1,1,1-Trifluoro-4-isopropylimino-2-methyl-4-phenylbutane-2-ol CAS 430466-00-5

Purity 97%+In StockPharmaceutical Standards
CAS No.430466-00-5
Molecular FormulaC14H18F3NO
Molecular Weight273.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,1,1-Trifluoro-4-isopropylimino-2-methyl-4-phenylbutane-2-ol CAS 430466-00-5 chemical structure

Description

1,1,1-Trifluoro-4-isopropylimino-2-methyl-4-phenylbutane-2-ol (C14H18F3NO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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.

1,1,1-Trifluoro-4-isopropylimino-2-methyl-4-phenylbutane-2-ol (CAS 430466-00-5), molecular formula C14H18F3NO and molecular weight 273.29 g/mol, is a CATO reference standard with documented purity and traceability.

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 1,1,1-Trifluoro-4-isopropylimino-2-methyl-4-phenylbutane-2-ol 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 FormulaC14H18F3NO
Molecular Weight273.29 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1

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