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Natriumfluoracetat

Sodium Fluoroacetate

HCID 16212360
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Grundinformationen

CAS
62-74-8
Standard-SMILES
O=C([O-])CF.[Na+]
InChIKey
JGFYQVQAXANWJU-UHFFFAOYSA-M
Summenformel
C2H2FO2.Na
Durchschnittliche Molmasse
100,02 g/mol
Monoisotopische Masse
99,9936518

Überblick

Sodium Fluoroacetate can cause male reproductive toxicity according to The Environmental Protection Agency (EPA).

Namen und Bezeichner

Bevorzugter Name
Sodium Fluoroacetate
IUPAC
sodium 2-fluoroacetate
Lokaler Name
Natriumfluoracetat
Englischer Name
Sodium fluoroacetate
Summenformel
C2H2FNaO2
Molmasse
100.02

Namen und Synonyme

sodium fluoroacetate62-74-8Sodium monofluoroacetateCompound 1080YasoknockFratolFuratolTenateNatriumfluoracetatFluorakil 3Sodium fluoacetateSodium fluoracetate
Weitere Namen anzeigen
sodium 2-fluoroacetate1080smfatl869Na2AsHO4compd1080latka1080
Sodium fluoacetic acidRatbane 1080Fluoroctan sodnyFluoroacetic acid sodium saltNatriumfluoracetaatRCRA waste number P058Fluoroacetate de sodiumFluoroacetic acid, sodium salt

Datenbank-Bezeichner

CAS
62-74-8、62-74-7
PubChem CID
16212360
DTXSID
DTXSID8024311
ChEMBL
CHEMBL369611
ChEBI
CHEBI:38699
UNII
166WTM3843
EC Number
200-548-2
Nikkaji
J2.353A

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

Polarare Oberfläche (TPSA)
40,1 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
1
Schwere Atome
6
Formalladung
0
Komplexität
46,8

Experimentelle und physikochemische Eigenschaften

Pesticides · 2 Einträge

Pesticide -> EPA IRIS

Pesticides -> Rodenticides

OdorOdorless
Density · 2 Einträge

greater than 1 (temperature not listed) (USCG, 1999)

>1

Color/Form · 4 Einträge

White solid

Fluffy, colorless to white (sometimes dyed black) powder [Note: A liquid above 95 degrees F]

Colorless powder

Fine, white powder or monoclinic crystals

Solubility · 6 Einträge

Miscible (NIOSH, 2024)

Solubility (g/100 g) at 25 °C in: water: 111

Almost insoluble in ethanol, acetone, and petroleum oils

Solubility (g/100 g) at 25 °C in: methanol: 5; ethanol: 1.4; acetone: 0.04; carbon tetrachloride: 0.004

Practically insoluble in MeCO3

Solubility in water: good

Boiling Point · 3 Einträge

Decomposes (NIOSH, 2024)

decomposes

Decomposes

Decomposition · 4 Einträge

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H300: Fatal if swallowed [Danger Acute toxicity, oral]

P260, P262, P264, P270, P271, P273, P280, P284, P301+P316, P302+P352, P304+P340, P316, P320, P321, P330, P361+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Danger

H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]

P260, P262, P264, P270, P271, P273, P280, P284, P301+P316, P302+P352, P304+P340, P316, P320, P321, P330, P361+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 3 Einträge

Hazard Traits - Reproductive Toxicity

Sodium fluoroacetate (1080): HSNO Approval: HSR002771 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Acetic acid, fluoro-, sodium salt: Environment tier I assessment
DOT LabelPoison
Fire Hazards · 3 Einträge

When heated to decomposition, it emits highly toxic fumes of sodium oxide and fluorides. Avoid decomposing heat. (EPA, 1998)

· Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes.

Not combustible. Gives off irritating or toxic fumes (or gases) in a fire.

Fire PotentialNot flammable or combustible.
Health Hazards · 2 Einträge

Chemie und Industrie

Pharmakologische Informationen

Mechanism of Action · 5 Einträge

Sodium fluoroacetate (SFAC) or Compound 1080 is a potent rodenticide, largely used after 1946 for rodent and home pest control. The toxic effects of SFAC are caused by fluorocitrate action, a toxic metabolite, which has a competitive action with aconitase enzyme, leading to citrate accumulation and resulting in interference in energy production by Krebs cycle blockade. ...

