6-Tert-butyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 404576-48-3

Purity 97%+In StockPharmaceutical Standards
CAS No.404576-48-3
Molecular FormulaC13H19N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Tert-butyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 404576-48-3 chemical structure

Description

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

CATO supplies 6-Tert-butyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (CAS 404576-48-3), a certified reference material (molecular formula C13H19NHCl, MW 225.76 g/mol) for analytical method development and quality control.

Structurally, 6-Tert-butyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (C13H19NHCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 225.76 g/mol, it falls into the medium-molecular-weight range. 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).

As a certified reference material (CRM), 6-Tert-butyl-1,2,3,4-tetrahydroisoquinoline hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC13H19N HCl
Molecular Weight225.76 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.)2025
Halogen ContentCl-containing
Nitrogen Atoms1

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