Cyanuric acid

Basic information

  • Product Name:Cyanuric acid
  • CasNo.:108-80-5
  • MF:C3H3N3O3
  • MW:129.075

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:360 °C
  • Packing:white powder
  • Throughput:
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Product Details

CasNo: 108-80-5

MF: C3H3N3O3

Appearance: white powder

Manufacturer Sells Best Quality Cyanuric acid 108-80-5 with stock

  • Molecular Formula:C3H3N3O3
  • Molecular Weight:129.075
  • Appearance/Colour:white powder 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:360 °C 
  • Refractive Index:1.748 
  • Boiling Point:793.4 °C at 760 mmHg 
  • PKA:6.88, 11.40, 13.5(at 25℃) 
  • Flash Point:433.6 °C 
  • PSA:98.58000 
  • Density:2.500 g/cm3 
  • LogP:-2.24850 

Cyanuric acid(Cas 108-80-5) Usage

Methods of production

It is obtained by the polymerization of urea. Mixed urea and ammonium chloride, heating and melting, stirring and temperature to 210℃, solution thickened, warming up to 230℃, melting gradually solidified, stir fry evenly, continue to heat up to 250℃, thermal insulation for 15 min, cold to 100℃, adding a small amount of water immersion and down to room temperature in water soaking crushed, filtered solids. The water and hydrochloric acid are added into the solid, stirring and heating to 110 ℃, insulation for 3 h, supplementing with hydrochloric acid and water, cooling to 30 ℃, and washing to neutral, filter, filter cake with water washing and drying to obtain the product. The product purity is ≥95%, consumption of urea 1200kg per ton of product.

Production Methods

Cyanuric acid is an odorless, crystalline powder. Chlorinated isocyanuratesareusuallypreparedbycontrolledchlorinationof the sodium or potassium salts of cyanuric acid. Other monomeric isocyanurates made from the parent compound include tris(2-hydroxyethyl)isocyanurate and triallyl cyanurate.

Air & Water Reactions

Soluble in hot water [Hawley].

Reactivity Profile

An amide and amine. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generate mixed oxides of nitrogen (NOx)

Flammability and Explosibility

Notclassified

Purification Methods

It crystallises from water. Dry it at room temperature in a desiccator in a vacuum. [Beilstein 26 III/IV 632.]

Definition

cyanuric acid: A white crystallinewater-soluble trimer of cyanic acid,(HNCO)3. It is a cyclic compound havinga six-membered ring made of alternatingimide (NH) and carbonyl(CO) groups (i.e. three -NH-C(O)-units). It can also exist in a phenolicform (three -N=C(OH)- units).

General Description

Crystals.

InChI:InChI=1/C3H3N3O3/c7-1-2(8)4-6-5-3(1)9/h(H,6,7)(H2,4,5,8,9)

108-80-5 Relevant articles

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Kitawaki,Sugino

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An All-Organic D-A System for Visible-Light-Driven Overall Water Splitting

Di, Jun,Lei, Yucheng,Li, Huaming,Liu, Chuntai,Liu, Daobin,Lv, Chade,Mo, Zhao,Song, Yanhua,Xu, Hui,Yan, Pengcheng,Yan, Qingyu,Yu, Qing,Zhu, Xingwang

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Direct water splitting over photocatalys...

A proof of the direct hole transfer in photocatalysis: The case of melamine

Maurino, Valter,Minella, Marco,Sordello, Fabrizio,Minero, Claudio

, p. 57 - 67 (2016)

The photoinduced transformation of 2,4,6...

An HPLC method with UV detection, pH control, and reductive ascorbic acid for cyanuric acid analysis in water

Cantu,Evans,Kawahara,Shoemaker,Dufour

, p. 5820 - 5828 (2000)

Every year over 250 million pounds of cy...

Reactions of hydrated electrons with triazine derivatives in aqueous medium

Varghese, Rani,Mohan, Hari,Manoj,Manoj,Aravind, Usha K.,Vandana,Aravindakumar

, p. 8171 - 8176 (2006)

A study is made of the kinetics and mech...

Synthese und Reaktionen von O-Cyano-acetonoxim

Kristinsson, Haukur,Winkler, Tammo

, p. 970 - 972 (1982)

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Kurzer

, p. 1258,1261 (1951)

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Smolka,Friedreich

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Photocatalytic degradation of the herbicide terbuthylazine: Preparation, characterization and photoactivity of the immobilized thin layer of TiO2/chitosan

Le Cunff, Jér?me,Toma?i?, Vesna,Wittine, Ozren

, p. 22 - 29 (2015)

The aim of this study was to immobilize ...

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Grundmann,Beyer

, p. 1948 (1954)

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Cyanuric and thiocyanuric esters as carriers of boron-containing fragments and their fragmentation in mass spectrometry

Azev, Yuri A.,Dülcks, Thomas,Gabel, Detlef

, p. 8689 - 8691 (2003)

Tripropargylic esters 2 and 10 of cyanur...

Synthesis and cytotoxic activity of trisubstituted-1,3,5-triazines

Arya, Kapil,Dandia, Anshu

, p. 3298 - 3304 (2007)

1,3,5-Triazine derivatives were screened...

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Werner, E. A.,Fearon, W. R.

, p. 1356 - 1362 (1920)

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Synthesis of pyrimidines and triazines in ice: Implications for the prebiotic chemistry of nucleobases

Menor-Salvan, Cesar,Ruiz-Bermejo, Dra. Marta,Guzman, Marcelo I.,Osuna-Esteban, Susana,Veintemillas-Verdaguer, Sabino

, p. 4411 - 4418 (2009)

Herein, we report the efficient synthesi...

