CHLORIC ACID

CHLORIC ACID Basic information
Product Name:CHLORIC ACID
Synonyms:chloric;chloricacid;Hypure C;NA 2626;Chloric acid,aqueous solution,with not more than 10% chloric acid;Chloride Acid;CHLORIC ACID, 35 WT. % SOLUTION;NA-9191
CAS:7790-93-4
MF:ClHO3
MW:84.46
EINECS:232-233-0
Product Categories:Pharmaceutical Intermediates
Mol File:7790-93-4.mol
CHLORIC ACID Structure
CHLORIC ACID Chemical Properties
Melting point <-20℃ [CRC10]
Boiling point >100 °C
density 1.2 g/mL at 25 °C
Water Solubility very soluble H2O [CRC10]
Merck 13,2109
CAS DataBase Reference7790-93-4
EPA Substance Registry SystemChloric acid (7790-93-4)
Safety Information
Hazard Codes O,C
Risk Statements 8-34
Safety Statements 17-26-36/37/39-45
RIDADR 2626
HazardClass 5.1
PackingGroup II
MSDS Information
CHLORIC ACID Usage And Synthesis
DescriptionChloric 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


Chemical Propertiescan 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]
UsesOxidizing agent; with H2SO3 as catalyst in acrylonitrile polymerization.
DefinitionChEBI: Chloric acid is a chlorine oxoacid. It is a conjugate acid of a chlorate.
General DescriptionCHLORIC 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 ReactionsWater soluble.
Reactivity ProfileSelf-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.
HazardToxic by ingestion and inhalation. Strong oxidizer, ignites organic materials on contact.
Health HazardInhalation, 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 HazardThese 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 ProfileA 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.
CHLORIC ACID Preparation Products And Raw materials
Preparation ProductsHydrazine hydrate-->Sodium chlorate-->Crystal Violet-->Cyclopropylamine-->Cobalt oxide-->Estrone-->Disperse Red 60-->Moclobemide-->Butylnaphtalenesulfonic Acid Sodium Salt-->Sodium iodate-->CI 77492-->alkyl phenylsufonate-->sodium oleyl sarcosinate-->Starch, oxidized-->CHLORIDE STANDARD-->2-AMINO-4-CHLORO-6-NITROBENZOIC ACID
MERCURIC PERCHLORATE IRON(III) PERCHLORATE HYDRATE SILVER PERCHLORATE NICKEL(II) PERCHLORATE HEXAHYDRATE PERCHLORIC ACID Sodium perchlorate CRESYL VIOLET PERCHLORATE BARIUM PERCHLORATE Potassium perchlorate Sodium chlorate CESIUM PERCHLORATE Potassium chlorate BARIUM CHLORATE MONOHYDRATE ALUMINUM PERCHLORATE N-TERT-BUTYL-5-METHYLISOXAZOLIUM PERCHLORATE COPPER PERCHLORATE Lithium perchlorate Magnesium perchlorate

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