4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline CAS 88422-89-3

Purity 97%+In StockPharmaceutical Standards
CAS No.88422-89-3
Molecular FormulaC17H17N
Molecular Weight235.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline CAS 88422-89-3 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 4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline.

4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline (CAS 88422-89-3) is a high-purity analytical reference standard with the molecular formula C17H17N and a molecular weight of 235.32 g/mol.

Structurally, 4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline (C17H17N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 235.32 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).

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.

As a certified reference material (CRM), 4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline 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 FormulaC17H17N
Molecular Weight235.32 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms1

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