| Description | Chloric acid, HClO3, is an oxoacid of chloride, andthe formal precursor of chlorate salts. It is a strongacid (pKa＝-1) and a strong oxidizing agent. It is stablein cold aqueous solution up to a concentration ofapproximately 30%, and solution of up to 40% can beprepared by careful evaporation under reduced pressure.Above these concentrations, and on warming,chloric acid solutions decompose to give a variety ofproducts, for example:
8HClO3→4HClO4＋2H2O＋2Cl2＋3O2
Note that it disproportionates into perchloric acidin which the chlorine atom has a＋7 oxidation stateand also the zero oxidation state of chlorine gas (anoxidation–reduction reaction). Thus, under the properconditions, it can also be used to make perchloric acid.
3HClO3→HClO4＋H2O＋2ClO2 |
| Chemical Properties | can occur only in an aqueous solution; oxidizing agent; preparation: reaction between H2SO4 and barium chlorate; used as a catalyst in the polymerization of acrylonitrile, as an oxidizing agent [MER06] [HAW93] |
| Uses | Oxidizing agent; with H2SO3 as catalyst in acrylonitrile polymerization. |
| Definition | ChEBI: Chloric acid is a chlorine oxoacid. It is a conjugate acid of a chlorate. |
| General Description | CHLORIC ACID is a colorless liquid. CHLORIC ACID will accelerate the burning of combustible materials and can ignite most on contact. CHLORIC ACID is corrosive to metals and tissue. CHLORIC ACID is used as a reagent in chemical analysis and to make other chemicals. |
| Air & Water Reactions | Water soluble. |
| Reactivity Profile | Self-reactive. Concentrations of CHLORIC ACID above 40% decompose [Mellor 2 Supp. 1:576 1956]. Antimony sulfide and concentrated solutions of CHLORIC ACID react with incandescence [Mellor Supp. II Part I:584 1956]. Arsenic sulfide and concentrated solutions of CHLORIC ACID react with incandescence . Reacts with vigor even explodes with other metal sulfides, i.e. copper sulfide [Mellor Supp. II Part I:584 1956]. In contact with oxidizable materials, including ammonia, reactions can be extremely violent. Filter paper ignites after soaking in CHLORIC ACID, [Mellor, 1946, Vol. 2, 310]. Explosions have been recorded by mixtures of CHLORIC ACID solution with metals such as: antimony, bismuth, and iron. This is due to the formation of explosive compounds including hydrogen. |
| Hazard | Toxic by ingestion and inhalation. Strongoxidizer, ignites organic materials on contact. |
| Health Hazard | Inhalation, ingestion or contact (skin, eyes) with vapors or substance may cause severe injury, burns or death. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution. |
| Fire Hazard | These substances will accelerate burning when involved in a fire. Some may decompose explosively when heated or involved in a fire. May explode from heat or contamination. Some will react explosively with hydrocarbons (fuels). May ignite combustibles (wood, paper, oil, clothing, etc.). Containers may explode when heated. Runoff may create fire or explosion hazard. |
| Safety Profile | A poison. A strong irritant by ingestion and inhalation. Dangerous fire hazard; ignites organic matter upon contact. A very powerful oxidizing agent. Violent or explosive reaction with oxidlzable materials. Aqueous solutions decompose explosively during evaporation. Solutions greater than 40% are unstable. Reacts violently with NH3, Sb, Sb2S3, AsS3， Bi, CuS, PHI4+ SnS2, SnS. Reaction with cellulose causes ignition after a delay period. Dangerous reaction with metal sulfides and metal chlorides (e.g., incandescent reaction with antimony trisulfide, arsenic trisulfide, tin(lI)sulfide, tin(Iv> sulfide, explosion on contact with copper sulfide). Reaction with metals (e.g., antimony, bismuth, iron) forms explosive products. When heated to decomposition it emits toxic fumes of Cl-. See also CHLORATES and CHLORINE. |
