3-[4-(tert-Butyl)-2-chlorophenoxy]azetidine CAS 1220027-67-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1220027-67-7
Molecular FormulaC13H18ClNO
Molecular Weight239.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[4-(tert-Butyl)-2-chlorophenoxy]azetidine CAS 1220027-67-7 chemical structure

Description

As a certified reference material (CRM), 3-[4-(tert-Butyl)-2-chlorophenoxy]azetidine 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.

3-[4-(tert-Butyl)-2-chlorophenoxy]azetidine (CAS 1220027-67-7), molecular formula C13H18ClNO and molecular weight 239.74 g/mol, is a CATO reference standard with documented purity and traceability.

3-[4-(tert-Butyl)-2-chlorophenoxy]azetidine (C13H18ClNO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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. 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.

Physical & Chemical Properties

Molecular FormulaC13H18ClNO
Molecular Weight239.74 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.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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Why CATO?