Sodium monofluoroacetate (1080) is a vertebrate pesticide widely used for possum control in New Zealand. Fluoroacetate is also a toxic component of poisonous plants found in Australia, South Africa, South America, and India. Because of its importance and effectiveness in pest control and the highly toxic nature of this compound, its acute sub-lethal and target organ toxicity have been extensively studied. In relation to its use as a pesticide its environmental fate, persistence, non-target impacts and general toxicology have been and continue to be extensively studied. Toxic baits must be prepared and used with extreme care, otherwise humans, livestock, and non-target wildlife will be put at risk. The high risk of secondary poisoning of dogs is a cause for concern. 1080 acts by interfering with cellular energy production. Possums die from heart failure, usually within 6-18 hr of eating baits. Long-term exposure to sub-lethal doses can have harmful effects and strict safety precautions are enforced to protect contractors and workers in the bait manufacturing industry. Considerable care is taken when using 1080 to ensure that the risks of using it are outweighed by the ecological benefits achieved from its use. When its use is controversial, risk communicators must take care not to trivialize the toxicity of the compound. The benefits of 1080 use in conservation, pest control, and disease control should be weighed up alongside the risks of using 1080 and other techniques for pest control.

Active neurons have a high demand for energy substrate, which is thought to be mainly supplied as lactate by astrocytes. Heavy lactate dependence of neuronal activity suggests that there may be a mechanism that detects and controls lactate levels and/or gates brain activation accordingly. Here, we demonstrate that orexin neurons can behave as such lactate sensors. Using acute brain slice preparations and patch-clamp techniques, we show that the monocarboxylate transporter blocker alpha-cyano-4-hydroxycinnamate (4-CIN) inhibits the spontaneous activity of orexin neurons despite the presence of extracellular glucose. Furthermore, fluoroacetate, a glial toxin, inhibits orexin neurons in the presence of glucose but not lactate. Thus, orexin neurons specifically use astrocyte-derived lactate. The effect of lactate on firing activity is concentration dependent, an essential characteristic of lactate sensors. Furthermore, lactate disinhibits and sensitizes these neurons for subsequent excitation. 4-CIN has no effect on the activity of some arcuate neurons, indicating that lactate dependency is not universal. Orexin neurons show an indirect concentration-dependent sensitivity to glucose below 1 mm, responding by hyperpolarization, which is mediated by ATP-sensitive potassium channels composed of Kir6.1 and SUR1 subunits. In conclusion, our study suggests that lactate is a critical energy substrate and a regulator of the orexin system. Together with the known effects of orexins in inducing arousal, food intake, and hepatic glucose production, as well as lactate release from astrocytes in response to neuronal activity, our study suggests that orexin neurons play an integral part in balancing brain activity and energy supply.

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Decomp when heated above melting point.

Decomp at 200 °C

When heated to decomposition it emits highly toxic fumes of /sodium oxide and hydrogen flouride/

200 °C

Melting Point · 5 Einträge

392 °F Decomposes at 392 °F. (EPA, 1998)

200-202 °C; decomposes above melting point

392 °F (decomposes)

200 °C

392 °F

Vapor Pressure · 5 Einträge

0 mmHg at 68 °F (EPA, 1998)

VP: Non-volatile

Approx 0.0 mm Hg at 20 °C

low

Low

Physical Description · 5 Einträge

Sodium fluoroacetate appears as a fine, white, odorless, powdered solid. Toxic by ingestion, inhalation and skin absorption. Used as a rodenticide.

Fluffy, colorless to white (sometimes dyed black), odorless powder. [Note: A liquid above 95 degrees F.] [rodenticide] [NIOSH]

COLOURLESS SOLID IN VARIOUS FORMS.

Fluffy, colorless to white (sometimes dyed black), odorless powder.

