2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine Dihydrochloride CAS 6000-50-6

Purity 97%+In StockPharmaceutical Standards
CAS No.6000-50-6
Molecular FormulaC7H8N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine Dihydrochloride CAS 6000-50-6 chemical structure

Description

CATO manufactures 2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine Dihydrochloride 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.

2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine Dihydrochloride (CAS 6000-50-6) is a high-purity analytical reference standard with the molecular formula C7H8N2HCl and a molecular weight of 156.61 g/mol.

The molecular framework of 2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine Dihydrochloride (C7H8N2HCl) is characterized by a nitrile group, chlorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC7H8N2 2*HCl
Molecular Weight156.61 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentCl-containing
Nitrogen Atoms2

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