(R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride CAS 41220-48-8

Purity 97%+In StockPharmaceutical Standards
CAS No.41220-48-8
Molecular FormulaC10H11NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride CAS 41220-48-8 chemical structure

Description

Based on its molecular formula C10H11NO2HCl, (R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride contains a nitrogen-containing heterocyclic scaffold, 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 213.66 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

(R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride (CAS 41220-48-8), molecular formula C10H11NO2HCl and molecular weight 213.66 g/mol, is a CATO reference standard with documented purity and traceability.

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 (R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride 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 FormulaC10H11NO2 HCl
Molecular Weight213.66 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1968
Halogen ContentCl-containing
Nitrogen Atoms1

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