Methyl 1,2,3,4-Tetrahydroisoquinoline-7-carboxylate Hydrochloride CAS 220247-69-8

Purity 97%+In StockPharmaceutical Standards
CAS No.220247-69-8
Molecular FormulaC11H13NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 1,2,3,4-Tetrahydroisoquinoline-7-carboxylate Hydrochloride CAS 220247-69-8 chemical structure

Description

CATO manufactures Methyl 1,2,3,4-Tetrahydroisoquinoline-7-carboxylate 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.

Methyl 1,2,3,4-Tetrahydroisoquinoline-7-carboxylate Hydrochloride (CAS 220247-69-8), molecular formula C11H13NO2HCl and molecular weight 227.69 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Methyl 1,2,3,4-Tetrahydroisoquinoline-7-carboxylate Hydrochloride (C11H13NO2HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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.

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

Physical & Chemical Properties

Molecular FormulaC11H13NO2 HCl
Molecular Weight227.69 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-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.)2019
Halogen ContentCl-containing
Nitrogen Atoms1

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