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Venable,Moore

, p. 1750 (1917)

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Oxidation of atrazine by photoactivated potassium persulfate in aqueous solutions

Khandarkhaeva,Aseev,Sizykh,Batoeva

, (2016)

General laws of the photochemical oxidat...

Using bar infrared spectra and coincidence indexes to study the diversity of solid cyanuric acid structures

Nilo, Marcela C. B. G.,Sim?es, Thais G.,Neto, Claudio Costa

, p. 1499 - 1515 (2018)

A general method was developed for study...

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Eley et al.

, (1973)

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Moore,Thomas

, p. 1120 (1918)

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Degradation of melamine in aqueous systems by vacuum UV-(VUV-) photolysis. An alternative to photocatalysis

Bianco Prevot, Alessandra,Maurino, Valter,Fabbri, Debora,Braun, André M.,Gonzalez, Mónica C.

, p. 286 - 293 (2020)

VUV-irradiation experiments with aqueous...

HYDROLYTIC CONVERSIONS OF 2,4-DIAZIDO-6-ALKOXY-s-TRIAZINES

Azev, Yu. A.,Loginova, I. P.,Golomolzin, B. V.,Mudretsova, I. I.,Rusinov, V. L.

, p. 118 - 119 (1990)

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Walters,Wise

, p. 2472 (1917)

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Liquid-phase synthesis of cyanuric acid from urea

She, Dong-Mei,Yu, Hai-Lin,Huang, Qi-Liang,Li, Fen-Ming,Li, Chun-Jiu

, p. 1898 - 1902 (2010)

The focus of this paper was to identify ...

Phosphorus-Doped Carbon Nitride Tubes with a Layered Micro-nanostructure for Enhanced Visible-Light Photocatalytic Hydrogen Evolution

Guo, Shien,Deng, Zhaopeng,Li, Mingxia,Jiang, Baojiang,Tian, Chungui,Pan, Qingjiang,Fu, Honggang

, p. 1830 - 1834 (2016)

Phosphorus-doped hexagonal tubular carbo...

Novel one-dimensional polymeric Cu(II) complexes via Cu(II)-assisted hydrolysis of the 2,4-bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-methoxy-1,3,5-triazine pincer ligand: Synthesis, structure, and antimicrobial activities

Soliman, Saied M.,El-Faham, Ayman,El Silk, Sobhy E.

, (2020)

Two unexpected one-dimensional coordinat...

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Zobrist,Schinz

, p. 2380,2385 (1952)

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A new three-step procedure for the synthesis of cyanuric acid from urea

Lebedev,Sheludyakov,Lebedeva

, p. 793 - 795 (2014)

A new procedure for preparing high-purit...

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Curtius,Sieber

, p. 445,448,449,450 (1930)

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Photocatalytic removal of s-triazines: Evaluation of operational parameters

López-Mu?oz,Aguado,Revilla

, p. 153 - 162 (2011)

The photocatalytic degradation of atrazi...

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Senier,Walsh

, p. 290 (1902)

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Herzig

, p. 398 (1881)

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, p. 1051 (1955)

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Addition of 2-(3,5-dimethyl-1H-pyrazol-1-yl)ethanamine to methyl acrylate and cyclization of the adducts

Hayotsyan,Khachatryan,Badalyan,Attaryan,Hasratyan

, p. 193 - 195 (2016)

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Preparation of diselenides by the oxidation of selenols using trichloroisocyanuric acid

Zhong,Guo

, p. 1507 - 1510 (2001)

Selenols are readily oxidized to diselen...

Microwave assisted pyrolysis of urea supported on graphite under solvent-free conditions

Chemat, Farid,Poux, Martine

, p. 3693 - 3695 (2001)

The coupling of graphite (support) with ...

Machine-Learning-Assisted Selective Synthesis of a Semiconductive Silver Thiolate Coordination Polymer with Segregated Paths for Holes and Electrons

Inokuchi, Akihiro,Kamakura, Yoshinobu,Nishikubo, Ryosuke,Ogasawara, Kazuyoshi,Saeki, Akinori,Shibahara, Hiroki,Tanaka, Daisuke,Wakiya, Takuma,Yoshikawa, Hirofumi

, p. 23217 - 23224 (2021)

Coordination polymers (CPs) with infinit...

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Bann,Miller

, p. 131 (1958)

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THE PROCESS FOR OBTAINING OF FLUORALKYLATED CARBON QUANTUM DOTS

-

, (2022/02/27)

The invention discloses a simple, scalab...

108-80-5 Process route

bromine
7726-95-6

bromine

urea
57-13-6

urea

cyanuric acid
108-80-5,27026-93-3,27941-25-9

cyanuric acid

ammonium bromide

ammonium bromide

nitrogen
7727-37-9

nitrogen

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

Conditions
Conditions Yield
hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

2,4,6-tris(4-nitrophenoxy)-1,3,5-triazine
1919-18-2

2,4,6-tris(4-nitrophenoxy)-1,3,5-triazine

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

isocyanuric acid
108-80-5

isocyanuric acid

Conditions
Conditions Yield

108-80-5 Upstream products

  • 75-44-5
    75-44-5

    phosgene

  • 108-77-0
    108-77-0

    1,3,5-trichloro-2,4,6-triazine

  • 14921-00-7
    14921-00-7

    cyanuric bromide

  • 108-78-1
    108-78-1

    2,4,6-triamino-s-triazine

108-80-5 Downstream products

  • 420-05-3
    420-05-3

    cyanic acid

  • 590-28-3
    590-28-3

    potassium cyanate

  • 17497-85-7
    17497-85-7

    1,3,5-tribromo-1,3,5-triazinane-2,4,6-trione

  • 87-90-1
    87-90-1

    trichloroisocyanuric acid