3047-33-4

Basic information

• Product Name: Cyanuric acid trisodium salt
• Synonyms: 1,3,5-triazine-2,4,6(1H,3H,5H)-trione, trisodium salt;Cyanuric acid trisodium salt
• CAS NO: 3047-33-4
• Molecular Formula: C₃N₃O₃*3Na
• Molecular Weight: 195.02
• EINECS: 221-255-6
• Mol File: 3047-33-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: >330oC
• Appearance: /
• Density: 2.09[at 20℃]
• Water Solubility: 1000g/L at 25℃
• CAS DataBase Reference: Cyanuric acid trisodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Cyanuric acid trisodium salt(3047-33-4)
• EPA Substance Registry System: Cyanuric acid trisodium salt(3047-33-4)

Safety Data

• Hazardous Substances Data: 3047-33-4(Hazardous Substances Data)

Usage

General Description

Cyanuric acid trisodium salt, also known as sodium tricyanurate, is a chemical compound that is commonly used as a stabilizer in swimming pools to prevent the degradation of chlorine from sunlight. It is a white, odorless, and water-soluble solid that is derived from cyanuric acid, which is a triazine derivative. Cyanuric acid trisodium salt works by forming a complex with chlorine molecules, protecting them from breaking down and allowing them to remain effective in sanitizing the pool water. It is generally considered safe when used in recommended concentrations, but overuse can lead to the buildup of cyanuric acid in pool water, which can reduce the effectiveness of chlorine and lead to potential health and environmental risks.

InChI:InChI=1/C3H3N3O3.3Na/c7-1-4-2(8)6-3(9)5-1;;;/h(H3,4,5,6,7,8,9);;;/q;3*+1

Upstream product

• 108-80-5 isocyanuric acid 
• 1310-73-2 sodium hydroxide 
• 108-80-5 cyanuric acid 

Downstream Products

• 6291-95-8 tris-2-methylprop-2-en-1-ylisocyanurate 
• 40601-76-1 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate 
• 1025-15-6 triallyl isocyanurate 
• 87-90-1 trichloroisocyanuric acid 

Relevant articles and documents

2,2′,2″-(2,4,6-Trioxo-1,3,5-triazinane-1,3,5-triyl)triacetic Acid Derivatives. New Aspects of Reactivity

Abstract: Reaction of 2,2′,2″-(2,4,6-trioxo-1,3,5-triazinane-1,3,5-triyl)triacetic acid derivatives with nucleophiles in aqueous medium involved opening of the triazinane ring with elimination of carbonyl group, followed by recyclization to 1-carbamoylhydantoins.

Photosensitive resin composition for color filter and uses thereof

The present invention relates to a photosensitive resin composition for a color filter and uses thereof. The photosensitive resin composition includes an alkali-soluble resin (A), a compound (B) containing an ethylenically unsaturated group, a photoinitiator (C), a pigment (D) and an organic solvent (E). The photosensitive resin composition according to the present invention can improve linearity of pattern with high finesse and developing-resistance of the color filter.

HIGHLY CONCENTRATED BROMINE COMPOSITIONS AND METHODS OF PREPARATION

Liquid and solid bromine-containing compositions are described. A liquid mixed halogen composition is also described. The highly concentrated liquid compositions and the high-activity solid compositions have excellent physical and chemical stability. The compositions are effective biocides in water treatment. Methods of preparing the compositions are also disclosed. These include combining a bromine compound in the oxidation state of -1 with hydrogen peroxide and a complexing agent followed by the addition of an alkaline source. The methods may further include the use of a solid organic or solid inorganic halogenating agent, conducting a solid-liquid separation, and adding an alkaline source.