8-fluoro-1H,2H,3H,4H,5H-pyrido[4,3-b]indole CAS 39876-39-6

Purity 97%+In StockPharmaceutical Standards
CAS No.39876-39-6
Molecular FormulaC11H19FN2
Molecular Weight198.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-fluoro-1H,2H,3H,4H,5H-pyrido[4,3-b]indole CAS 39876-39-6 chemical structure

Description

The occurrence of 8-fluoro-1H,2H,3H,4H,5H-pyrido[4,3-b]indole is closely related to a nitrile group, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 8-fluoro-1H,2H,3H,4H,5H-pyrido[4,3-b]indole (CAS 39876-39-6), a certified reference material (molecular formula C11H19FN2, MW 198.28 g/mol) for analytical method development and quality control.

Structurally, 8-fluoro-1H,2H,3H,4H,5H-pyrido[4,3-b]indole (C11H19FN2) contains a nitrile group, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 198.28 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 8-fluoro-1H,2H,3H,4H,5H-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 FormulaC11H19FN2
Molecular Weight198.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1968
Halogen ContentF-containing
Nitrogen Atoms2

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