12698-64-5Oc1c(Cl)cc(Cl)c(Cl)c1ClVGVRPFIJEJYOFN-UHFFFAOYSA-N2,3,4,6-tetrachlorophenol appears as brown flakes or beige solid. Strong odor. (NTP, 1992)
12698-64-5、58-90-2DTXSID9021716CHEMBL320361CHEBI:132359Other Classes -> Chlorophenols
Other Classes -> Chlorophenols
Carcinogens
Chlorinated/Brominated phenol
log Kow= 4.45
4.45
4.3
1.839 at 77 °F (NTP, 1992) - Denser than water; will sink
1.839 @ 25 °C/4 °C
1.8 g/cm³
NEEDLES FROM LIGROIN, ACETIC ACID
BROWN FLAKES OR SUBLIMED MASS
LIGHT BROWN MASS
less than 1 mg/mL at 68 °F (NTP, 1992)
SLIGHTLY SOL IN HOT WATER; VERY SOL IN SODIUM HYDROXIDE; SOL IN HOT ACETIC ACID.
SOL IN ACETONE.
In water, 0.10 g/100 g water (temperature not specified).
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
Danger
H301: Toxic if swallowed [Danger Acute toxicity, oral]
P264, P264+P265, P270, P273, P280, P301+P316, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, P391, P405, and P501 (click each P-code to see the statement)
Danger
H301+H311 (88.6%): Toxic if swallowed or in contact with skin [Danger Acute toxicity, oral; acute toxicity, dermal]
P262, P264, P264+P265, P270, P273, P280, P301+P316, P302+P352, P305+P351+P338, P316, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P391, P405, and P501 (click each P-code to see the statement)
Hazard Traits - Neurotoxicity
The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)
Literature sources indicate that this compound is nonflammable. (NTP, 1992)
· Combustible material: may burn but does not ignite readily.
· Combustible material: may burn but does not ignite readily.
Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
SYMPTOMS: Symptoms of exposure to this compound may include irritation of the skin, eyes, nose, and pharynx; conjunctivitis, corneal injuries, and dermatitis with repeated skin contact. Symptoms of exposure to phenols (through ingestion or contact with the skin or mucous membranes) may include painless blanching or erythema, possible corrosion, profuse sweating, intense thirst, nausea and vomiting, diarrhea, cyanosis from methemoglobinemia, hyperactivity; stupor; blood pressure fall; hyperpnea; abdominal pain; hemolysis; convulsions; coma; and pulmonary edema followed by pneumonia. If death from respiratory failure is not immediate, jaundice and oliguria or anuria may occur. Skin sensitivity occasionally occurs.
CHLORINATED PHENOLS ... ARE VERY EFFECTIVE (... IN VITRO) AS UNCOUPLERS OF OXIDATIVE PHOSPHORYLATION. THEY THUS PREVENT INCORPORATION OF INORGANIC PHOSPHATE INTO ATP WITHOUT AFFECTING ELECTRON TRANSPORT. AS A RESULT OF THIS ACTION, WHICH IS BELIEVED TO OCCUR @ MITOCHONDRIAL /MEMBRANE/, CELLS CONTINUE TO RESPIRE BUT SOON ARE DEPLETED OF ATP NECESSARY FOR GROWTH. /CHLOROPHENOLS/
The chlorophenols ... act at the sites of adenosine triphosphate production and decrease or block it without blocking the electron transport chain. Thus the poisons uncouple phosphorylation from oxidation. Free energy from the electron transport chain then converts to more body heat. As body temp rises, heat-dissipating mechanisms are overcome and metabolism is speeded. More adenosine diphosphate and other substrates accumulate, and these substrates stimulate the electron transport chain further. The electron transport chain responds by using up more and more available oxygen (increasing oxygen demand) in an effort to produce adenosine triphosphate but much of the free energy generated is liberated as still more body heat. Oxygen demand quickly overcomes oxygen supply, and energy reserves become depleted. /Chlorophenols/
... IN MALE WISTAR RATS, FED BY STOMACH TUBE 8 MG OF /HEXACHLOROBENZENE/ ... PER KG (IN SUNFLOWER OIL) FOR 19 DAYS ... URINE CONTAINED ... PENTACHLOROPHENOL, WHICH WAS ... SOMETIMES ASSOCIATED WITH 2,3,4,6-TETRACHLOROPHENOL ... .
