5-(2-(Trifluoromethyl)phenyl)-1-indanone CAS 863479-28-1

Purity 97%+In StockPharmaceutical Standards
CAS No.863479-28-1
Molecular FormulaC16H11F3O
Molecular Weight276.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-(Trifluoromethyl)phenyl)-1-indanone CAS 863479-28-1 chemical structure

Description

The occurrence of 5-(2-(Trifluoromethyl)phenyl)-1-indanone is closely related to a hydroxyl group, an ether linkage, fluorine substitution, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

5-(2-(Trifluoromethyl)phenyl)-1-indanone (CAS 863479-28-1) is a high-purity analytical reference standard with the molecular formula C16H11F3O and a molecular weight of 276.25 g/mol.

Owing to a hydroxyl group, an ether linkage, fluorine substitution, a polycyclic aromatic system, 5-(2-(Trifluoromethyl)phenyl)-1-indanone is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 276.25 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), 5-(2-(Trifluoromethyl)phenyl)-1-indanone 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 FormulaC16H11F3O
Molecular Weight276.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing

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