4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl CAS 886762-46-5

Purity 97%+In StockPharmaceutical Standards
CAS No.886762-46-5
Molecular FormulaC14H7F6I
Molecular Weight416.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl CAS 886762-46-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 416.10 g/mol gives 4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl (CAS 886762-46-5) is a high-purity analytical reference standard with the molecular formula C14H7F6I and a molecular weight of 416.10 g/mol.

Owing to fluorine/iodine substitution, a polycyclic aromatic system, 4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 416.10 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 4'-Iodo-3,5-bis(trifluoromethyl)-1,1'-biphenyl 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 FormulaC14H7F6I
Molecular Weight416.10 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/I-containing

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