4-(4-tert-Butylphenyl)-2-{[(4-methoxyphenyl)methyl]amino}-4-oxobutanoic acid CAS 1042722-13-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1042722-13-3
Molecular FormulaC22H27NO4
Molecular Weight369.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-tert-Butylphenyl)-2-{[(4-methoxyphenyl)methyl]amino}-4-oxobutanoic acid CAS 1042722-13-3 chemical structure

Description

As a certified reference material (CRM), 4-(4-tert-Butylphenyl)-2-{[(4-methoxyphenyl)methyl]amino}-4-oxobutanoic acid 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.

4-(4-tert-Butylphenyl)-2-{[(4-methoxyphenyl)methyl]amino}-4-oxobutanoic acid (CAS 1042722-13-3), molecular formula C22H27NO4 and molecular weight 369.45 g/mol, is a CATO reference standard with documented purity and traceability.

4-(4-tert-Butylphenyl)-2-{[(4-methoxyphenyl)methyl]amino}-4-oxobutanoic acid (C22H27NO4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC22H27NO4
Molecular Weight369.45 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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