Fluffy, colorless to white (sometimes dyed black), odorless powder. [Note: A liquid above 95 °F.] [rodenticide]

Stability/Shelf LifeNon-volatile
Dissociation ConstantspKa = 2.72 at 25 °C

Physikochemische Eigenschaften

Schmelzpunkt
200 · 200-205 °C (dec.)
Siedepunkt
105 · 105-106 °C
Dampfdruck
Non-volatile
Löslichkeit
DMSO (Sparingly), Methanol (Slightly)
Aggregatzustand
Fine white powder
pka
2.66 · 2.66
Wasserlöslichkeit
Very soluble
Merck
13 · 13,4194
Stabilität
Stable. Flammable. Risk of explosion above flashpoint.
CAS Datenbank
62 · 62-74-8(CAS DataBase Reference)
EPA chemische Informationen
Sodium fluoroacetate (62-74-8)

This material is super toxic. The probable oral lethal dose in humans is less than 5 mg/kg, or a taste (less than 7 drops) for a 150-lb. person. (EPA, 1998)

· Highly toxic, may be fatal if inhaled, ingested or absorbed through skin.

Hazards Summary · 1 Eintrag

A metabolic poison that combines with acetyl coenzyme A, causing the formation of fluorocitrate, which disrupts the Krebs cycle; Symptoms usually begin within 3 hours of ingestion. Patients die from ventricular fibrillation, frequently associated with hypokalemia and hypocalcemia. [Ford, p. 856-7] Very toxic by inhalation of dust, skin absorption, or ingestion; [CHEMINFO] 5 mg/kg is the estimated lethal oral dose for humans. After a lethal dose, death is preceded by seizures and ventricular fibrillation. [ACGIH] Damages the liver and kidneys in poisoning cases; [Merck Index] Poisoning cases may resemble those caused by other cellular toxins (hydrogen cyanide and hydrogen sulfide), but onset of symptoms is usually slower for fluoroacetate; [Olson, p. 242]

DOT ID and Guide · 2 Einträge

2629 151

2629 151

Reactive GroupHalogenated Organic Compounds
EC ClassificationSymbol: T+, N; R: 26/27/28-50; S: (1/2)-13-22-36/37-45-61; Note: A
UN ClassificationUN Hazard Class: 6.1; UN Pack Group: I
Special Reports · 2 Einträge

USEPA; Chemical Profile: Sodium Fluoroacetate (1985). Aspects covered in this data sheet: chemical identity; exposure limits; physicochemical properties; fire and explosion hazards; reactivity; health hazards; uses; handling of spills or releases.

USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document - Sodium Fluoroacetate EPA 738-R-95-025 (September 1995). The RED summarizes the risk assessment conclusions and outlines any risk reduction measures necessary for the pesticide to continue to be registered in the U.S.[Available from, as of February 10, 2014: http://www.epa.gov/pesticides/reregistration/status.htm]

Sicherheit und Schutzausrüstung

Fire Fighting · 2 Einträge

Stay upwind; keep out of low areas. Wear self-contained, positive pressure breathing apparatus and full protective clothing.

In case of fire in the surroundings, use appropriate extinguishing media.

First Aid Measures · 4 Einträge

Fresh air, rest. Refer for medical attention.

Rinse skin with plenty of water or shower. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention .

Accidental Release Measures · 2 Einträge

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· Do not touch damaged containers or spilled material unless wearing appropriate protective clothing.

First Aid · 3 Einträge

Warning: Effects usually appear within 30 minutes of exposure but may be delayed as long as 20 hours. Caution is advised. Vital signs should be monitored closely.

General First Aid:

(General first aid procedures)

Safe StorageSeparated from food and feedstuffs. Well closed.
Exposure Control and Personal Protection · 2 Einträge

· Wear positive pressure self-contained breathing apparatus (SCBA).

0.05 [mg/m3], inhalable fraction[German Research Foundation (DFG)]

Fire Fighting Procedures · 3 Einträge

Wear self contained breathing apparatus for fire fighting if necessary.

If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use foam, dry chemical, or carbon dioxide. Keep run-off water out of sewers and water sources.

Extinguish small fires: dry chemical, carbon dioxide, water spray, or foam; large fires: water spray, fog, or foam. Move container from fire area if you can do so without risk.

Storage ConditionsYou should store this chemical under refrigerated temperatures and away from mineral acids and bases.
Cleanup Methods · 2 Einträge

Wear respiratory protection. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust.

