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Cyanuric acid trisodium salt, also known as sodium tricyanurate, is a white, odorless, and water-soluble solid derived from cyanuric acid, a triazine derivative. It is commonly used as a stabilizer in swimming pools to prevent the degradation of chlorine from sunlight, forming a complex with chlorine molecules and allowing them to remain effective in sanitizing the pool water.

3047-33-4

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3047-33-4 Usage

Uses

Used in Swimming Pool Industry:
Cyanuric acid trisodium salt is used as a stabilizer to prevent the degradation of chlorine from sunlight, ensuring the effectiveness of chlorine in sanitizing pool water. It helps maintain the recommended concentration of chlorine, promoting a clean and safe swimming environment.
Cyanuric acid trisodium salt is used as a protective agent for chlorine molecules, forming a complex that prevents them from breaking down due to sunlight exposure. This allows the chlorine to remain active and effective in sanitizing the pool water, reducing the need for frequent reapplication and ensuring a consistent level of sanitation.
However, it is important to use cyanuric acid trisodium salt in recommended concentrations, as overuse can lead to the buildup of cyanuric acid in pool water. This can reduce the effectiveness of chlorine and potentially pose health and environmental risks. Regular monitoring and maintenance of pool water chemistry are essential to ensure the safe and effective use of cyanuric acid trisodium salt as a stabilizer.

Check Digit Verification of cas no

The CAS Registry Mumber 3047-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3047-33:
(6*3)+(5*0)+(4*4)+(3*7)+(2*3)+(1*3)=64
64 % 10 = 4
So 3047-33-4 is a valid CAS Registry Number.
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

3047-33-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyanuric acid trisodium salt

1.2 Other means of identification

Product number -
Other names Na-cyanurate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. CBI
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3047-33-4 SDS

3047-33-4Relevant academic research and scientific papers

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

Kavina, M. A.,Sizov, V. V.

, p. 1046 - 1053 (2020)

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.

The Sodium (Iso)Cyanurates Nax[H3–xC3N3O3]·yH2O (x = 1–3, y = 0, 1): A Key-Series for Understanding the Crystal Chemistry of Metal (Iso)Cyanurates

Gross, Peter,H?ppe, Henning A.

, p. 257 - 266 (2019/02/03)

The (iso)cyanurates Na[H2C3N3O3]·H2O, Na2[HC3N3O3]·H2O, Na2[HC3N3O3], and Na3[C3N3O3] were synthesized phase pure from Na2CO3·10H2O, NaOH, and cyanuric acid, respectively, in aqueous solution by carefully adjusting the crystallization conditions. The crystal structures of all compounds were determined by single-crystal X-ray diffraction {Na2[HC3N3O3]·H2O: P1, a = 3.51660(10) ?, b = 7.8300(3) ?, c = 11.3966(4) ?, α = 86.4400(10)°, β = 85.5350(10)°, γ = 85.0720(10)°, Z = 2, R1 = 0.030, wR2 = 0.078; Na2[HC3N3O3]: Pnma, a = 6.3409(6) ?, b = 12.2382(13) ?, c = 6.5919(7) ?, Z = 4, R1 = 0.045, wR2 = 0.079; Na3[C3N3O3]: R3c, a = 11.7459(3) ?, c = 6.5286(3) ?, Z = 3, R1 = 0.039, wR2 = 0.066}. The structures show ribbons (Na[H2C3N3O3]·H2O), dimers (Na2[HC3N3O3]·H2O), chains (Na2[HC3N3O3]), or columns (Na3[C3N3O3]) of hydrogen-bonded and parallel stacked (iso)cyanurate anions. These motifs are shown to be characteristic for certain degrees of protonation and hydration, and all (iso)cyanurate crystal structures found so far were classified accordingly. X-ray powder patterns, thermogravimetry curves, IR and UV/Vis spectra were measured for all compounds.

Photosensitive resin composition for color filter and uses thereof

-

Page/Page column 33, (2017/03/08)

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.

LONG CHAIN ALKYLENE GROUP-CONTAINING EPOXY COMPOUND

-

, (2012/01/13)

It is an object to provide a liquid thermosetting composition that yields an epoxy resin having physical properties of the cured product such as high flexural strength along with adequate handleability as liquid, to be used in transparent sealants for optical semiconductors, such as transparent sealants for LEDs (light-emitting devices) and the like. There is provided a thermosetting composition containing an epoxy compound that a side chain between a triazinetrione ring and an epoxy group substituted on the triazinetrione ring is long (elongated).

HIGHLY CONCENTRATED BROMINE COMPOSITIONS AND METHODS OF PREPARATION

-

Page/Page column 67-71, (2008/06/13)

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.

Process for producing a metal phthalocyanine and/or its derivative

-

, (2008/06/13)

In a process for producing a metal phthalocyanine and/or its derivative by heating phthalic anhydride and/or its derivative, urea and a metal compound in an organic solvent in the presence of a catalyst, or by heating phthalodinitrile and a metal or a metal compound in an organic solvent, the improvement wherein the reaction for the production of the metal phthalocyanine and/or its derivative is conducted by an addition of cyanuric acid and/or its derivative.

Trisubstituted symmetrical triazines

-

, (2008/06/13)

Triazine derivatives of the formula: are described, wherein: R1, R2 and R3 are the same or different and represent a ring perhalogenated benzyl and/or xylylidene, and which are bonded to the triazine ring on the N atoms when the ring is saturated, or on the O atoms when the ring is unsaturated, and n is an integer between 1 and 5. The invention is further directed to flame-retardant compositions and to plastic compositions which comprise a compound of formula I.

Isocyanurate specific electrode and method of analysis and quaternary ammonium isocyanuric acid salts therefore

-

, (2008/06/13)

An electrode that is specific for the isocyanurate ion, and capable of rapid determination of the free isocyanurate ion activity directly in solution uses as its sensing element a platinum wire covered with a polyvinyl chloride membrane. The membrane is plasticized with a solution of a quaternary ammonium salt of isocyanuric acid. When this electrode and a commercial reference electrode are immersed in a solution containing the isocyanurate ion, a differential voltage proportional to the isocyanurate ion concentration is generated which is detected by a pH meter.

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