3,4-Dihydroisoquinoline-2(1H)-carboximidamide hydrochloride CAS 1131-66-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1131-66-4
Molecular FormulaC10H13N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dihydroisoquinoline-2(1H)-carboximidamide hydrochloride CAS 1131-66-4 chemical structure

Description

3,4-Dihydroisoquinoline-2(1H)-carboximidamide hydrochloride (CAS 1131-66-4), molecular formula C10H13N3HCl and molecular weight 211.69 g/mol, is a CATO reference standard with documented purity and traceability.

3,4-Dihydroisoquinoline-2(1H)-carboximidamide hydrochloride (C10H13N3HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 3,4-Dihydroisoquinoline-2(1H)-carboximidamide 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 FormulaC10H13N3 HCl
Molecular Weight211.69 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentCl-containing
Nitrogen Atoms3

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