Tert-butyl 2-(2-cyanophenoxy)acetate CAS 609804-44-6

Purity 97%+In StockPharmaceutical Standards
CAS No.609804-44-6
Molecular FormulaC13H15NO3
Molecular Weight233.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 2-(2-cyanophenoxy)acetate CAS 609804-44-6 chemical structure

Description

As a certified reference material (CRM), Tert-butyl 2-(2-cyanophenoxy)acetate 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.

CATO supplies Tert-butyl 2-(2-cyanophenoxy)acetate (CAS 609804-44-6), a certified reference material (molecular formula C13H15NO3, MW 233.26 g/mol) for analytical method development and quality control.

The molecular framework of Tert-butyl 2-(2-cyanophenoxy)acetate (C13H15NO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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.

Physical & Chemical Properties

Molecular FormulaC13H15NO3
Molecular Weight233.26 g/mol
AppearanceOff-white to pale yellow crystalline powder
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; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms1

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