Ammelide

Base Information

• Chemical Name: Ammelide
• CAS No.: 645-93-2
• Deprecated CAS: 3159-68-0,30196-41-9
• Molecular Formula: C3H4N4O2
• Molecular Weight: 128.09
• Hs Code.: 2933699090
• European Community (EC) Number: 211-456-7,803-297-2
• NSC Number: 8146
• UNII: J604QC4098
• DSSTox Substance ID: DTXSID10214757
• Nikkaji Number: J9.461G
• Wikipedia: Ammelide
• Wikidata: Q4747226
• Metabolomics Workbench ID: 51592
• Mol file: 645-93-2.mol

Synonyms:6-amino-1,3,5-triazine-2,4(1H,3H)-dione;ammelide;ammelide copper

Chemical Property of Ammelide

Chemical Property:

• Appearance/Colour: White Solid
• Melting Point: >300 °C(lit.)
• Refractive Index: 1.8010 (estimate)
• Boiling Point: 695.8 °C at 760 mmHg
• PKA: 7.22±0.10(Predicted)
• Flash Point: 374.6 °C
• PSA: 105.15000
• Density: 2.22 g/cm³
• LogP: -0.55380
• Storage Temp.: Refrigerator
• Solubility.: Aqueous Base (Very Slightly), DMSO (Very Slightly, Heated, Sonicated)
• Water Solubility.: 76.85mg/L(2 oC)
• XLogP3: -1.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 128.03342538
• Heavy Atom Count: 9
• Complexity: 196

Purity/Quality:

98%,99%, ^*data from raw suppliers

Ammelide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 43-36/37/38
• Safety Statements: 36/37-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1(=NC(=O)NC(=O)N1)N
• Uses: A stable labelled analogue of Melamine Ammelide, is a metabolite of Melamine (1) (M208700), which acts as a non-protein nitrogen food additive (2). Also present in pet foods as well (3).Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.

Technology Process of Ammelide

There total 82 articles about Ammelide 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: 34.0%

2-amino-4,6-diureido-1,3,5-triazine (90802-01-0) → ammelide (645-93-2) + uronium nitrate (124-47-0) + cyanuric acid melamine (37640-57-6) + isocyanuric acid (108-80-5)

Guidance literature:

With hydrogenchloride; Heating;

DOI:10.1246/bcsj.57.2009

Reference yield:

N,N',N''-(1,3,4,6,7,9,9b-heptaaza-phenalene-2,5,8-triyl)-tris-cyanamide (1593-03-9) → ammelide (645-93-2) + ammonia (7664-41-7) + cyamelluric acid (1502-46-1)

Guidance literature:

dann spaltet sich das Ammelid in Ammoniak und Melanurensaeure und zuletzt in Cyanursaeure;

Reference yield:

N-Cyanoguanidine (127099-85-8,780722-26-1,461-58-5) → ammelide (645-93-2) + guanidine hydrochloride (50-01-1) + BIGUANIDE (56-03-1)

Guidance literature:

at 150 ℃;

DOI:10.1177/004051750107100714

upstream raw materials:

phosgene

cyanuric bromide

urea

2,4,6-triamino-s-triazine

Downstream raw materials:

1,3,5-trichloro-2,4,6-triazine

CYANAMID

carbonic-acid

ammonia

Refernces

• 1、 Zavyalov,Polchvisneva. "-". . . Retrieved 1973.
• 2、 Chan, Cho Yin,Chan, Ho Shing,Wong, Po Keung. "Integrated photocatalytic-biological treatment of triazine-containing pollutants". . p. 371 - 380. Retrieved 2019/02/07.
• 3、 Le Cunff, Jér?me,Toma?i?, Vesna,Wittine, Ozren. "Photocatalytic degradation of the herbicide terbuthylazine: Preparation, characterization and photoactivity of the immobilized thin layer of TiO2/chitosan". . p. 22 - 29. Retrieved 2015/05/13.