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56073-10-0

56073-10-0 Structure

56073-10-0 Structure
IdentificationMore
[Name]

Brodifacoum
[CAS]

56073-10-0
[Synonyms]

3-(3-(4'-bromo-(1,1'-biphenyl)-4-yl)-1,2,3,4-tetrahydro-1-naphthyl)-4-hydroxy-2h-1-benzopyran-2-one
3-(3-(4'-Bromo-(1,1'-biphenyl)-4-yl)-1,2,3,4-tetrahydro-1-napthalenyl)-4-hydroxycoumarin
BROBAIT
BRODIFACOUM
FORWARAT
HAVOC
KLERAT
KLERAT(R)
MOUSE BAIT
NOFAR(R)
SOREX BRODIFACOUM RAT
TALON
TALON(R)
WEATHERBLOK(R)
2h-1-benzopyran-2-one,3-(3-(4’-bromo(1,1’-biphenyl)-4-yl)-1,2,3,4-tetrahydro-1
3-(3-(4’-bromo-1,1’-biphenyl-4-yl)-1,2,3,4-tetrahydro-1-naphthyl)-4-hydroxyc
3-(3-(4’-bromobiphenyl-4-yl)-1,2,3,4-tetrahydronaphth-1-yl)-4-hydroxycoumari
3-[3-(4’-bromo[1,1’-biphenyl]4-yl)-1,2,3,4-tetrahydro-1-naphthalenyl]-4-hydrox
3-[3-[4’-Bromo[1,1’-biphenyl]-4-yl]-1,2,3,4-tetrahydro-1-naphthalenyl]-4-hydroxy-2H-benzopyran-2-one
4-hydroxy-3-(3-(4’-bromo-4-biphenylyl)-1,2,3,4-tetrahydro-1-naphthyl)coumarin
[EINECS(EC#)]

259-980-5
[Molecular Formula]

C31H23BrO3
[MDL Number]

MFCD00084803
[Molecular Weight]

523.42
[MOL File]

56073-10-0.mol
Chemical PropertiesBack Directory
[Melting point ]

228-230°
[Boiling point ]

679.0±55.0 °C(Predicted)
[density ]

1.2940 (rough estimate)
[vapor pressure ]

41 x l0-6 Pa (20 °C)
[refractive index ]

1.4620 (estimate)
[storage temp. ]

0-6°C
[form ]

neat
[pka]

5.0 (weak acid, est.)
[Water Solubility ]

0.24 mg l-1 (20 °C)
[Merck ]

13,1363
[BRN ]

8171403
[CAS DataBase Reference]

56073-10-0(CAS DataBase Reference)
[EPA Substance Registry System]

56073-10-0(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

T+;N,N,T+
[Risk Statements ]

R27/28:Very Toxic in contact with skin and if swallowed .
R48/24/25:Toxic: danger of serious damage to health by prolonged exposure in contact with skin and if swallowed .
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S1/2:Keep locked up and out of the reach of children .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
[RIDADR ]

UN 2811
[WGK Germany ]

3
[RTECS ]

GN4934750
[HazardClass ]

6.1(a)
[PackingGroup ]

I
[Hazardous Substances Data]

56073-10-0(Hazardous Substances Data)
[Toxicity]

LD50 orally in male, female field rats: 0.16, 0.18 mg/kg (Yuet-Ming)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Potassium hydroxide-->Polyphosphoric acid-->Diethyl malonate-->Phosphorus tribromide-->Potassium borohydride-->4-Hydroxycoumarin-->Phenylacetyl chloride-->4-Bromobiphenyl-->1,2,3,4-Tetrahydro-1-naphthol
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Brodifacoum(56073-10-0).msds
Hazard InformationBack Directory
[Hazard]

Poison, anticoagulant.
[Description]

Brodifacoum is a 4-hydroxycoumarin anticoagulant that acts as a vitamin K antagonist. It was registered as a pesticide in 1979 in the United States although in 2008 it was made a restricted use pesticide by the Environmental Protection Agency. This means it can only be used by certified pesticide applicators; however, the makers of D-Con which contains 0.005% brodifacoum by weight have challenged this and brodifacoum is currently available in D-Con and in various other pesticide products for the eradication of mice and rats although it is also used on larger mammals such as possums. Brodifacoum currently remains available to the general public.
[Chemical Properties]

White Solid
[Uses]

Brodifacoum is a highly lethal vitamin K antagonist anticoagulant poison. In recent years, Broadifacoum, has become one of the world's most widely used pesticides.
[Uses]

Brodifacoum is used to control rodents in and around buildings.
[Uses]

Rodenticide.
[Definition]

ChEBI: Brodifacoum is a member of benzenes, a ring assembly and a member of naphthalenes.
[Environmental Fate]

Brodifacoum, like other hydroxycoumarins, interferes with the production of vitamin K–dependent coagulation factors. Vitamin K is a cofactor for the carboxylation of specific glutamic acid groups in coagulation factors II (prothrombin), VII, IX, and X. During this step, vitamin K is oxidized to vitamin K 2,3-epoxide. The regeneration of vitamin K by vitamin K 2,3-epoxide reductase is prevented by brodifacoum. As a result, dysfunctional decarboxy-coagulation factors are produced and coagulation is impaired. Brodifacoum is over 100 times more potent than warfarin on a molar basis in rats.
[Metabolic pathway]

The fate of brodifacoum in soils and plants has not been studied in detail because the compound is usually applied as a pelleted bait or in a wax block. This limits its dissipation in the environment. Studies in animals have been conducted as part of the assessment of safety and to investigate mode of action.
[Degradation]

Brodifacoum is a stable compound; no detectable degradation occurs at 50 °C or in direct sunlight over 30 days, though it is liable to some photodecomposition in solution.
[Toxicity evaluation]

Brodifacoum has a very low solubility in water and typically enters water through erosion where it is then found in the sediment. Brodifacoum concentrations are typically not measurable in water systems.
Products that contain brodifacoum as pesticide can remain toxic for a long period of time in the environment. The rate of decay of brodifacoum depends upon the amount of rainfall. As the product that contains brodifacoum degrades over time, the brodifacoum is absorbed into the soil. Soil bacteria degrade brodifacoum over weeks to months although soil type, temperature, and the presence of microorganisms that will degrade brodifacoum all influence the time it takes to degrade.
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