2,2'-Iminobis[4,6-diamino-1,3,5-triazine]

Base Information

• Chemical Name: 2,2'-Iminobis[4,6-diamino-1,3,5-triazine]
• CAS No.: 3576-88-3
• Deprecated CAS: 855596-65-5
• Molecular Formula: C6H9 N11
• Molecular Weight: 235.211
• Hs Code.: 2933699090
• European Community (EC) Number: 222-695-1
• UNII: 763B6VP74S
• DSSTox Substance ID: DTXSID50957156
• Nikkaji Number: J32.994K
• Wikipedia: Melam_(chemistry)
• Wikidata: Q6811137
• Mol file: 3576-88-3.mol

Synonyms:3576-88-3;Melam;2,2'-IMINOBIS[4,6-DIAMINO-1,3,5-TRIAZINE];2,2'-Iminobis(4,6-diamino-1,3,5-triazine);n2-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine;EINECS 222-695-1;C6H9N11;763B6VP74S;2-N-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine;EC 222-695-1;2-N-(Diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine;1,3,5-Triazine-2,4,6-triamine, N-(4,6-diamino-1,3,5-triazin-2-yl)-;1,3,5-Triazine-2,4,6-triamine, N2-(4,6-diamino-1,3,5-triazin-2-yl)-;SCHEMBL31485;UNII-763B6VP74S;SCHEMBL13954371;SCHEMBL16282611;SCHEMBL22320157;DTXSID50957156;CCG-2310;C6-H9-N11;FT-0699731;EN300-218561;S-TRIAZINE, 2,2'-IMINOBIS(4,6-DIAMINO-;Q6811137;N2-(diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine

Chemical Property of 2,2'-Iminobis[4,6-diamino-1,3,5-triazine]

Chemical Property:

• Vapor Pressure: 0Pa at 25℃
• Boiling Point: 828.3°Cat760mmHg
• PKA: 8.2[at 20 ℃]
• Flash Point: 454.8°C
• PSA: 196.37000
• Density: 1.897g/cm³
• LogP: -2.07760
• Water Solubility.: 24.5mg/L at 20℃
• XLogP3: -1.2
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 2
• Exact Mass: 235.10423933
• Heavy Atom Count: 17
• Complexity: 204

Purity/Quality:

99.9% ^*data from raw suppliers

N2-(4,6-Diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1(=NC(=NC(=N1)NC2=NC(=NC(=N2)N)N)N)N

Technology Process of 2,2'-Iminobis[4,6-diamino-1,3,5-triazine]

There total 17 articles about 2,2'-Iminobis[4,6-diamino-1,3,5-triazine] which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

2,4,6-triamino-s-triazine (108-78-1,25778-04-5,94977-27-2) → melam (3576-88-3)

Guidance literature:

With toluene-4-sulfonic acid; at 290 ℃; for 2h; Product distribution / selectivity;

Reference yield:

ammonium thiocyanate (1147550-11-5) → 2,4,6-triamino-s-triazine (108-78-1,25778-04-5,94977-27-2) + Melam (3576-88-3)

Guidance literature:

at 250 ℃; rhodanwasserstoffsaeures Melamin entsteht;

Reference yield:

dicyandiamide (127099-85-8,780722-26-1) → 2,4,6-triamino-s-triazine (108-78-1,25778-04-5,94977-27-2) + cyanomelamine (3496-98-8) + melam (3576-88-3) + ammeline (645-92-1) + ammelide (645-93-2)

Guidance literature:

In diphenylether; byproducts: meleme, NH3; heating at absence or presence of ZnCl2 or substituted amine;

upstream raw materials:

N-Cyanoguanidine

2,4,6-triamino-s-triazine

dicyandiamide

sodium dicyanamide

Downstream raw materials:

2,4,6-triamino-s-triazine

ammeline

ammonia

isocyanuric acid

Refernces

• 1、 Lotsch, Bettina V.,Schnick, Wolfgang. "New light on an old story: Formation of melam during thermal condensation of melamine". . p. 4956 - 4968. Retrieved 2007.
• 2、 Kessler, Fabian K.,Schnick, Wolfgang. "From Heptazines to Triazines – On the Formation of Poly(triazine imide)". . p. 857 - 862. Retrieved 2019/05/24.