1) Ventilate area of spill. 2) Collect spilled material in most convenient & safe manner & deposit in sealed containers for reclamation or for disposal in secured sanitary landfill. Liquid containing sodium fluoroacetate should be absorbed in vermiculite, dry sand, earth, or similar material.

Nonfire Spill ResponseExcerpt from ERG Guide 151 [Substances - Toxic (Non-Combustible)]:
Disposal Methods · 3 Einträge

Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number P058, must conform with USEPA regulations in storage, transportation, treatment and disposal of waste.

SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.

A poor candidate for incineration.

Spillage Disposal · 1 Eintrag

Evacuate danger area! Consult an expert! Personal protection: chemical protection suit including self-contained breathing apparatus. Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.

Toxikologische Informationen

Treatment · 1 Eintrag

Because of the biochemical interference in the citric acid cycle, sodium fluoroacetate poisoning is very difficult to treat. Once clinical symptoms are exhibited, the citric acid cycle has shut down. Effective antidotes are unknown. Research in animals has shown that the use of glyceryl monoacetate can prevent problems if given after ingestion of sodium fluoroacetate. In clinical cases, use of muscle relaxants, anti-convulsants, mechanical ventilation, and other supportive measures may all be required. Few animals or people have been treated successfully after significant sodium fluoroacetate ingestions. (L1713)

Interactions · 1 Eintrag

Male Sprague-Dawley rats were injected ip with 376 mg diethylmaleate 30 min prior to ip admin of 1, 1.5, 2.5, 3.5, 4, 4.5, 5.5 or 7 mg/kg sodium fluoroacetate. Reduction of liver glutathione concentration by diethylmaleate pre-dosing caused 35% lowering in LD50 of sodium fluoroacetate.

Target Organs · 2 Einträge

Cardiovascular

respiratory system, cardiovascular system, liver, kidneys, central nervous system

Ecotoxicity Values · 5 Einträge

LD50; Species: Raccoon oral 1.1 mg/kg

LD50; Species: /Peromyscus maniculatus/ (Deer Mouse) oral 4.0 mg/kg

LD50; Species: Skunk oral 1.0 mg/kg

LD50; Species: Cotton Rat oral 0.1 mg/kg

For more Ecotoxicity Values (Complete) data for SODIUM FLUOROACETATE (37 total), please visit the HSDB record page.

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: When released to moist soil, sodium flouroacetate will dissociate to the fluoroacetate ion given a pKa of 2.72(1). The fluoroacetate anion is expected to be fairly mobile in soil(2). Volatilization from dry or moist soil surfaces is not expected and thus it will not partition to the atmosphere(SRC). As a class, fluoroacetates are slowly destroyed by soil bacteria but do not usually persist in soil for more than 2 months(3). Proposed soil biodegradation pathways for the free acid were the formation of glycollate or formation of oxaloacetate degrading to fluorocitrate(4).

AQUATIC FATE: When released to water, sodium fluoroacetate will form the fluoroacetate anion (pKa of 2.72(1)). The fluoroacetate anion is not expected to adsorb more strongly to suspended solids and sediments(2). Volatilization from water surfaces is not expected to be an important fate process because it is an anion in dissociated form. Following the addition of sodium fluoroacetate to a New Zealand-based stream water ecosystem model with Myriophyllum triphyllum, fluoroacetic acid was detected(3).

ATMOSPHERIC FATE: Because sodium fluoroacetate is a salt and forms the anion in water, it will not partition to the atmosphere. (SRC)

Adverse EffectsNeurotoxin - Other CNS neurotoxin
Exposure Routes · 2 Einträge

The substance can be absorbed into the body by inhalation, through the skin and by ingestion.

inhalation, skin absorption, ingestion, skin and/or eye contact

Toxicity Summary · 1 Eintrag

Fluoroacetate is similar to acetate, which has a pivotal role in cellular metabolism. Fluoroacetate disrupts the citric acid cycle by combining with coenzyme A to form fluoroacetyl CoA. Fluoroacetyl CoA then reacts with citrate synthase to produce fluorocitrate. A metabolite of fluorocitrate binds very tightly to aconitase, thereby halting the citric acid cycle. This inhibition results in an accumulation of citrate in the blood which deprives cells of energy. (L1713)

Ecotoxicity Excerpts · 5 Einträge

/BIRDS and MAMMALS/ Genetic resistance seemed to have developed among some animals grazing on fluoroacetate rich vegetation of western Australia. The concentration of fluoride ion (F-) in plasma of western gray kangaroo (Macropus fuliginosus ocydromus) following feeding of fluoroacetate was increased suggesting detoxication involving substantial defluorination of fluoroacetate or one of its metabolites. Elevation of plasma citrate following oral administration of 5 mg fluoroacetate/kg in gray kangaroos were much less than eastern red kangaroo (Megleia rufa).

