Sodium arsenite is a white or grayish-white powder or flakes.
Sodium arsenite is used as hide preservative, antiseptic, dyeing and soaps. It is used as a stressor to induce production of heat shock proteins.
Technical grade in manufacture of arsenical soap for use on skins, for treating vines against certain scale diseases; as insecticide especially for termites.
ChEBI: An inoganic sodium salt with formula with formula NaAsO2.
Sodium arsenite was historically produced through straightforward inorganic processing. Commercial manufacture followed the standard route for trivalent arsenite salts: reacting arsenious oxide with sodium hydroxide in controlled solution, adjusting stoichiometry to yield the meta arsenite form, and then concentrating and drying the product to a technical grade powder.
A white or grayish-white powder. Denser than water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation and skin absorption.
Soluble in water. Slowly converted in solution to arsenates by atmospheric oxygen; in dry state Sodium m-arsenite is decomposed by carbon dioxide. [EPA, 1998].
Salts, basic, such as SODIUM ARSENITE, are generally soluble in water. The resulting solutions contain moderate concentrations of hydroxide ions and have pH's greater than 7.0. They react as bases to neutralize acids. These neutralizations generate heat, but less or far less than is generated by neutralization of the bases in reactivity group 10 (Bases) and the neutralization of amines. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.
Toxic by ingestion and inhalation.
Extremely toxic: probable oral lethal dose (human) 5-50 mg/kg, between 7 drops and one teaspoon for 70 kg person (150 lb.). Poisonous if swallowed or inhaled. Human suspected carcinogen.
Sodium m-arsenite may burn but does not ignite readily. When heated Sodium m-arsenite emits toxic fumes of arsenic and sodium oxide. Slowly converted in solution to arsenates by atmospheric oxygen; in dry state Sodium m-arsenite is decomposed by carbon dioxide.
reaction type: Redox Reactions
Acts via enzyme inhibition
Confirmed human carcinogen. Human poison by ingestion. Experimental poison by ingestion, skin contact, intravenous, intramuscular, and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. Used as an herbicide and pesticide. When heated to decomposition it emits toxic fumes of arsenic and NazO. See also ARSENIC COMPOUNDS.
This material is used in manufacturing of arsenical soap for use on skin; treating vines against certain scale diseases; wood preservation; as a reagent in preparation of Methylene iodide; corrosion inhibitor; and for herbicidal and pesticidal purposes
UN2027 Sodium arsenite, solid, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN1686 Sodium arsenite, aqueous solutions, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
Chemically active metals. Arsine, a very deadly gas, can be released in the presence of acid, acid mists, or hydrogen gas.
The arsenic may be precipitated as calcium arsenite. It should be stored until recycled. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.
Herbicide; Insectiicde; Rodenticide; Fungicide
