6-methoxy-1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl CAS 1431967-99-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1431967-99-5
Molecular FormulaC19H20N2O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-methoxy-1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl CAS 1431967-99-5 chemical structure

Description

As a certified reference material (CRM), 6-methoxy-1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl 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.

6-methoxy-1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl (CAS 1431967-99-5) is a high-purity analytical reference standard with the molecular formula C19H20N2O2HCl and a molecular weight of 344.84 g/mol.

Based on its molecular formula C19H20N2O2HCl, 6-methoxy-1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 344.84 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC19H20N2O2 HCl
Molecular Weight344.84 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms2

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