Chloric acid, HClO3, is an oxoacid of chloride, and
the formal precursor of chlorate salts. It is a strong
acid (pKa＝-1) and a strong oxidizing agent. It is stable
in cold aqueous solution up to a concentration of
approximately 30%, and solution of up to 40% can be
prepared by careful evaporation under reduced pressure.
Above these concentrations, and on warming,
chloric acid solutions decompose to give a variety of
products, for example:
8HClO3→4HClO4＋2H2O＋2Cl2＋3O2
Note that it disproportionates into perchloric acid
in which the chlorine atom has a＋7 oxidation state
and also the zero oxidation state of chlorine gas (an
oxidation–reduction reaction). Thus, under the proper
conditions, it can also be used to make perchloric acid.
3HClO3→HClO4＋H2O＋2ClO2
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]
Oxidizing agent; with H2SO3 as catalyst in acrylonitrile polymerization.
ChEBI: Chloric acid is a chlorine oxoacid. It is a conjugate acid of a chlorate.
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.
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.
Toxic by ingestion and inhalation. Strong
oxidizer, ignites organic materials on contact.
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.
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.
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.
