6-Bromo-4-ethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 1243382-67-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1243382-67-3
Molecular FormulaC11H14BrN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Bromo-4-ethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 1243382-67-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 6-Bromo-4-ethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride.

6-Bromo-4-ethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (CAS 1243382-67-3) is a high-purity analytical reference standard with the molecular formula C11H14BrNHCl and a molecular weight of 276.60 g/mol.

6-Bromo-4-ethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (C11H14BrNHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine/bromine 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. 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.

CATO manufactures 6-Bromo-4-ethyl-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.

Physical & Chemical Properties

Molecular FormulaC11H14BrN HCl
Molecular Weight276.60 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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