Cyanuric acid

ChemicalBook > CAS DataBase List > Cyanuric acid

Uses Methods of production

Product Name: Cyanuric acid
CAS No.: 108-80-5
Chemical Name: Cyanuric acid
Synonyms: ISOCYANURIC ACID;Triuret;1,3,5-TRIAZINE-2,4,6-TRIOL;Cyanuric acid-15N3;Lamotrigine Impurity 13;2,4,6-TRIHYDROXY-S-TRIAZINE;2,4,6-TRIHYDROXY-1,3,5-TRIAZINE;1,3,5-triazine-2,4,6(1h,3h,5h)-trione;cp4789;Zeonet A
CBNumber: CB5852763
Molecular Formula: C3H3N3O3
Formula Weight: 129.07
MOL File: 108-80-5.mol

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Cyanuric acid Property

Melting point:: 360 °C
Boiling point:: 74 °C
Density: 1.56
bulk density: 550kg/m3
vapor pressure: <0.0001 Pa (25 °C)
refractive index: 1.4500 (estimate)
storage temp.: Store below +30°C.
solubility: Soluble in sulfuric acid, dimethylformamide, sodium hydroxide, potassium hydroxide and diemthyl sulfoxide. Slightly soluble in acetone, benzene, diethyl ether, ethanol and hexane. Insoluble in cold methanol, benzene and chloroform.
form: Crystalline Powder or Lumps
pka: 6.88, 11.40, 13.5(at 25℃)
color: White to light beige
PH: 3.8-4.0 (H2O, 20℃)(saturated solution)
Odor: off-wh. cryst., odorless
Water Solubility: 0.3 g/100mL (25 ºC)
Merck: 14,2698
BRN: 126982
Stability:: Stable. Incompatible with strong oxidizing agents.
InChIKey: ZFSLODLOARCGLH-UHFFFAOYSA-N
LogP: -1.31 at 25℃
CAS DataBase Reference: 108-80-5(CAS DataBase Reference)
NIST Chemistry Reference: 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione(108-80-5)
EPA Substance Registry System: Cyanuric acid (108-80-5)

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Safety

Hazard Codes
HS Code: 29339900
Hazardous Substances Data: 108-80-5(Hazardous Substances Data)
Toxicity: LD50 orally in rats: >5.00 g/kg (Canelli)

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 8.20358
Product name: Cyanuric acid
Purity: for synthesis
Packaging: 5G
Price: $33.6
Updated: 2024/03/01

Sigma-Aldrich

Product number: 8.20358
Product name: Cyanuric acid
Purity: for synthesis
Packaging: 250g
Price: $35.5
Updated: 2024/03/01

Sigma-Aldrich

Product number: 8.20358
Product name: Cyanuric acid
Purity: for synthesis
Packaging: 1kg
Price: $98.4
Updated: 2024/03/01

Sigma-Aldrich

Product number: 8.20358
Product name: Cyanuric acid
Purity: for synthesis
Packaging: 50kg
Price: $713
Updated: 2024/03/01

Sigma-Aldrich

Product number: 185809
Product name: Cyanuric acid
Purity: 98%
Packaging: 25g
Price: $32.3
Updated: 2024/03/01

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Cyanuric acid Chemical Properties,Usage,Production

Uses

1.Used as ultraviolet absorbent for plastic film.
2.Used as chemical reagent, also used in organic synthesis.
3.Mainly used in the production of new bleaching agent, disinfectant, water treatment agent and resin, paint and metal cyanide corrosion inhibitor, etc.
4.Used for the synthesis of chloro derivatives, trichloroisocyanuric acid, dichloro isocyano uric acid sodium or potassium; used for synthesizing cyanuric acid-formaldehyde resin, epoxy resin, antioxidant, coatings, adhesives, pesticides, herbicides, metal cyanide inhibitor and polymer modifier; used in the manufacture of halotrizinol.

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.

Chemical Properties

white powder

Uses

Cyanuric acid is used in chemical synthesis (see Section 31.0), as an intermediate for chlorinated bleaches, as a selective herbicide, and as a whitening agent. The parent compound and salts, chlorinated salts, and chlorinated acids are used to disinfect swimming pools, restaurants, and barns. Chlorinated salts hydrolyze in water to form cyanurate and hypochlorous acid. Other monomeric isocyanurates (e.g., triallyl cyanurate) are used as cross-linking components for producing polyurethanes, polyesters, and alkyd resins. Tris (2-hydroxyethyl)isocyanurate is used in wire lacquers. Cyanuric acid is produced in the United States.

