1-Cyclohexyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 69743-49-3

Purity 97%+In StockPharmaceutical Standards
CAS No.69743-49-3
Molecular FormulaC17H25NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Cyclohexyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 69743-49-3 chemical structure

Description

CATO manufactures 1-Cyclohexyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 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.

1-Cyclohexyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (CAS 69743-49-3) is a high-purity analytical reference standard with the molecular formula C17H25NO2HCl and a molecular weight of 311.85 g/mol.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, 1-Cyclohexyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 311.85 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC17H25NO2 HCl
Molecular Weight311.85 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1976
Halogen ContentCl-containing
Nitrogen Atoms1

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