high quality Organic Intermediate Cyanuric Acid CAS 108-80-5 with best price

Cyanuric acid

1,3,5-Triazine-2,4,6(1H,3H,5H)-trione;Isocyanuric acid;s-Triazine-2,4,6(1H,3H,5H)-trione;Cyanuric acid;Tricyanic acid;Trihydroxycyanidine;2,4,6-Trihydroxy-1,3,5-triazine;s-Triazine-2,4,6-triol;Pseudocyanuric acid;2,4,6-Trihydroxy-s-triazine;2,4,6-Trioxohexahydro-1,3,5-triazine;5-Azabarbituric acid;ICA-P;1,3,5-Triazine-2,4,6-trione;NSC 6284;1,3,5-Triazine-2,4,6-triol;[1,3,5]Triazine-2,4,6-triol;134016-52-7;504-19-8;273203-07-9

108-80-5

C3H3N3O3

InChIKey=ZFSLODLOARCGLH-UHFFFAOYSA-N

129.07

129.07

126982

211-620-8

H497R4QKTZ

1313

6284

DTXSID7024873

White crystalline solid|CRYSTALLINE POWDER

29336980

Hydrazine or Hydroxylamine Derivatives

87.3

-1.2

White to light beige Crystalline Powder or Lumps

2.500 g/cm³ @ Temp: 20 °C

360 °C

155-158 °C

433.6±28.2 °C

1.4500 (estimate)

H2O: 0.3 g/100mL (25 ºC);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.

0-6°C

Vapour pressure, Pa at 25°C:

LD50 orally in rats: >5.00 g/kg (Canelli)

Odorless

Slightly bitter

pH of saturated aqueous solution @ room temperature = 4.8

Henry's Law constant = 8.74X10-15 atm-cu m/mol at 25 °C (est)

pKa1 = 6.88; pKa2 = 11.40; pKa3 = 13.5

SOL IN PYRIDINE; INSOL IN ACETIC ACID; MAX ABSORPTION (WATER PH= 8): 214 NM (LOG E= 4.01); DENSITY: 1.768 @ 0 °C; SADTLER REFERENCE NUMBER: 7027 (IR, PRISM) /DIHYDRATE/|1 MG/L= 189 PPM; 1 PPM= 5.28 MG/CU M; TENDS TO FORM SUPERSATURATED SOLUTIONS|Forms dihydrate in aqueous solution; crystalizes as colorless monoclinic prisms that efforesce in dry air. Predominant tautomeric form in solid state and solution is keto form, isocyanuric acid; in basic solutions the enol form is more stable.|Hydroxyl radical reaction rate constant = 3.0X10-12 cu cm/molec-sec at 25 °C (est)

Soluble in hot water [Hawley].

Amides and Imides

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)