7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole CAS 1056625-33-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1056625-33-2
Molecular FormulaC12H14N2
Molecular Weight186.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole CAS 1056625-33-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 186.25 g/mol gives 7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (CAS 1056625-33-2), a certified reference material (molecular formula C12H14N2, MW 186.25 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H14N2, 7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 186.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 7-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole 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 FormulaC12H14N2
Molecular Weight186.25 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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