4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one CAS 37574-74-6

Purity 97%+In StockPharmaceutical Standards
CAS No.37574-74-6
Molecular FormulaC11H9N3O
Molecular Weight199.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one CAS 37574-74-6 chemical structure

Description

The occurrence of 4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one 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.

4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one (CAS 37574-74-6) is a high-purity analytical reference standard with the molecular formula C11H9N3O and a molecular weight of 199.21 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 199.21 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 4-methyl[1,2,4]triazino[4,5-a]indol-1(2H)-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H9N3O
Molecular Weight199.21 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.)1967
Nitrogen Atoms3

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