2-((tert-Butoxycarbonyl)amino)-2-(4-((tert-butoxycarbonyl)amino)phenyl)acetic acid CAS 88197-41-5

Purity 97%+In StockPharmaceutical Standards
CAS No.88197-41-5
Molecular FormulaC18H26N2O6
Molecular Weight366.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((tert-Butoxycarbonyl)amino)-2-(4-((tert-butoxycarbonyl)amino)phenyl)acetic acid CAS 88197-41-5 chemical structure

Description

CATO supplies 2-((tert-Butoxycarbonyl)amino)-2-(4-((tert-butoxycarbonyl)amino)phenyl)acetic acid (CAS 88197-41-5), a certified reference material (molecular formula C18H26N2O6, MW 366.41 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, 2-((tert-Butoxycarbonyl)amino)-2-(4-((tert-butoxycarbonyl)amino)phenyl)acetic acid is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 366.41 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H26N2O6
Molecular Weight366.41 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 DMSO, DMF, methanol
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.)1982
Nitrogen Atoms2

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