N-[1-(1-benzothiophen-2-yl)ethyl]hydroxylamine CAS 118564-89-9

Purity 97%+In StockPharmaceutical Standards
CAS No.118564-89-9
Molecular FormulaC10H11NOS
Molecular Weight193.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-[1-(1-benzothiophen-2-yl)ethyl]hydroxylamine CAS 118564-89-9 chemical structure

Description

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.

CATO supplies N-[1-(1-benzothiophen-2-yl)ethyl]hydroxylamine (CAS 118564-89-9), a certified reference material (molecular formula C10H11NOS, MW 193.27 g/mol) for analytical method development and quality control.

The molecular framework of N-[1-(1-benzothiophen-2-yl)ethyl]hydroxylamine (C10H11NOS) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC10H11NOS
Molecular Weight193.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1
Sulfur Atoms1

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