Uses

Diagnostic determination of Melamine and related compounds in kidney tissue.

Uses

Convenient lab source of cyanic acid gas. In preparation of melamine, sponge rubber, herbicides, dyes, resin, antimicrobial agents. As stabilizer and disinfectant in swimming pool water.

Definition

ChEBI: The keto tautomer of cyanuric acid.

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).

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.

General Description

Crystals.

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

Not classified

Purification Methods

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

Cyanuric acid Preparation Products And Raw materials

Raw materials

Urea Ammonium chloride Sulfuric acid

Preparation Products

TYCOR (TM) 1,3,5-Tri-2-propenyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione Chloroacetone Trichloroisocyanuric acid DICHLOROISOCYANURIC ACID Metribuzin Antioxidant3114 1,3,5-Triglycidyl isocyanurate 1,3-Dichloro-1,3,5-triazinetrione,sodium salt Sodium dichloroisocyanurate 1,3,5-Tris(2-hydroxyethyl)cyanuric acid

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View Lastest Price from Cyanuric acid manufacturers

Hebei Mujin Biotechnology Co.,Ltd

Product: Cyanuric acid 108-80-5
Price: US $0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 50000KG/month
Release date: 2023-06-21

Hebei Zhuanglai Chemical Trading Co.,Ltd

Product: Cyanuric Acid 108-80-5
Price: US $120.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 20ton
Release date: 2024-05-14

Jinan Finer Chemical Co., Ltd

Product: Cyanuric acid 108-80-5
Price: US $0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 5000mt
Release date: 2022-06-17

108-80-5, Cyanuric acidRelated Search:

Chrysin Ethyl 2-(Chlorosulfonyl)acetate Trifluoperazine Hyaluronic acid Citric acid 1,3,5-Triazine DICHLOROISOCYANURIC ACID Trichloroisocyanuric acid Lamotrigine ALMITRINE Melamine cyanurate Folic acid Sodium dichloroisocyanurate Cyanuric chloride 2-Amino-4-methoxy-6-methyl-1,3,5-triazine Ceftriaxone sodium 2-Pyrrolidinecarbonitrile,1-acetyl-,(2S)-(9CI) Dichloroacetyl chloride

2,4,6-Triazinetrione

2,4,6-Trihydroxytriazine

1,3,5-triazine-2,4,6(1h,3h,5h)-trione

-Azabarbituric acid

cp4789

Cyanuric acid, anhydride

cyanuricacid(non-specificname)

Cyanursαure

Isocyanurate acid

Kyselina kyanurova

Triuret

Zeonet A

SYM-TRIAZINETRIOL

1,3,5-TRIAZINE-2,4,6-TRIOL

1,3,5-TRIAZINE-2,4,6-TRIONE

2,4,6-TRIHYDROXY-1,3,5-TRIAZINE

2,4,6-TRIHYDROXY-S-TRIAZINE

ISOCYANURIC ACID

CYANURIC ACID

cyanuric acid anhydrous

Fulminuric acid

Cyanuric acid(CA)

Cyanuric Acid (1.0 Mg/10 ML in 84:16% ACN:H2O)

Cyanuric acid 98%

Cyanuric acid-15N3

Gimeracil Impurity 4

Cyanauric Acid

Vildagliptin Impurity 26

2,4,6-Tricyanic acid

CYANURIC ACID, 98%CYANURIC ACID, 98%CYANURIC ACID, 98%CYANURIC ACID, 98%

Lamotrigine Impurity 13

2-cyano-2-nitroethanamide

cyanonitroacetamide

Tricyanide

trihydroxytriazine

TRICARBIMIDE

TRICYANIC ACID

trihydroxy-1,3,5-triazine

Trihydroxycyanidine

,4,6-Trihydroxy-S-triazine

,4,6-Trioxohexahydro-1,3,5-triazine

[1,3,5]triazinane-2,4,6-trione

[1,3,5]Triazintrion

1,3,5-Triazine-2,4,6-(1H,3H,5H)triol

1,3,5-Triazine-2,4,6-(1H,3H,5H)-trion

kyselinakyanurova

kyselinakyanurova(czech)

Normalcyanuricacid

Pseudocyanuric acid

pseudocyanuricacid

s-2,4,6-Triazinetriol

s-Triazine-2,4,6(1H,3H,5H)-trione

s-Triazine-2,4,6-triol

s-Triazine-2,4,6-trione

s-Triazinetriol

s-Triazinetrione

ISOCYANURIC ACID (ICA)

1,3,5-TRIAZINO-2,4,6-TRIOL