645-92-1

Basic information

• Product Name: AMMELINE
• Synonyms: 2,4-Diamino-1,3,5-triazin-6-one;4,6-Diamino-1,3,5-triazin-2(1H)-one;4,6-Diamino-1,3,5-triazin-2-ol;5-triazin-2(1h)-one,4,6-diamino-3;Ammelin;Ammeline, (4,6-diamino-5-triazin-2-ol);s-Triazin-2-ol, 4,6-diamino-;4,6-DIAMINO-2-HYDROXY-1,3,5-TRIAZINE
• CAS NO: 645-92-1
• Molecular Formula: C₃H₅N₅O
• Molecular Weight: 127.1
• EINECS: 211-455-1
• Product Categories: Bases & Related Reagents;Heterocycles;Nucleotides
• Mol File: 645-92-1.mol
• Article Data: 15

Chemical Properties

• Melting Point: >300?C (dec.)
• Boiling Point: 235.85°C (rough estimate)
• Flash Point: 136 °C
• Appearance: /
• Density: 1.4887 (rough estimate)
• Vapor Pressure: 6.62E-09mmHg at 25°C
• Refractive Index: 1.8000 (estimate)
• Storage Temp.: Refrigerator
• Solubility: Aqueous Base (Slightly)
• PKA: 6.20±0.70(Predicted)
• Water Solubility: 75mg/L(23 oC)
• BRN: 5570
• CAS DataBase Reference: AMMELINE(CAS DataBase Reference)
• NIST Chemistry Reference: AMMELINE(645-92-1)
• EPA Substance Registry System: AMMELINE(645-92-1)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 645-92-1(Hazardous Substances Data)

Usage

Description

AMMELINE, a metabolite of Melamine, is a white solid substance that serves as a non-protein nitrogen food additive. It is also found in pet foods and has been identified as a drinking water contaminant candidate by the United States Environmental Protection Agency (EPA). As a related compound of Melamine, AMMELINE is classified as an environmental and food contaminant.

Uses

Used in Food Industry:
AMMELINE is used as a non-protein nitrogen food additive for enhancing the nutritional value of certain products.
Used in Pet Food Industry:
AMMELINE is utilized in the pet food industry, contributing to the overall nutritional content of pet food products.
Used in Environmental Contaminant Research:
As a drinking water contaminant candidate listed on the EPA's CCL 3, AMMELINE is studied for its potential impact on the environment and human health, aiding in the development of regulations and safety measures.

InChI:InChI=1/C3H5N5O/c4-1-2(5)6-8-7-3(1)9/h(H2,4,8)(H3,5,6,7,9)

Upstream product

• 108-78-1 2,4,6-triamino-s-triazine 
• 57-13-6 urea 
• 127099-85-8 dicyandiamide 
• 1912-24-9 6-chloro-N-ethyl-N'-isopropyl-1,3,5-triazine-2,4-diamine 
• 122-34-9 Simazine 
• 5915-41-3 terbuthylazine 
• 884-43-5 2,4,6-triethoxy-[1,3,5]triazine 
• 3576-88-3 Melam 
• 448245-52-1 1-buthyl-3-methylimidazolium dicyanamide 
• 1934-75-4 sodium dicyanamide 
• 75-13-8 isocyanic acid 
• 590-28-3 potassium cyanate 
• 5470-11-1 hydroxylamine hydrochloride 
• 674-81-7 nitrosoguanidine 

Downstream Products

• 645-93-2 ammelide 
• 108-80-5 cyanuric acid 
• 19899-83-3 4,6-dihydrazino-1H-[1,3,5]triazin-2-one 
• 108-80-5 isocyanuric acid 
• 3397-62-4 2-Chloro-4,6-diamino-1,3,5-triazine 
• 590-28-3 potassium cyanate 
• 7664-41-7 ammonia 

Relevant articles and documents

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Preparation method of cyromazine

The invention discloses a preparation method of cyromazine. Melamine is used as an initial raw material; the preparation method comprises the following steps: carrying out an acidic hydrolysis reaction to obtain 4, 6-diamino-2-hydroxy-1, 3, 5-triazine, carrying out a chlorination reaction on 4, 6-diamino-2-hydroxy-1, 3, 5-triazine to obtain a toluene solution of 4, 6-diamino-2-chloro-1, 3, 5-triazine, and carrying out an amination reaction on 4, 6-diamino-2-chloro-1, 3, 5-triazine and cyclopropylamine so as to generate cyromazine. According to the method, toxic 2-cyclopropylamino-4, 6-dichloro-S-triazine is prevented from being generated, ammoniation pressurizing equipment is prevented from being used, reaction conditions are milder, cheaper materials are used, and the prepared cyclopropylamine is high in yield and good in quality.

Oxidation of atrazine by photoactivated potassium persulfate in aqueous solutions

General laws of the photochemical oxidation of atrazine by inorganic peroxo compounds under the impact of solar radiation are studied. It is found that almost complete conversion of atrazine can be achieved via photochemical oxidation with persulfate afte