5-(Tert-butyl)-2-(piperazin-1-ylmethyl)oxazole CAS 1094682-32-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1094682-32-2
Molecular FormulaC12H21N3O
Molecular Weight223.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(Tert-butyl)-2-(piperazin-1-ylmethyl)oxazole CAS 1094682-32-2 chemical structure

Description

The occurrence of 5-(Tert-butyl)-2-(piperazin-1-ylmethyl)oxazole is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

5-(Tert-butyl)-2-(piperazin-1-ylmethyl)oxazole (CAS 1094682-32-2) is a high-purity analytical reference standard with the molecular formula C12H21N3O and a molecular weight of 223.31 g/mol.

The molecular framework of 5-(Tert-butyl)-2-(piperazin-1-ylmethyl)oxazole (C12H21N3O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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.

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 FormulaC12H21N3O
Molecular Weight223.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms3

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