Acute toxicity - Category 4, Oral
Skin irritation, Category 2
Eye irritation, Category 2
Carcinogenicity, Category 2
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
H302 Harmful if swallowed
H315 Causes skin irritation
H319 Causes serious eye irritation
H351 Suspected of causing cancer
H410 Very toxic to aquatic life with long lasting effects
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P203 Obtain, read and follow all safety instructions before use.
P273 Avoid release to the environment.
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P321 Specific treatment (see ... on this label).
P332+P317 If skin irritation occurs: Get medical help.
P362+P364 Take off contaminated clothing and wash it before reuse.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P318 IF exposed or concerned, get medical advice.
P391 Collect spillage.
P405 Store locked up.
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest.
Remove contaminated clothes. To remove substance use polyethylene glycol 300 or vegetable oil. Rinse and then wash skin with water and soap.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Do NOT induce vomiting. Refer for medical attention .
SYMPTOMS: Symptoms of exposure to this compound may include irritation of the skin, eyes, nose, throat, mucous membranes and upper respiratory tract. Contact with the skin may result in redness, edema, dermatitis and chemical burns. Contact with the eyes may result in corneal injury and iritis. It may also cause lacrimation. Other symptoms may include an increase followed by a decrease in respiratory rate and urinary output, fever, increased bowel action, weakness of movement, collapse, convulsions, lung damage, liver damage and kidney damage. Additional symptoms caused by this type of compound include painless blanching or erythema of the skin, corrosion, profuse sweating, intense thirst, nausea and vomiting, diarrhea, cyanosis from methemoglobinemia, hyperactivity, hyperthermia, skin rashes (sometimes chloracne), neurological and immunological effects, stupor, blood pressure fall, hyperpnea, abdominal pain, hemolysis, coma, and pulmonary edema followed by pneumonia. Rapid death has been reported. If death from respiratory failure is not immediate, jaundice and oliguria or anuria may occur. Skin sensitivity reactions occur occasionally. Prolonged eye contact may cause eye damage. Depending on the intensity and duration of exposure, effects may include severe destruction of tissue. ACUTE/CHRONIC HAZARDS: This compound is harmful by ingestion, inhalation and skin absorption. It is an irritant of the skin, eyes, nose, throat, mucous membranes and upper respiratory tract. When heated to decomposition it emits toxic fumes of carbon monoxide, carbon dioxide and hydrogen chloride gas. It may also emit toxic fumes of chloride ion. (NTP, 1992)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Phenols and related compounds
If material /is/ involved in /a/ fire, extinguish fire using agent suitable for type of surrounding fire. Material itself does not burn or burns with difficulty. Trichlorophenol
Literature sources indicate that this chemical is nonflammable. (NTP, 1992)
Use foam, dry powder, carbon dioxide.
Personal protection: filter respirator for organic gases and particulates adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Personal protection: filter respirator for organic gases and particulates adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Activated carbon is a good method for removing chlorophenols from water. Competitive adsorption occurs between chlorophenols & humic substances present in nearly all municipal water supplies. This competition decr the capacity of carbon for chlorophenols. Chlorophenols
Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Provision to contain effluent from fire extinguishing. Separated from strong oxidants and food and feedstuffs. Well closed. Store in an area without drain or sewer access.PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. Chemical Carcinogens
Component | 2,4,6-trichlorophenol | |||
---|---|---|---|---|
CAS No. | 88-06-2 | |||
Limit value - Eight hours | Limit value - Short term | |||
ppm | mg/m3 | ppm | mg/m3 | |
Denmark | ? | 0,5 | ? | 1 |
Sweden | ? | 0,5 | ? | 1,5 (1) |
Remarks | ||||
Sweden | (1) 15 minutes average value |
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear safety goggles or face shield.
Protective gloves. Protective clothing.
Use ventilation (not if powder), local exhaust or breathing protection.
no data available
PHYSICAL DESCRIPTION: Yellow to pinkish-orange needles or orange fluffy solid. Strong phenolic odor. (NTP, 1992)
Crystals from ligroin
Strong phenolic odor
277°C(lit.)
120°C/39mmHg(lit.)
Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
82°C(lit.)
no data available
no data available
Moderately acidic substance
no data available
less than 0.1 mg/mL at 64° F (NTP, 1992)
log Kow = 3.69
1 mm Hg ( 76.5 °C)
1.49
no data available
no data available
Decomposes on heating. This produces toxic and corrosive fumes including hydrogen chloride and chlorine. Reacts with strong oxidants.
Stable up to its melting point
Non-combustible /Trichlorophenol/2,4,6-TRICHLOROPHENOL is incompatible with acid chlorides, acid anhydrides and oxidizing agents. It can be converted to the sodium salt by reaction with sodium carbonate. Forms ethers, esters and salts by reaction with metals and amines. Undergoes substitution reactions such as nitration, alkylation, acetylation and halogenation. Can be hydrolyzed by reaction with bases at elevated temperatures and pressures. Reacts with alkalis at high temperatures (NTP, 1992).
no data available
Incompatible materials: Strong oxidizing agents.
