tert-Butyl (3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)carbamate CAS 257892-44-7

Purity 97%+In StockPharmaceutical Standards
CAS No.257892-44-7
Molecular FormulaC21H24F3NO3
Molecular Weight395.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)carbamate CAS 257892-44-7 chemical structure

Description

CATO supplies tert-Butyl (3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)carbamate (CAS 257892-44-7), a certified reference material (molecular formula C21H24F3NO3, MW 395.42 g/mol) for analytical method development and quality control.

tert-Butyl (3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)carbamate (C21H24F3NO3) contains a steroid core, 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, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), tert-Butyl (3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)carbamate 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 FormulaC21H24F3NO3
Molecular Weight395.42 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1

Recommended Standards

Why CATO?