2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol CAS 404925-69-5

Purity 97%+In StockPharmaceutical Standards
CAS No.404925-69-5
Molecular FormulaC17H16N2O
Molecular Weight264.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol CAS 404925-69-5 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 2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol.

CATO supplies 2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol (CAS 404925-69-5), a certified reference material (molecular formula C17H16N2O, MW 264.32 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, 2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 264.32 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), 2-(2,3,4,9-Tetrahydro-1h-pyrido[3,4-b]indol-1-yl)phenol 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 FormulaC17H16N2O
Molecular Weight264.32 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2

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