tert-Butyl N-[(5-hydroxythiophen-2-yl)methyl]carbamate CAS 1881288-19-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1881288-19-2
Molecular FormulaC10H15NO3S
Molecular Weight229.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl N-[(5-hydroxythiophen-2-yl)methyl]carbamate CAS 1881288-19-2 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies tert-Butyl N-[(5-hydroxythiophen-2-yl)methyl]carbamate (CAS 1881288-19-2), a certified reference material (molecular formula C10H15NO3S, MW 229.30 g/mol) for analytical method development and quality control.

The molecular framework of tert-Butyl N-[(5-hydroxythiophen-2-yl)methyl]carbamate (C10H15NO3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone 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.

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 FormulaC10H15NO3S
Molecular Weight229.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms1
Sulfur Atoms1

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