[1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline CAS 226-65-3

Purity 97%+In StockPharmaceutical Standards
CAS No.226-65-3
Molecular FormulaC18H12N4
Molecular Weight284.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline CAS 226-65-3 chemical structure

Description

The occurrence of [1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies [1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline (CAS 226-65-3), a certified reference material (molecular formula C18H12N4, MW 284.31 g/mol) for analytical method development and quality control.

[1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline (C18H12N4) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

As a certified reference material (CRM), [1,2,4,5]Tetrazino[3,2-a:6,5-a']diisoquinoline 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 FormulaC18H12N4
Molecular Weight284.31 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Nitrogen Atoms4

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