3-(4-Methyl-1h-indol-3-yl)-3-oxopropanenitrile CAS 1020091-69-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1020091-69-3
Molecular FormulaC12H10N2O
Molecular Weight198.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Methyl-1h-indol-3-yl)-3-oxopropanenitrile CAS 1020091-69-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-(4-Methyl-1h-indol-3-yl)-3-oxopropanenitrile.

CATO supplies 3-(4-Methyl-1h-indol-3-yl)-3-oxopropanenitrile (CAS 1020091-69-3), a certified reference material (molecular formula C12H10N2O, MW 198.22 g/mol) for analytical method development and quality control.

The molecular framework of 3-(4-Methyl-1h-indol-3-yl)-3-oxopropanenitrile (C12H10N2O) 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.

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

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 FormulaC12H10N2O
Molecular Weight198.22 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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