2,4,5,6-Tetraaminopyrimidine

Base Information

• Chemical Name: 2,4,5,6-Tetraaminopyrimidine
• CAS No.: 1004-74-6
• Molecular Formula: C4H8N6
• Molecular Weight: 140.148
• Hs Code.: 29335990
• European Community (EC) Number: 213-724-9
• UNII: 24FC717FE5
• DSSTox Substance ID: DTXSID9043807
• Nikkaji Number: J51.390C
• Wikidata: Q15726087
• ChEMBL ID: CHEMBL2151966
• Mol file: 1004-74-6.mol

Synonyms:2,4,5,6-Tetraaminopyrimidine;1004-74-6;Pyrimidinetetramine;pyrimidine-2,4,5,6-tetramine;Pyrimidine-2,4,5,6-Tetraamine;tetra-aminopyrimidine;2,4,5,6-Pyrimidinetetramine;Pyrimidine, 2,4,5,6-tetraamino-;tetraaminopyrimidine;BRN 0144442;2,4,5,6-Tetraaminopyrimidiine;EINECS 213-724-9;UNII-24FC717FE5;24FC717FE5;2,4,5,6-Tetraaminopyrimidine sulphate monohydrate;5-25-12-00377 (Beilstein Handbook Reference);C4H8N6;2,4,5,6-Pyrimidinetetraamine;SCHEMBL33841;2,4,5,6-tetraminopyrimidine;PYRIMIDINE, TETRAAMINO-;CHEMBL2151966;DTXSID9043807;2,4,5,6-Pyrimidinetetramine #;HY-D1061;BBL028285;STK935566;AKOS005665274;SB55973;2,4,5,6-TETRA AMINOPYRIMIDINE;(2,4,6-triamino-pyrimidin-5-yl)-amine;AC-26744;AS-59260;LS-135527;CS-0104923;FT-0633232;E80414;EN300-143670;Q15726087

Chemical Property of 2,4,5,6-Tetraaminopyrimidine

Chemical Property:

• Vapor Pressure: 1.64E-30mmHg at 25°C
• Boiling Point: 563.918 °C at 760 mmHg
• PKA: 6.97±0.10(Predicted)
• Flash Point: 329.383 °C
• PSA: 129.86000
• Density: 1.649 g/cm³
• LogP: 1.13020
• XLogP3: -1.5
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 140.08104428
• Heavy Atom Count: 10
• Complexity: 104

Purity/Quality:

2,4,5,6-Tetraaminopyrimidine 95+% ^*data from reagent suppliers

Safty Information:

• Statements: 20/22
• Safety Statements: 36/37

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1(=C(N=C(N=C1N)N)N)N

Technology Process of 2,4,5,6-Tetraaminopyrimidine

There total 5 articles about 2,4,5,6-Tetraaminopyrimidine 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:

5-nitroso-2,4,6-triaminopyrimidine (1006-23-1) → 2,4,5,6-tetraaminopyrimidine (1004-74-6)

Guidance literature:

With sodium dithionite; water;

DOI:10.1021/ja01199a073 DOI:10.1021/ja01147a027

Reference yield:

5-nitropyrimidine-2,4,6-triamine (24867-36-5) → 2,4,5,6-tetraaminopyrimidine (1004-74-6)

Guidance literature:

With hydrogenchloride; tin(ll) chloride;

Reference yield:

→ 2,4,5,6-tetraaminopyrimidine (1004-74-6)

Guidance literature:

Herstellung von <2-¹⁴C>Pyrimidintetrayltetraamin;

DOI:10.1021/ja01129a518

upstream raw materials:

5-nitroso-2,4,6-triaminopyrimidine

5-nitropyrimidine-2,4,6-triamine

hydrogenchloride

Downstream raw materials:

2,4-diamino-6-phenyl-7(8H)-pteridinone

{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-arsonic acid

2,4,6-Triamino-5-formylamino-pyrimidin

4-[(2,4-diaminopteridin-6-ylmethyl)methylamino]benzoic acid

Refernces

• 1、 Mallette et al.. "-". . p. 1814. Retrieved 1947.
• 2、 -. "1,3-Dihydroxybenzene derivatives and colorants containing said compounds". . . Retrieved 2008/06/13.
• 3、 -. "Transition metal complexes as dye forming catalysts in hair coloring compositions". . . Retrieved 2008/06/13.