/BIRDS and MAMMALS/ A total of 83 black-tailed prairie dogs from South Dakota were dosed with 0.01, to 0.30 mg/kg of sodium fluoroacetate. The animals were then allowed food and water, and observations were recorded at 8-hour intervals for a minimun of 96 hours post treatment. Animals that survived the initial dosage were administered additional dosages at 3-week intervals until death. The acute oral LD50 was established at 0.173 mg/kg.

/BIRDS and MAMMALS/ Poisoning of dogs is possible because of their extreme susceptibility to 1080. Poisoning of birds is less likely. The risk of secondary poisoning is reduced as the concentration of 1080 declines in putrefying carcasses.

/BIRDS and MAMMALS/ In adult starlings (Sturnus vulgaris) fed compound 1080 at 27-432 ppm, very high toxicity was noted. The 5 day lethal concentration was 4.7 ppm. The average testis weight was slightly decreased.

For more Ecotoxicity Excerpts (Complete) data for SODIUM FLUOROACETATE (14 total), please visit the HSDB record page.

Plant Concentrations · 1 Eintrag

Sodium fluoroacetate (compound 1080) is applied as a vertebrate pesticide in New Zealand for control of introduced mammalian pests. Despite its widespread use, little is known about the soil ecotoxicity of 1080. Therefore, the hazard of 1080 to soil invertebrates, plants, and soil microorganisms was evaluated in a series of controlled laboratory tests. ... Lettuce (Lactuca sativa) was more sensitive than oats (Avena sativa) to 1080. Lettuce seedling emergence and seedling shoot growth were adversely affected at a soil concentration of 7 mg/kg. The presence of 1080 in soil at concentrations up to 1 g/kg soil did not affect the ability of soil microorganisms to mineralize nitrogen. Furthermore, nitrate mineralization was not inhibited in soil treated with the urine of 1080-poisoned possums (Trichosurus vulpecula). The data collectively indicate that 1080-related effects on soil organisms occur at levels well above those that have been measured in soil (<0.1 mg/kg) following application of 1080 in baits for vertebrate pest control in New Zealand.

Signs and Symptoms · 5 Einträge

Convulsions. Laboured breathing. Unconsciousness.

MAY BE ABSORBED! See Inhalation.

See Inhalation.

vomiting; anxiety, auditory hallucinations; facial paresthesia; twitching face muscle; pulsus altenans, ectopic heartbeat, tachycardia, cardiac arrhythmias; pulmonary edema; nystagmus; convulsions; liver, kidney damage

The symptoms of sodium fluoroacetate poisoning normally appear between 30 minutes and three hours after exposure. Initial symptoms typically include nausea, vomiting and abdominal pain; sweating, confusion and agitation follow. In significant poisoning cardiac abnormalities including tachycardia or bradycardia, hypotension and ECG changes develop. Neurological effects include muscle twitching and seizures. Consciousness becomes progressively impaired after a few hours leading to coma. Death is generally due to ventricular arrhythmias, progressive hypotension unresponsive to treatment, and secondary lung infections. Sub-lethal doses of sodium fluoroacetate may cause damage to tissues with high energy needs, in particular, the brain, gonads, heart, lungs and fetus. Sub-lethal doses are typically completely metabolised and excreted within four days. (L1713)

