115-32-2

Pure dicofol is available as a white or gray powder or colorless solid crystals while the technical dicofol is a red-brown or amber viscous liquid with an odor 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 a persistent OCP used as an acaricide and miticide. It is structurally similar to DDT. Dicofol is combustible and incompatible with strong oxidizing agents. It is soluble in most aliphatic and aromatic solvents and most common organic solvents, but practically insoluble in water and hydrolyzes in basic solution. It is used on a wide variety of fruit, vegetables, ornamental and fi eld crops. Dicofol is manufactured from DDT. Dicofol is corrosive to some metals. It is used for foliar applications, mostly on cotton, apples, and citrus crops. Other crops include strawberries, mint, beans, peppers, tomatoes, pecans, walnuts, stonefruit, cucurbits, and non-residential lawns/ornamentals.

DICOFOL(115-32-2) 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(115-32-2) is a liquid DICOFOL(115-32-2) can easily penetrate the soil and contaminate groundwater and nearby streams. DICOFOL(115-32-2) can cause illness by inhalation, skin absorption, and/or ingestion. DICOFOL(115-32-2) is used as a pesticide.

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. .

Hydrolyzed in alkaline media to dichlorobenzophenone and chloroform. Insoluble in water.

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.

Inhalation or ingestion causes nausea, headache, weight loss, convulsions, possible kidney and liver damage. Contact with eyes causes irritation.

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.

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit

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.

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

Dicofol is a white or brown waxy solid.Molecular weight=370.48; Flash point=120℃. HazardIdentification (based on NFPA-704 M Rating System):Health 2, Flammability 1, Reactivity 0. Slightly soluble inwater.

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.

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.

Nonsystemic acaricide to control mites in citrus fruits, grapes, cotton, pome and stone fruit.

ChEBI: A tertiary alcohol that is DDT in which the benzylic hydrogen has been replaced by a hydroxy group.

Dicofol is commercially produced through a multi-step synthesis that begins with technical-grade DDT. The process involves the chlorination of DDT to form Cl-DDT, followed by hydrolysis to yield dicofol. To improve environmental safety and reduce impurities, modern methods often include recrystallisation steps using solvents like acetic acid or alkanes to isolate the active p,p′-dicofol isomer while minimising the presence of the less active o-p′ isomer and residual DDT.

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.

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

Non-systemic with contact action. Disrupts the nervous system of mites - a CNS toxin.

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

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.

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with dicofolyou should be trained on its proper handling and storage.Store in tightly closed containers in a cool, well-ventilatedarea away from alkaline pesticides, strong acids, acidfumes, and steel. Where possible, automatically transfermaterial from drums or other storage containers to processcontainers. A regulated, marked area should be establishedwhere this chemical is handled, used, or stored in compliance with OSHA Standard 1910.1045.

Dicofol is stable to acids but unstable in alkaline media in which it is hydrolysed to 4,4’-dichlorobenzophenone(2) and chloroform (DT₅₀ values at pH 5, 7 and 9 are 85 days, 64-99 hours and 26 minutes, respectively). The isomer, 2,2,2-trichloro-1-(2-chlorophenyl)-1-(4-chlorophenyl)ethanol (o,p’-dicofol), is hydrolysed more rapidly.
Dicofol is degraded by light to 4,4’-dichlorobenzophenone (2) (PM).

Acaricide