7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole CAS 91566-22-2

Purity 97%+In StockPharmaceutical Standards
CAS No.91566-22-2
Molecular FormulaC12H14N2O
Molecular Weight202.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole CAS 91566-22-2 chemical structure

Description

The occurrence of 7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 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.

CATO supplies 7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole (CAS 91566-22-2), a certified reference material (molecular formula C12H14N2O, MW 202.25 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 202.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

As a certified reference material (CRM), 7-Methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H14N2O
Molecular Weight202.25 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.)1983
Nitrogen Atoms2

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