Dicofol (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
FARBLOSE KRISTALLE.
CHEMISCHE GEFAHREN
Zersetzung beim Verbrennen oder bei Kontakt mit S?uren, S?urerauchen oder Basen unter Bildung giftiger und ?tzender Rauche mit Chlorwasserstoff.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den K?rper durch Inhalation des Aerosols, über die Haut und durch Verschlucken.
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachl?ssigbar; eine gesundheitssch?dliche Partikelkonzentration in der Luft kann jedoch beim Dispergieren schnell erreicht werden, vor allem als Pulver.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen und die Haut(technischer Grad). M?glich sind Auswirkungen auf Zentralnervensystem, Leber und Nieren.
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Wiederholter oder andauernder Hautkontakt kann Dermatitis hervorrufen.
LECKAGE
Verschüttetes Material in abgedeckten Beh?ltern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgf?ltig sammeln. An sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Pers?nliche Schutzausrüstung: Vollschutzanzug mit umgebungsluftunabh?ngigem Atemschutzger?t.
R-S?tze Betriebsanweisung:
R21/22:Gesundheitssch?dlich bei Berührung mit der Haut und beim Verschlucken.
R38:Reizt die Haut.
R43:Sensibilisierung durch Hautkontakt m?glich.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R11:Leichtentzündlich.
S-S?tze Betriebsanweisung:
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S60:Dieses Produkt und sein Beh?lter sind als gef?hrlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Beh?lter dicht geschlossen halten.
Chemische Eigenschaften
Pure dicofol is available as a white or grey powder or colourless crystal solid, while the technical dicofol is a red-brown or amber viscous liquid with an odour like fresh-cut hay. Dicofol undergoes decomposition on burning or on contact with acids, acid fumes, or bases producing toxic and corrosive fumes including hydrogen chloride.
Dicofol is combustible and incompatible with strong oxidising agents. Dicofol is soluble in most aliphatic and aromatic solvents and most common organic solvents but practically insoluble in water and hydrolyses in basic solution.
Verwenden
Acaricide, organochlorine pesticide. Dicofol is a non-systemic acaricide/miticide currently registered in the US and Canada for use on a wide variety of crops.
Definition
ChEBI: A tertiary alcohol that is DDT in which the benzylic hydrogen has been replaced by a hydroxy group.
Allgemeine Beschreibung
Dicofol or kelthane is a white crystalline, wettable powder dissolved in a liquid carrier, (water). The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since Dicofol is a liquid Dicofol can easily penetrate the soil and contaminate groundwater and nearby streams. Dicofol can cause illness by inhalation, skin absorption, and/or ingestion. Dicofol is used as a pesticide.
Air & Water Reaktionen
Hydrolyzed in alkaline media to dichlorobenzophenone and chloroform. Insoluble in water.
Reaktivit?t anzeigen
Dicofol is an organochlorine bridged diphenyl. Halogenated aliphatic compounds are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Halogenated aliphatics are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. Dicofol hydrolyzes in alkali. Dicofol is slightly corrosive to metals. Contact with steel at elevated temperatures causes formation of toxic gases. .
Health Hazard
Exposures to dicofol cause adverse health effects and poisoning. Occupational workers
suffer harmful effects on inhalation, ingestion and through skin contact. The symptoms
of poisoning include, but are not limited to, nausea, dizziness, weakness, and vomiting
from ingestion or respiratory exposure, skin irritation or rash from dermal exposure.
Dicofol-poisoned occupational workers show skin sensitization, conjunctivitis of the eyes,
and pathomorphological changes in the liver, kidneys, and CNS. After exposures to high
concentrations of dicofol, workers show nervousness, hyperactivity, headache, nausea,
vomiting, unusual sensations, fatigue, convulsions, coma, respiratory failure, and death.
However, published literature is limited and more data is required on occupational workers
as well as the general population.