When heated to decomposition it emits toxic fumes of /hydrogen chloride/.
no data available
no data available
no data available
no data available
CLASSIFICATION: B2; probable human carcinogen. BASIS FOR CLASSIFICATION: Based on no human data and sufficient evidence in animals; namely, increased incidence of lymphomas or leukemia in male rats and hepatocellular adenomas or carcinomas in male and female mice. HUMAN CARCINOGENICITY DATA: None. ANIMAL CARCINOGENICITY DATA: Sufficient.
No studies are available on the developmental or reproductive effects of 2,4,6-trichlorophenol in humans from inhalation or oral exposure. Animal studies have reported a transient reduction in the body weight of the offspring of rats exposed to 2,4,6-trichlorophenol orally, while no other developmental effects have been noted in animal studies. Reduced mean litter size was observed in rats following maternal exposure to 2,4,6-trichlorophenol in the drinking water, while no reproductive effects were observed in other animal studies via gavage (placing the chemical experimentally in the stomach).
The substance is severely irritating to the eyes, skin and respiratory tract.
Repeated or prolonged contact with skin may cause dermatitis including chloracne. The substance may have effects on the liver. This may result in impaired functions.
No indication can be given about the rate at which a harmful concentration of this substance in the air is reached when dispersed.
AEROBIC: 2,4,6-Trichlorophenol biodegraded 100% in 10-14 days with an 8 day lag time in filtered water and in 8-10 days with a 2 day lag time in water with sediment(1). 2,4,6-Trichlorophenol is expected to biodegrade in aerobic soils with a biodegradation half-life of about 5 days(2). Total degradation of 2,4,6-trichlorophenol in Dunkirk silt loam took 5 days and in Mardin silt loam took 13 days(3). In Labisch soil, 2,4,6-trichlorophenol biodegraded 67% in 60 days(4). 2,4,6-Trichlorophenol was aerobically degraded 95% in 3 days and 27% in 80 days in non-sterile and sterile clay loam, respectively(5). Microbial degradation, volatilization, and photodecomposition were ruled out in the sterile soil indicating that other mechanisms contribute to degradation(5). Activated sludge made from soil resulted in 100% removal of 2,4,6-trichlorophenol in 3 days(6); sewage seed resulted in complete removal in 7 days(7); 39% removal by activated sludge in 14 days was reported(8). 2,4,6-Trichlorophenol was readily degraded in an aerobic microcosm using soils from the saturated zone(9). A 2,4-dichlorophenol-acclimated soil inoculum completely degraded an unspecified initial concentration of 2,4,6-trichlorophenol in 28 days(10). 2,4,6-Trichlorophenol, present at 1.5 mg/L, was completely degraded in 8 days using an inoculum derived from river sediment obtained near a petrochemical plant(11). The compound was 92% degraded in 30 days using an activated sludge inoculum(12). 2,4,6-Trichlorophenol, present at 100 mg/L, reached 82.5-89.3% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(13).
BCFs of 250-310 were reported for Golden Orfe fish (1,2). BCFs of 87 and 676 were reported for flagfish (Jordanella floridae)(3). A BCF of 270 was also reported(4). According to a classification scheme(5), these BCF values suggest that bioconcentration in aquatic organisms is moderate to high(SRC).
The Koc values of 2,4,6-trichlorophenol in soil at pH 6, 7 and 7.7 were measured as 2200, 600 and 150 respectively(1). Koc values of 1300 and 800 were determined in river and lake sediment at an unspecified pH(2). Koc values of 2000(3), 1050(4) and 1070(5) were also reported for 2,4,6-trichlorophenol. According to a classification scheme(6), these Koc values suggest that 2,4,6-trichlorophenol is expected to have moderate to slight mobility in soil. The pKa of 2,4,6-trichlorophenol is 6.23(7), indicating that this compound will exist partially in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(8).
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: UN2020 (For reference only, please check.)
IMDG: UN2020 (For reference only, please check.)
IATA: UN2020 (For reference only, please check.)
ADR/RID: CHLOROPHENOLS, SOLID (For reference only, please check.)
IMDG: CHLOROPHENOLS, SOLID (For reference only, please check.)
IATA: CHLOROPHENOLS, SOLID (For reference only, please check.)
ADR/RID: 6.1 (For reference only, please check.)
IMDG: 6.1 (For reference only, please check.)
IATA: 6.1 (For reference only, please check.)
ADR/RID: III (For reference only, please check.)
IMDG: III (For reference only, please check.)
IATA: III (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Some technical products may contain highly toxic impurities including polychlorinated dibenzo-p-dioxins and furans.See ICSCs 0588, 0589, 0590 and 879.