Chlordecon (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
WEISSE KRISTALLE.
CHEMISCHE GEFAHREN
Beim Verbrennen Bildung von Chlordämpfen und Chlorwasserstoff. Zersetzung bei Kontakt mit Säuren unter Bildung giftiger Rauche.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK: Krebserzeugend Kategorie 3B; (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper über die Haut, durch Verschlucken und durch Inhalation.
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Dispergieren schnell erreicht werden.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Möglich sind Auswirkungen auf Zentralnervensystem und Leber mit nachfolgenden Funktionsstörungen und Leberschäden. Die Auswirkungen treten u.U. verzögert ein.
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Wiederholter oder andauernder Hautkontakt kann Dermatitis hervorrufen. Möglich sind Auswirkungen auf das endokrine System. Möglicherweise krebserzeugend für den Menschen. Fruchtbarkeitsschädigend oder entwicklungsschädigend.
LECKAGE
Verschüttetes Material in Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Atemschutzgerät, P3-Filter für giftige Partikel.
R-Sätze Betriebsanweisung:
R24/25:Giftig bei Berührung mit der Haut und beim Verschlucken.
R40:Verdacht auf krebserzeugende Wirkung.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
Beschreibung
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).
Chemische Eigenschaften
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.
Physikalische Eigenschaften
Colorless to tan, odorless, noncombustible, crystalline solid
Verwenden
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.
Definition
ChEBI: An organochlorine compound with insecticidal activity.
Allgemeine Beschreibung
Odorless colorless crystalline solid.
Air & Water Reaktionen
Insoluble in water.
Reaktivität anzeigen
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.
Health Hazard
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.
Brandgefahr
Flash point data for KEPONE (TM) are not available; however, KEPONE (TM) is probably combustible.
mögliche Exposition
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.
Carcinogenicity
Kepone (chlordecone) is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.
Environmental Fate
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.
Versand/Shipping
UN2761 Organochlorine pesticides, solid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
Inkompatibilitäten
Acids, acid fumes.
Waste disposal
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.
Chlordecon (ISO) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
