1,1a,3,3a,4,5,5,5a,5b,6-デカクロロ-1,1a,3,3a,4,5,5a,5b-オクタヒドロ-1,3,4-メテノ-2H-シクロブタ[cd]ペンタレン-2-オン

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H301：飲み込むと有毒

  H311：皮膚に接触すると有毒

  H351：発がんのおそれの疑い

  H410：長期的影響により水生生物に非常に強い毒性

• 注意書き

  P273：環境への放出を避けること。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P301+P310：飲み込んだ場合：直ちに医師に連絡すること。

  P312：気分が悪い時は医師に連絡すること。

  P501：内容物/容器を．．．に廃棄すること。

1,1a,3,3a,4,5,5,5a,5b,6-デカクロロ-1,1a,3,3a,4,5,5a,5b-オクタヒドロ-1,3,4-メテノ-2H-シクロブタ[cd]ペンタレン-2-オン 価格

1,1a,3,3a,4,5,5,5a,5b,6-デカクロロ-1,1a,3,3a,4,5,5a,5b-オクタヒドロ-1,3,4-メテノ-2H-シクロブタ[cd]ペンタレン-2-オン 化学特性,用途語,生産方法

• 用途

  殺菌剤、防かび剤、防汚剤、殺虫剤、防虫剤

• 説明

  Chemically, kepone is a chlorinated polycyclic insecticide and fungicide. Chlordecone was used as an insecticide for leaf-eating insects, ants, and cockroaches; as a larvicide for flies; and for control of insects that attack structures. Chlordecone was also used on bananas, nonbearing citrus trees, tobacco, ornamental shrubs, lawns, turf, and flowers. The dry powder is readily absorbed through the skin and respiratory tract. Occupational workers handling kepone without appropriate workplace safety dress and PPE suffered chemical poisoning. The symptoms included, tremors, jerky eye movements, memory loss, headaches, slurred speech, unsteadiness, lack of coordination, loss of weight, rash, enlarged liver, decreased libido, sterility, chest pain, and arthralgia (sharp pain, extending along a nerve or group of nerves, experienced in a joint and/or joints). Chlordecone was first introduced as a pesticide in 1958 and was used until 1978, when its use in the United States was discontinued (NCI 1976, IARC 1979, HSDB 2009).

• 化学的特性

  Kerosene is a white to pale yellow, flammable liquid that has wide use in household and industrial activities. For instance, in heating, as cooking fuel, in cleaning, degreasing, as a solvent, for paints, enamels, polishes, varnishes, and in asphalt coating.

• 物理的性質

  Colorless to tan, odorless, noncombustible, crystalline solid

• 使用

  Chlordecone, a chlorinated dicyclodiene compound, was introduced under the trade name Kepone in 1958. In the United States, Kepone found use as an ant and cockroach poison. Outside the United States, it was used primarily as a pesticide against the banana root borer. The compound is the ketone analog of mirex; it is a contaminant of mirex and is also a product of mirex degradation.

• 定義

  ChEBI: An organochlorine compound with insecticidal activity.

• 一般的な説明

  Odorless colorless crystalline solid.

• 空気と水の反応

  Insoluble in water.

• 反応プロフィール

  A halogenated ketone. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

• 健康ハザード

  INHALATION AND INGESTION: These symptoms present in all affected patients - Neurologic Impairment - anxiety, irritability, memory disturbance, headache, tremors, opsiclonus, stuttering, slurred speech, and abnormal tandem gait.

• 火災危険

  Flash point data for KEPONE (TM) are not available; however, KEPONE (TM) is probably combustible.

• 職業ばく露

  Kepone was registered for the control of rootborers on bananas with a residue tolerance of 0.01 ppm. This constituted the only food or feed use of Kepone. Nonfood uses included wireworm control in tobacco fields and bait to control ants and other insects in indoor and outdoor areas. A rebuttable presumption against registration of chlordecone was issued by the United States Environmental Protection Agency on March 25, 1976 on the basis of oncogenicity. The trademarked Kepone and products of six formulations were the subject of voluntary cancellation according to a United States Environmental Protection Agency notice dated July 27, 1977. In a series of decisions, the first of which was issued on June 17, 1976, the EPA effectively canceled all registered products containing Kepone as of May 1, 1978.

• 発がん性

  Kepone (chlordecone) is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

• 環境運命予測

  Photolytic. Kepone-contaminated soils from a site in Hopewell, VA were analyzed by GC/MS. 8-Chloro and 9-chloro homologs identified suggested these were photodegradation products of kepone (Borsetti and Roach, 1978). Products identified from the photolysis of kepone in cyclohexane were 1,2,3,4,6,7,9,10,10-nonachloro-5,5-dihydroxypentacyclo[ 5.3.0.02,6.03,9.04,8]decane for the hydrate and 1,2,3,4,6,7,9,10,10-nonachloro-5,5- dimethoxypentacyclo[5.3.0.02,6.03,9.04,8]decane (Alley et al., 1974).
  Chemical/Physical. Readily reacts with moisture forming hydrates (Hollifield, 1979). Decomposes at 350°C (Windholz et al., 1983) probably emitting toxic chlorine fumes.

• 輸送方法

  UN2761 Organochlorine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

• 不和合性

  Acids, acid fumes.

• 廃棄物の処理

  A process has been developed which effects chlordecone degradation by treatment of aqueous wastes with UV radiation in the presence of hydrogen in aqueous sodium hydroxide solution. Up to 95% decomposition was effected by this process. Chlordecone previously presented serious disposal problems because of its great resistance to bio- and photo degradation in the environment. It is highly toxic to normally occur in degrading microorganisms. Although it can undergo some photodecomposition when exposed to sunlight to the dihydro compound (leaving a compound with 8 chloro substituents) that degradation product does not significantly reduce toxicity. Disposal by incineration with HCl scrubbing is recommended.

1,1a,3,3a,4,5,5,5a,5b,6-デカクロロ-1,1a,3,3a,4,5,5a,5b-オクタヒドロ-1,3,4-メテノ-2H-シクロブタ[cd]ペンタレン-2-オン 生産企業

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143-50-0, 1,1a,3,3a,4,5,5,5a,5b,6-デカクロロ-1,1a,3,3a,4,5,5a,5b-オクタヒドロ-1,3,4-メテノ-2H-シクロブタ[cd]ペンタレン-2-オン キーワード