Description

Triphenylene-2,3,6,7,10,11-hexaamine hexahydrochloride (CAS: 1350518-27-2) is a high-purity organic compound with the molecular formula C₁₈H₂₄Cl₆N₆. This aromatic amine derivative features a triphenylene core functionalized with six primary amine groups, each protonated as a hydrochloride salt for enhanced stability and solubility. The compound is supplied as a crystalline solid with consistent batch-to-batch purity, verified by advanced analytical techniques including HPLC, NMR, and mass spectrometry. Ideal for materials science and coordination chemistry applications, this building block enables precise synthesis of covalent organic frameworks (COFs), metal-organic frameworks (MOFs), and conductive polymers. Strict quality control ensures low heavy metal content (<10 ppm) and suitability for sensitive electrochemical or optoelectronic research.

Properties

• CAS Number: 1350518-27-2
• Complexity: 364
• IUPAC Name: triphenylene-2,3,6,7,10,11-hexamine;hexahydrochloride
• InChI: InChI=1S/C18H18N6.6ClH/c19-13-1-7-8(2-14(13)20)10-4-17(23)18(24)6-12(10)11-5-16(22)15(21)3-9(7)11;;;;;;/h1-6H,19-24H2;6*1H
• InChI Key: PUXBEKLSMBVFNW-UHFFFAOYSA-N
• Exact Mass: 536.016411
• Molecular Formula: C18H24Cl6N6
• Molecular Weight: 537.1
• SMILES: C1=C2C3=CC(=C(C=C3C4=CC(=C(C=C4C2=CC(=C1N)N)N)N)N)N.Cl.Cl.Cl.Cl.Cl.Cl
• Topological: 156
• Monoisotopic Mass: 534.019361
• Synonyms: 1350518-27-2, Triphenylene-2,3,6,7,10,11-hexaamine hexahydrochloride, 2,3,6,7,10,11-Triphenylenehexamine, 2,3,6,7,10,11-hexaaminotriphenylene hexahydrochloride, HATP, YSZC091, SCHEMBL18606145, AC9808, AKOS037651884, CS-17536, FT157078, TRIPHENYLENE-2,3,6,7,10,11-HEXAAMINE 6HCL, 2,3,6,7,10,11-Triphenylenehexamine hexahydrochloride, Triphenylene-2,3,6,7,10,11-hexaaminehexahydrochloride

Triphenylene-2,3,6,7,10,11-hexaamine hexahydrochloride serves as a key precursor for nitrogen-rich porous materials in gas storage applications. Researchers utilize its multiple coordination sites to construct 2D conductive polymers for organic electronics. The compound shows promise in developing next-generation battery electrolytes due to its redox-active amine groups. Catalysis studies employ this reagent to anchor transition metals in molecular scaffolding. Its planar aromatic structure makes it valuable for organic semiconductor research.

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