6-methyl-1-(4-methylphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl CAS 1431966-17-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1431966-17-4
Molecular FormulaC19H20N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-methyl-1-(4-methylphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl CAS 1431966-17-4 chemical structure

Description

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

6-methyl-1-(4-methylphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl (CAS 1431966-17-4) is a high-purity analytical reference standard with the molecular formula C19H20N2HCl and a molecular weight of 312.84 g/mol.

Structurally, 6-methyl-1-(4-methylphenyl)-2,3,4,9-tetrahydro-1H-beta-carboline,HCl (C19H20N2HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 312.84 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 6-methyl-1-(4-methylphenyl)-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.

Physical & Chemical Properties

Molecular FormulaC19H20N2 HCl
Molecular Weight312.84 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
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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