Ongoing Test Status · 1 Eintrag

EPA has released the first beta version (version 0.5) of the Interactive Chemical Safety for Sustainability (iCSS) Dashboard. The beta version of the iCSS Dashboard provides an interactive tool to explore rapid, automated (or in vitro high-throughput) chemical screening data generated by the Toxicity Forecaster (ToxCast) project and the federal Toxicity Testing in the 21st century (Tox21) collaboration. /The title compound was tested by ToxCast and/or Tox21 assays; See the data in Chemical Explorer/[USEPA; ICSS Dashboard Application; Available from, as of March 28, 2014: http://actor.epa.gov/dashboard/]

Regulatorische Informationen

RCRA Requirements · 1 Eintrag

P058; As stipulated in 40 CFR 261.33, when fluoroacetic acid sodium salt as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to federal and/or state hazardous waste regulations. Also defined as a hazardous waste is any container or inner liner used to hold this waste or any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5(e)).

TSCA Requirements · 1 Eintrag

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Sodium fluoroacetate is included on this list. Effective date: 3/7/86; Sunset date: 3/7/96.

FIFRA Requirements · 4 Einträge

Classified for restricted use and limited to use by or under the direct supervision of a certified applicator. Formulation: All solutions and dry baits; Use Pattern: All uses; Classification: Restricted; Criteria Influencing Restriction: Acute oral toxicity. Hazard to nontarget organisms. Use and accident history.

Cancelled all products except those used for livestock collars for predicide use & control of certain rodents in CA & CO (Uses are currently under review). Criteria of concern: Reduction in nontarget & endangered species. Reference: PR Notice 72-2 3/9/72. 10th Circuit court's Vacation of Wyoming District Court's Predicide Injunction, 12/2/75/ 49 FR 4830 2/5/83; 50 FR 31012 7/31/85.

Based on the reviews of the generic data for the active ingredient sodium fluoroacetate, the Agency has sufficient information on the health effects of sodium fluoroacetate and on its potential for causing adverse effects in fish and wildlife and the environment. The Agency has determined that sodium fluoroacetate products, labeled and used as specified in this Reregistration Eligibility Decision, will not pose unreasonable risks or adverse effects to humans or the environment. Therefore, the Agency concludes that products containing sodium fluoroacetate registered for the sole remaining use are eligible for reregistration.

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer saftey standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Sodium fluoroacetate is found on List C. Case No: 3073; Pesticide type: insecticide, rodenticide; Case Status: RED Approved 06/95; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): sodium fluoroacetate; Data Call-in (DCI) Date(s): 10/02/92; AI Status: OPP has completed a Reregistration Eligibility Decision (RED) for the case/AI.

CERCLA Reportable Quantities · 2 Einträge

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 10 lb or 4.54 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV.D.3.b).

Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Sodium fluoroacetate is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 10 or 10,000 lbs. Extremely hazardous substances that are solids are subject to either of two threshold planning quantities ... The lower quantity applies only if the solid exists in powdered form and has a particle size less than 100 microns; or is handled in solution or in molten form; or meets the criteria for a National Fire Protection Association (NFPA) rating of 2, 3 or 4 for reactivity. If the solid does not meet any of these criteria, it is subject to the upper ... threshold planning quantity ... .

Sicherheitsdaten

F
3
OEB
D
OEL
TWA: 0.05 mg/m3, STEL: 0.15 mg/m3 [skin]
wgk
3
IDLA
2.5 mg/m3
tsca
TSCA listed
ridadr
UN 2629
hs_code
29159000
RTECS-Nr.
AH9100000
risk_code
26/27/28-50
hazard_code
T+,N,T
hazard_note
Highly Toxic
safety_code
13-22-36/37-45-61
hazard_class
6.1
packing_group
I
Giftige Stoffe Daten
62-74-8(Hazardous Substances Data)