Landwirtschaftliche Anwendung
Insecticide, Acaricide: Not approved for use in EU countries. Severely
Restricted for use in EU (containing>78% p,p'-dicofol or
1 g/kg of DDT and DDT-related compounds). Dicofol is
an organochlorine miticide/pesticide used for foliar applications,
mostly on cotton, apples, and citrus crops. Other
crops include: strawberries, mint, beans, peppers, tomatoes,
pecans, walnuts, stonefruit, cucurbits, and nonresidential
lawns/ornamentals. Formulations registered
for use on food/feed crops include emulsifiable concentrates,
and wettable powder formulations. These formulations
may be applied as concentrated or dilute sprays
using aircraft, duster, groundboom, and sprayer. Dicofol
is manufactured from DDT. In 1986, use of dicofol was
temporarily canceled by the U.S. EPA because of concerns
raised by high levels of DDT contamination. However,
it was reinstated when it was shown that modern manufacturing
processes can produce technical-grade dicofol
which contains <0.1% DDT.
Handelsname
ACARIN®[C]; CALLIFOL®; CARBAX®;
CEKUDIFOL®; DECOFOL®; DICOMITE®; DIFOL®;
FERRIAMICIDE®; FUMITE DICOFOL®; FW
293®; HIFOL®; KELTANE®; KELTHANE®; P,P'-
KELTHANE®; KELTHANETHANOL®; MILBOL®;
MITIGAN®; TIKTOK®; VAPCOTHION®, dicofol
m?gliche Exposition
A potential danger to those
involved in manufacture, formulation and application of
this organochlorine pesticide. Used as acaricide (miticide)
in agricultural and nonagricultural applications. Similar
in structure to DDT.
Environmental Fate
Plant. The major metabolite reported on apples is 4,4′-dichlorobenzophenone. On apples, dicofol concentrations decreased from 702 ppm to 436 ppm after 15 days. 4,4′Dichlorobenzophenone increased from 25.5 ppm at time of spraying to 25.5 ppm 15 days after spraying (Archer, 1974). Four days after spraying cucumbers with dicofol, residues decreased from 0.95–1.6 ppm to 0.4–1.5 ppm. No residues were detected 8 days after spraying (Nazer and Masoud, 1986). A half-life of 6 days was reported for dicofol in alfalfa (Akesson and Yates, 1964).
Chemical/Physical. When dicofol was exposed to sunlight for 20 days, a 10% yield of 4,4′-dichlorobenzophenone was obtained. Solvents containing dicofol and exposed to UV light resulted in the formation of chlorobenzilic acid esters (Vaidyanathasw
Stoffwechselwegen
Dicofol(1) is an analogue of DDT. However, the replacement of a hydrogen
atom at position 1 by a hydroxyl group results in a fundamental
change in chemical properties and increases the lability of the molecule. It
breaks readily down to 4,4’-dichlorobenzophenone (2) thermally or on
hydrolysis and this compound is a major metabolite in mammals and
plants.
Versand/Shipping
UN2996 Organochlorine pesticides, liquid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
UN3082 Environmentally hazardous substances, liquid, n.o.
s., Hazard class: 9; Labels: 9-Miscellaneous hazardous
material, Technical Name Required.
Inkompatibilit?ten
Incompatible with alkaline pesticides,
strong acids; acid fumes; aliphatic amines; isocyanates.
Halogenated aliphatic compounds are moderately or very
reactive. Halogenated organics generally become less reactive as more of their hydrogen atoms are replaced with halogen atoms. Halogenated aliphatics are incompatible with
strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds,
alkali metals, and epoxides. Dicofol hydrolyzes in alkali.
It is slightly corrosive to metals. Contact with steel at
elevated temperatures causes formation of toxic gases
Waste disposal
In accordance with
40CFR165, follow recommendations for the disposal of
pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting
your local or federal environmental control agency, or by
contacting your regional EPA office.
Dicofol (ISO) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Xylol, Isomerengemisch
Toluol-4-sulfonsure
2,2'-Dimethyl-2,2'-azodipropiono-nitril
Iodsure
Methansulfonsure
Chlor
DDT
EMULSIFIER
Natriumhydroxid
Schwefelsure
[2,2,2-trichloro-1,1-bis(4-chlorophenyl)ethyl] acetate
1,1-BIS(4-CHLOROPHENYL)-1,2,2,2-TETRACHLOROETHANE
Downstream Produkte
