Difference between revisions of "Cyanuric acid"

From Sciencemadness Wiki
Jump to: navigation, search
 
(4 intermediate revisions by 2 users not shown)
Line 1: Line 1:
 
{{Chembox
 
{{Chembox
| Name =Cyanuric acid
+
| Name = Cyanuric acid
 
| Reference =
 
| Reference =
| IUPACName =1,3,5-Triazinane-2,4,6-trione
+
| IUPACName = 1,3,5-Triazinane-2,4,6-trione
 
| PIN =
 
| PIN =
 
| SystematicName =
 
| SystematicName =
 
| OtherNames = 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione<br>1,3,5-Triazinetriol<br>s-Triazinetriol<br>s-Triazinetrione<br>Tricarbimide<br>Isocyanuric acid<br>Pseudocyanuric acid
 
| OtherNames = 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione<br>1,3,5-Triazinetriol<br>s-Triazinetriol<br>s-Triazinetrione<br>Tricarbimide<br>Isocyanuric acid<br>Pseudocyanuric acid
 
<!-- Images -->
 
<!-- Images -->
| ImageFile =  
+
| ImageFile = Cyanuric_acid.jpg
| ImageSize =  
+
| ImageSize = 270
 
| ImageAlt =  
 
| ImageAlt =  
 
| ImageName =  
 
| ImageName =  
Line 67: Line 67:
 
| SolubleOther = Soluble in [[Dimethyl sulfoxide|DMSO]], conc. [[hydrochloric acid|HCl]], [[pyridine]], conc. [[sulfuric acid]]<br>Slightly soluble in [[Dimethylformamide|DMF]], [[ethanol]]<br>Insoluble in [[acetone]], [[benzene]], [[chloroform]], [[diethyl ether]], [[methanol]]
 
| SolubleOther = Soluble in [[Dimethyl sulfoxide|DMSO]], conc. [[hydrochloric acid|HCl]], [[pyridine]], conc. [[sulfuric acid]]<br>Slightly soluble in [[Dimethylformamide|DMF]], [[ethanol]]<br>Insoluble in [[acetone]], [[benzene]], [[chloroform]], [[diethyl ether]], [[methanol]]
 
| Solvent =  
 
| Solvent =  
| VaporPressure = 4.41·10<sup>-11</sup> mmHg at 25 °C
+
| VaporPressure = 4.41·10<sup>-11</sup> mmHg (25 °C)
 
   }}
 
   }}
 
| Section3 = {{Chembox Structure
 
| Section3 = {{Chembox Structure
Line 121: Line 121:
  
 
==Preparation==
 
==Preparation==
Can be prepared by thermal decomposition of [[urea]]. However, it's much cheaper to simply buy the compound.
+
Can be prepared by thermal decomposition of [[urea]]. It is also created when generating chlorine from [[TCCA]] and [[hydrochloric acid]], which is rather impractical for the preparation of cyanuric acid because of the large amounts of chlorine being produced. Rather, it's much cheaper to simply buy the compound.
  
 
==Projects==
 
==Projects==
Line 136: Line 136:
 
===Disposal===
 
===Disposal===
 
No special disposal is required, can be poured down the drain in the trash.
 
No special disposal is required, can be poured down the drain in the trash.
 +
 +
==Gallery==
 +
<gallery widths="200" position="center" columns="4" orientation="none">
 +
Calcium_cyanurate.jpg|Calcium cyanurate made by the method of AllChemystery
 +
</gallery>
  
 
==References==
 
==References==
Line 150: Line 155:
 
[[Category:Readily available chemicals]]
 
[[Category:Readily available chemicals]]
 
[[Category:Triazines]]
 
[[Category:Triazines]]
 +
[[Category:Essential reagents]]

Latest revision as of 15:18, 18 November 2023

Cyanuric acid
Cyanuric acid.jpg
Names
IUPAC name
1,3,5-Triazinane-2,4,6-trione
Other names
1,3,5-Triazine-2,4,6(1H,3H,5H)-trione
1,3,5-Triazinetriol
s-Triazinetriol
s-Triazinetrione
Tricarbimide
Isocyanuric acid
Pseudocyanuric acid
Properties
C3H3N3O3
Molar mass 129.07 g/mol
Appearance White solid
Odor Odorless
Density 2.5 g/cm3
Melting point 320–360 °C (608–680 °F; 593–633 K) (decomposes)
Boiling point Decomposes
0.27 g/100 ml (25 °C)
Solubility Soluble in DMSO, conc. HCl, pyridine, conc. sulfuric acid
Slightly soluble in DMF, ethanol
Insoluble in acetone, benzene, chloroform, diethyl ether, methanol
Vapor pressure 4.41·10-11 mmHg (25 °C)
Hazards
Safety data sheet Sigma-Aldrich
Lethal dose or concentration (LD, LC):
7,700 mg/kg (rat, oral)
5,000 mg/kg (rabbit, dermal)
Related compounds
Related compounds
Trichloroisocyanuric acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Cyanuric acid (or 1,3,5-triazine-2,4,6-triol) is a chemical compound with the formula (CNOH)3, often encountered as as bleach.

Properties

Chemical

Thermal decomposition of cyanuric acid in the presence of an alkali base yields cyanates and carbon oxides.

Physical

Cyanuric acid is an odorless white solid, poorly soluble in water.

Availability

Cyanuric acid is available as chlorine stabilizer in swimming pools and can be purchased from hardware stores.

Preparation

Can be prepared by thermal decomposition of urea. It is also created when generating chlorine from TCCA and hydrochloric acid, which is rather impractical for the preparation of cyanuric acid because of the large amounts of chlorine being produced. Rather, it's much cheaper to simply buy the compound.

Projects

Handling

Safety

Cyanuric acid has low toxicity, though it may be slightly irritant.

Storage

Cyanuric acid should be kept in closed bottles.

Disposal

No special disposal is required, can be poured down the drain in the trash.

Gallery

References

Relevant Sciencemadness threads