N-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-2-isopropoxyaniline CAS 1040682-70-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1040682-70-9
Molecular FormulaC19H24ClNO2
Molecular Weight333.85 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-2-isopropoxyaniline CAS 1040682-70-9 chemical structure

Description

Structurally, N-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-2-isopropoxyaniline (C19H24ClNO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 333.85 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies N-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-2-isopropoxyaniline (CAS 1040682-70-9), a certified reference material (molecular formula C19H24ClNO2, MW 333.85 g/mol) for analytical method development and quality control.

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 N-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-2-isopropoxyaniline 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 FormulaC19H24ClNO2
Molecular Weight333.85 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms1

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