine/iodine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

1-(4-Chloro-3-fluoro-2-iodo-phenyl)-4-(trifluoromethyl)triazole (CAS 2097065-63-7) is a high-purity analytical reference standard with the molecular formula C9H3ClF4IN3 and a molecular weight of 391.49 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 1-(4-Chloro-3-fluoro-2-iodo-phenyl)-4-(trifluoromethyl)triazole 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 FormulaC9H3ClF4IN3
Molecular Weight391.49 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentF/Cl/I-containing
Nitrogen Atoms3

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