1H,2H,3H,4H,9H-pyrido[3,4-b]indole hydrochloride CAS 58911-02-7

Purity 97%+In StockPharmaceutical Standards
CAS No.58911-02-7
Molecular FormulaC11H12N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1H,2H,3H,4H,9H-pyrido[3,4-b]indole hydrochloride CAS 58911-02-7 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 1H,2H,3H,4H,9H-pyrido[3,4-b]indole hydrochloride.

1H,2H,3H,4H,9H-pyrido[3,4-b]indole hydrochloride (CAS 58911-02-7) is a high-purity analytical reference standard with the molecular formula C11H12N2HCl and a molecular weight of 208.69 g/mol.

Structurally, 1H,2H,3H,4H,9H-pyrido[3,4-b]indole hydrochloride (C11H12N2HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 208.69 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H12N2 HCl
Molecular Weight208.69 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Halogen ContentCl-containing
Nitrogen Atoms2

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