1-Benzyl 4-(tert-butyl) 6-amino-1,4-diazepane-1,4-dicarboxylate CAS 1508259-58-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1508259-58-2
Molecular FormulaC18H27N3O4
Molecular Weight349.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Benzyl 4-(tert-butyl) 6-amino-1,4-diazepane-1,4-dicarboxylate CAS 1508259-58-2 chemical structure

Description

The molecular framework of 1-Benzyl 4-(tert-butyl) 6-amino-1,4-diazepane-1,4-dicarboxylate (C18H27N3O4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

1-Benzyl 4-(tert-butyl) 6-amino-1,4-diazepane-1,4-dicarboxylate (CAS 1508259-58-2) is a high-purity analytical reference standard with the molecular formula C18H27N3O4 and a molecular weight of 349.42 g/mol.

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 FormulaC18H27N3O4
Molecular Weight349.42 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.)1992
Nitrogen Atoms3

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