Sodium fluoroacetate was introduced as a rodenticide in the US in 1946. However, its considerable efficacy against target species is offset by comparable toxicity to other mammals and, to a lesser extent, birds and its use as a general rodenticide was therefore severely curtailed by 1990. Currently, sodium fluoroacetate is licensed in the US for use against coyotes, which prey on sheep and goats, and in Australia and New Zealand to kill unwanted introduced species. The extreme toxicity of fluoroacetate to mammals and insects stems from its similarity to acetate, which has a pivotal role in cellular metabolism. Fluoroacetate combines with coenzyme A (CoA-SH) to form fluoroacetyl CoA, which can substitute for acetyl CoA in the tricarboxylic acid cycle and reacts with citrate synthase to produce fluorocitrate, a metabolite of which then binds very tightly to aconitase, thereby halting the cycle. Many of the features of fluoroacetate poisoning are, therefore, largely direct and indirect consequences of impaired oxidative metabolism. Energy production is reduced and intermediates of the tricarboxylic acid cycle subsequent to citrate are depleted. Among these is oxoglutarate, a precursor of glutamate, which is not only an excitatory neurotransmitter in the CNS but is also required for efficient removal of ammonia via the urea cycle. Increased ammonia concentrations may contribute to the incidence of seizures. Glutamate is also required for glutamine synthesis and glutamine depletion has been observed in the brain of fluoroacetate-poisoned rodents. Reduced cellular oxidative metabolism contributes to a lactic acidosis. Inability to oxidise fatty acids via the tricarboxylic acid cycle leads to ketone body accumulation and worsening acidosis. Adenosine triphosphate (ATP) depletion results in inhibition of high energy-consuming reactions such as gluconeogenesis. Fluoroacetate poisoning is associated with citrate accumulation in several tissues, including the brain. Fluoride liberated from fluoroacetate, citrate and fluorocitrate are calcium chelators and there are both animal and clinical data to support hypocalcaemia as a mechanism of fluoroacetate toxicity. However, the available evidence suggests the fluoride component does not contribute. Acute poisoning with sodium fluoroacetate is uncommon. Ingestion is the major route by which poisoning occurs. Nausea, vomiting and abdominal pain are common within 1 hour of ingestion. Sweating, apprehension, confusion and agitation follow. Both supraventricular and ventricular arrhythmias have been reported and nonspecific ST- and T-wave changes are common, the QTc may be prolonged and hypotension may develop. Seizures are the main neurological feature. Coma may persist for several days. Although several possible antidotes have been investigated, they are of unproven value in humans. The immediate, and probably only, management of fluoroacetate poisoning is therefore supportive, including the correction of hypocalcaemia.

For more Mechanism of Action (Complete) data for SODIUM FLUOROACETATE (7 total), please visit the HSDB record page.

Biological Half-Life · 2 Einträge

Plasma elimination half-life in rabbits was shown to be 1.1 hour and the retention time in tissue greater with larger doses. Tissue residues were substantially lower than in plasma.

Sodium monofluoroacetate (1080) was administered orally to sheep and goats at a dose level of 0.1 mg/kg bw. The plasma elimination half-life was 10.8 hr in sheep and 5.4 hr in goats.

Metabolism/Metabolites · 5 Einträge

Following injection of fluoroacetate-2-(14)C into rats, about 3% of label appeared in respiratory carbon dioxide and 32% in urine within 4 days. Labeled fluorocitrate was recovered from urine. Incorporation of label into cholesterol and into... lower and higher fatty acid fractions was demonstrated. Other unidentified labeled materials /were/... observed.

When fluoroacetate-2-(14)C was applied to plants (acacia geoginae, castor bean, peanut, pinto bean), labeled carbon monoxide was observed. Some label... was also incorporated into water soluble fractions and lipids. In some plant seeds... /it/ was converted into fluorine-containing long chain fatty acids.

Sodium fluoroacetate is converted into fluorocitric acid in body and blocks TCA cycle by inhibiting aconitase activity. Poisoning can be diagnosed by increased citric acid levels in all organs or by determination of aconitase activity.

2,4-Dinitrofluorobenzene reacts with glutathione to form a stable product similar to that formed with the model glutathione-S-transferase substrate, 1-chloro-2,4-dinitrobenzene. ... Fluoroacetamide, like fluoroacetate, undergoes no discernable chemical defluorination. Its enzymatic defluorination is approx 10% of that observed for fluoroacetate and only 0.2% of the rate for 2,4-dinitrofluorobenzene. An antibody raised to the fluoroacetate specific dehalogenase precipitated both fluoroacetate ad fluoroacetamide defluorinating activity but had no effect on either 1-chloro-2,4-dinitrobenzene or 2,4-dinitrofluorobenzene activity. ... 2,4-Dinitrofluorobenzene is metabolized by the glutathione-S-transferase while fluoroacetamide is metabolized by the fluoroacetate specific dehalogenase.

