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SODIUM FLUOROACETATE

Base Information Edit
  • Chemical Name:SODIUM FLUOROACETATE
  • CAS No.:62-74-8
  • Molecular Formula:C2H3 F O2 . Na
  • Molecular Weight:100.025
  • Hs Code.:29159000
  • Mol file:62-74-8.mol
SODIUM FLUOROACETATE

Synonyms:Aceticacid, fluoro-, sodium salt (8CI,9CI);1080;Compound 1080;Fluoroacetic acidsodium salt;Fratol;Furatol;Ratbane 1080;SMFA;Sodium fluoroacetate;Sodiummonofluoroacetate;Tenate;

Suppliers and Price of SODIUM FLUOROACETATE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • SodiumFluoroacetate
  • 25mg
  • $ 50.00
Total 1 raw suppliers
Chemical Property of SODIUM FLUOROACETATE Edit
Chemical Property:
  • Appearance/Colour:white odourless hygroscopic powder 
  • Vapor Pressure:0.828mmHg at 25°C 
  • Melting Point:200-205 °C (dec.)
     
  • Boiling Point:167.9°C at 760 mmHg 
  • PKA:2.66 
  • Flash Point:55.3°C 
  • PSA:40.13000 
  • LogP:-1.29420 
  • Water Solubility.:Very soluble 
Purity/Quality:

97% *data from raw suppliers

SodiumFluoroacetate *data from reagent suppliers

Safty Information:
  • Pictogram(s): Toxic by ingestion, inhalation, and skin absorption. TLV: 0.05 mg/m3; STEL 0.15 mg/m3. Toxic by skin absorption. For use by trained operators only, use has been restricted. 
  • Hazard Codes:T+,N,T 
  • Statements: 26/27/28-50 
  • Safety Statements: 13-22-36/37-45-61 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Description Sodium fluoroacetate is the salt of a naturally occurring toxin which is found in Australia, Brazil, and Africa. Naturally occurring fluoroacetate can be found in Gastrolobium minus (family: Fabaceae), a flowering plant in Western Australia and often referred to as the ‘poison pea.’ Descriptions of the fluoroacetate activity may have been described as early at 1904 in Sierra Leone, when colonists used extracts of Chailletia toxicaria to poison rats. The actions of fluoroacetate have also been described in animals having ingested the poison leaf Gifblaar (Dichapetalum cymosum). Sodium fluoroacetate was then developed as a rodenticide and predacide in 1942 in the United States and went under the synonym of 1080, which is its catalog number. In the late 1970s, the use of sodium fluoroacetate was significantly restricted in the United States due to its high acute toxicity and the need for specialized training for application. Additional restrictions were also imposed as to the locations that the agent could be used and under very defined conditions. A ‘toxic collar’ was developed which contains a very small amount of sodium fluoroacetate (0.3 mg per collar). This collar could be placed around the throats of livestock and would contain chemical pouches that would be ruptured when the animal was attacked by a predator thus restricting the poison only to the predator. The toxicity in certain predators (dogs, wolves, coyotes) is up to 20-fold higher than in humans. Amphibians and other reptiles have been shown to be relatively resistant to sodium fluoroacetate and can feed on insects and other animals which have high levels of sodium fluoroacetate present with no ill-effects. In the late 1980s, all use of sodium fluoroacetate as a rodenticide was discontinued. The availability of products containing sodium fluoroacetate is permitted by the Environmental Protection Agency (EPA) and the regulatory conclusion of the EPA is that these products will not pose unreasonable risks or adverse effects if the products are used following the restriction on the product labeling.
  • Uses Predator elimination (coyotes), rodenticide. Sodium fluoroacetate is used for rodent control in restricted environments and for the control of the brushtail possum and other wild mammals in some countries. Rodenticide (restricted use)
Technology Process of SODIUM FLUOROACETATE

There total 4 articles about SODIUM FLUOROACETATE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; In ethanol; at 0 ℃;
Guidance literature:
With sodium hydroxide; In tetrahydrofuran; for 2h; Reflux;
DOI:10.1021/acs.organomet.5b00369
Guidance literature:
In sodium hydroxide; at 100 ℃; for 3h; Kinetics;
DOI:10.1111/j.2042-7158.1998.tb06167.x
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