1-(4-Methylnaphthyl) trifluoromethyl ketone CAS 886370-33-8

Purity 97%+In StockPharmaceutical Standards
CAS No.886370-33-8
Molecular FormulaC13H9F3O
Molecular Weight238.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Methylnaphthyl) trifluoromethyl ketone CAS 886370-33-8 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 1-(4-Methylnaphthyl) trifluoromethyl ketone.

CATO supplies 1-(4-Methylnaphthyl) trifluoromethyl ketone (CAS 886370-33-8), a certified reference material (molecular formula C13H9F3O, MW 238.21 g/mol) for analytical method development and quality control.

Owing to a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system, 1-(4-Methylnaphthyl) trifluoromethyl ketone is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 238.21 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 1-(4-Methylnaphthyl) trifluoromethyl ketone 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.

Physical & Chemical Properties

Molecular FormulaC13H9F3O
Molecular Weight238.21 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing

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