For more Metabolism/Metabolites (Complete) data for SODIUM FLUOROACETATE (7 total), please visit the HSDB record page.

MeSH Pharmacological ClassificationSubstances used to destroy or inhibit the action of rats, mice, or other rodents.
Absorption, Distribution and Excretion · 5 Einträge

... Rapidly absorbed by GI tract. It is not well absorbed by intact skin, but absorption may be greater in presence of dermatitis or other skin injury.

... Samples taken at autopsy from man who survived about 17 hours after being found unconscious ... /showed concn in/ urine, 368 ppm; liver, 58 ppm; brain, 76 ppm; and kidney, 65 ppm.

...Liver of person whose death was supposed due to sodium fluoroacetate contained 2.4 mg of fluorine/100 g.

Amount of sodium monofluoroacetate recovered from brain per unit weight of tissue was about 2 times that from other organs after rabbits were killed with dose 10 times LD50. Amount of organofluorine was about the same 24 hr after death as immediately after death and decreased gradually, by 10-20% after 3 days and by 50-80% when carcass was kept at 21-25 °C.

For more Absorption, Distribution and Excretion (Complete) data for SODIUM FLUOROACETATE (8 total), please visit the HSDB record page.

Verwendung und Herstellung

Uses · 6 Einträge

Used to eliminate coyotes and rodents; [ACGIH]

Use restricted in the US to livestock collars to protect sheep and cattle from coyotes; Used to control vertebrates in Australia and New Zealand; [Olson, p. 242]

Farming (Pesticides) [Category: Industry]

For sodium fluoroacetate (USEPA/OPP Pesticide Code: 075003) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Rodenticide

Predacide ... Product kills coyotes preying on sheep and goats.

Methods of Manufacturing · 5 Einträge

Condensing methyl chloroacetate with potassium fluoride and then converting the fluoroester to the sodium salt with NaOH.

Reacting CO, HF and formaldehyde at high pressures to give fluoroacetic acid which is converted by NaOH to sodium fluoroacetate.

Ethyl chloroacetate and potassium fluoride form ethyl fluoroacetate, which is then treated with a methanol solution of sodium hydroxide.

Sodium fluoroacetate is usually made by displacing the halogen from an ester of bromo- or chloroacetic acid with potassium fluoride or, in one instance, antimony fluoride, followed by hydrolysis with aqueous sodium hydroxide.

A commercial process for ... manufacture from ethyl chloroacetate and potassium fluoride has been described. The ester, purified by distillation to remove traces of acid and water, is treated with oven-dried, finely powdered potassium fluoride in a well-stirred autoclave at 200 °C for 11 hours. The resulting ethyl fluoroacetate is then distilled into an agitated tank containing sodium hydroxide dissolved in methanol. The solid product is isolated by centrifugation, followed by vacuum drying.

Formulations/Preparations · 5 Einträge

Usually marketed as water soln containing 0.5% nigrosine as black warning color. 90% Powder. Usually in locked bait boxes.

Bait concentrate

Collar: 1% a.i. available. All Collars contain 1.1 oz of formulated material which is equal to approximately 0.00067 lbs a.i./collar.

Compound 1080 Livestock Protection Collar (SD Dept of Agriculture): Active ingredient: Sodium fluoroacetate 1.04%.

For more Formulations/Preparations (Complete) data for SODIUM FLUOROACETATE (9 total), please visit the HSDB record page.

General Manufacturing Information · 3 Einträge

Acetic acid, 2-fluoro-, sodium salt (1:1): ACTIVE

The WHO Recommended Classification of Pesticides by Hazard identifies sodium fluoroacetate (technical grade) as Class IA: extremely hazardous; Main Use: rodenticide.

The extreme toxicity of /sodium fluoroacetate (compound 1080) and fluoroacetamide (compound 1081)/... has restricted their use to prepared baits.

Anwendungen

VerwendenSodium fluoroacetate is used for rodent control in restricted environments and for the control of the brushtail possum and other wild mammals in some countries.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

2-FluoracetamidMethylfluoracetatEthylfluoracetat

Nachgelagerte Produkte

MonofluoressigsäureFormaldehyd