N-{2-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline CAS 1040691-12-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1040691-12-0
Molecular FormulaC23H33NO2
Molecular Weight355.51 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-{2-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline CAS 1040691-12-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 355.51 g/mol gives N-{2-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-{2-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline (CAS 1040691-12-0), a certified reference material (molecular formula C23H33NO2, MW 355.51 g/mol) for analytical method development and quality control.

Structurally, N-{2-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline (C23H33NO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. 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 355.51 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-[2,4-Di(tert-butyl)phenoxy]ethyl}-3-methoxyaniline 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 FormulaC23H33NO2
Molecular Weight355.51 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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