AMMELINE

Base Information

• Chemical Name: AMMELINE
• CAS No.: 645-92-1
• Molecular Formula: C3H5N5O
• Molecular Weight: 127.106
• Hs Code.: 2933699090
• Mol file: 645-92-1.mol

Synonyms:Ammeline(6CI);2,4-Diamino-6-hydroxy-1,3,5-triazine;2,4-Diamino-6-hydroxy-s-triazine;2-Hydroxy-4,6-diamino-s-triazine;2-Hydroxydesethyldesisopropylatrazine;4,6-Diamino-2-hydroxy-s-triazine;Ammelin;Deethyldeisopropylhydroxyyatrazine;GS 11791;NSC 9778;s-Diaminohydroxytriazine;s-Triazin-2-ol, 4,6-diamino-(8CI);2,4-Diamino-1,3,5-triazin-6-one;s-Triazin-2(1H)-one, 4,6-diamino- (7CI);

Chemical Property of AMMELINE

Chemical Property:

• Vapor Pressure: 6.62E-09mmHg at 25°C
• Melting Point: >300?C (dec.)
• Refractive Index: 1.802
• Boiling Point: 301.2 °C at 760 mmHg
• PKA: 6.20±0.70(Predicted)
• Flash Point: 136 °C
• PSA: 110.94000
• Density: 2.22 g/cm³
• LogP: -0.09600
• Storage Temp.: Refrigerator
• Solubility.: Aqueous Base (Slightly)
• Water Solubility.: 75mg/L(23 oC)

Purity/Quality:

98% ^*data from raw suppliers

Ammeline ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Ammeline 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. A related compound of Melamine.

Technology Process of AMMELINE

There total 80 articles about AMMELINE 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: 43.0%

2,4,6-triureido-1,3,5-triazine (4801-02-9) → ammeline (645-92-1)

Guidance literature:

With alkaline hydrolysis;

DOI:10.1246/bcsj.57.2009

Reference yield: 33.0%

2-amino-4,6-diureido-1,3,5-triazine (90802-01-0) → 2,4,6-triamino-s-triazine (108-78-1,25778-04-5,94977-27-2) + ammeline (645-92-1)

Guidance literature:

With alkaline hydrolysis;

DOI:10.1246/bcsj.57.2009

Reference yield:

nitrosoguanidine (674-81-7) + ammonia (7664-41-7) → 2,4,6-triamino-s-triazine (108-78-1,25778-04-5,94977-27-2) + ammelide (645-93-2) + guanidine nitrate (113-00-8) + ammeline (645-92-1) + urea (57-13-6)

Guidance literature:

In water; heating under reflux;

DOI:10.1021/ja01290a008

upstream raw materials:

Melam

2,4,6-triethoxy-[1,3,5]triazine

guanidine; formate

BIGUANIDE

Downstream raw materials:

ammelide

cyanuric acid

4,6-dihydrazino-1H-[1,3,5]triazin-2-one

isocyanuric acid

Refernces

• 1、 Wang, Chao,Fan, Huiqing,Ren, Xiaohu,Ma, Jiangwei,Fang, Jiawen,Wang, Weijia. "Hydrothermally Induced Oxygen Doping of Graphitic Carbon Nitride with a Highly Ordered Architecture and Enhanced Photocatalytic Activity". . p. 700 - 708. Retrieved 2018.
• 2、 Song, Chunli,Zhan, Qing,Liu, Fei,Wang, Chuan,Li, Hongchao,Wang, Xuan,Guo, Xuefeng,Cheng, Yingchun,Sun, Wei,Wang, Li,Qian, Jieshu,Pan, Bingcai. "Overturned Loading of Inert CeO2 to Active Co3O4 for Unusually Improved Catalytic Activity in Fenton-Like Reactions". supporting information. . Retrieved 2022/02/23.
• 3、 Chan, Cho Yin,Chan, Ho Shing,Wong, Po Keung. "Integrated photocatalytic-biological treatment of triazine-containing pollutants". . p. 371 - 380. Retrieved 2019/02/07.