URINE & ORGANS OF RATS WERE EXAMINED FOR METABOLITES AFTER ORAL DOSAGE OF BETA-(BENZENE HEXACHLORIDE) (BHC). BETA-(BENZENE HEXACHLORIDE) WAS CONVERTED TO 2,3,4,6-TETRACHLOROPHENOL & OTHER CHLOROPHENOLS.
LINDANE WAS METABOLIZED BY HUMAN & RAT LIVER MICROSOMES TO SEVERAL METABOLITES, INCLUDING 2,3,4,6-TETRACHLOROPHENOL.
MALE & FEMALE RATS WERE GIVEN ORALLY WITHIN 1 MONTH 770 MG/KG HEXACHLOROBENZENE, & 2,3,4,6-TETRACHLOROPHENOL WAS FOUND AS A METABOLITE IN KIDNEY, SPLEEN, & HEART SAMPLES.
For more Metabolism/Metabolites (Complete) data for 2,3,4,6-TETRACHLOROPHENOL (6 total), please visit the HSDB record page.
불러오는 중…
Sol in ethanol, benzene, chloroform.
Solubility in water, g/100ml at 20 °C: 0.1 (very poor)
302 °F at 15 mmHg (NTP, 1992)
64 °C (3.0 kPa)
· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.
· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.
A nose, throat, and respiratory tract irritant; [HSDB] Prolonged contact corrosive to eyes; May cause skin burns, hyperthermia, methemoglobinemia, liver and kidney damage, and convulsions; [CAMEO] A skin, eye, and respiratory tract irritant; May cause liver injury and chloracne; [ICSC] A severe skin and eye irritant; A mucous membrane and upper respiratory tract irritant; May cause liver damage; Effects in high-dose animal studies include convulsions or effect on seizure threshold; [MSDSonline] See CHLOROPHENOLS.
May be contaminated with dioxins and furans; Higher chlorinated compounds, e.g., tri-, tetra-, and pentachlorophenols are less likely to cause seizures and more likely to cause hyperthermia (uncoupling of oxidative phosphorylation); Lower chlorinated compounds, e.g., dichlorophenols, less likely to cause hyperthermia and more likely to cause seizures; Lower chlorinated phenols (all except pentachlorophenol) cause chemical burns on prolonged contact; Skin exposure can be lethal, e.g., 2,4-dichlorophenol to just 10% of body surface area; Other toxic effects in poisoning causes include metabolic acidosis and injury to the liver and kidneys; [HSDB] High doses may cause convulsions and injury to the liver and kidneys; Tetra- and pentachlorophenols can cause uncoupling of oxidative phosphorylation; [Ullmann] Pentachlorophenol does not appear to be a primary neurotoxin; [Sullivan, p. 1257] Pentachlorophenol is 40 times more toxic as an uncoupler than 2,4-dichlorophenol; Commercial mono- and dichlorophenols contain little or no detectable dioxins or furans; What we know of human effects are based primarily on studies of workers in chemical manufacturing (dichlorophenols and trichlorophenols) and wood-preservation applicators (trichlorophenols, tetrachlorophenols, and pentachlorophenol); MCPs, DCPs, and 2,4,6-T3CP are convulsive agents; The other T3CPs and T4CPs are not; All of the chlorophenols are irritating or corrosive to the skin; The dioxins and furans that contaminate tri-, tetra-, and pentachlorophenol are probably the causal agents of chloracne; [Reference #1] Combined exposures to polychlorophenols or to their sodium salts are possibly carcinogenic to humans (Group 2B). [IARC]
2020 153
2021 153
F027; Discarded unused formulations containing tri-, tetra-, or pentachlorophenol or discarded unused formulations containing compounds derived from these chlorophenols are classified as a hazardous waste from a nonspecific source and must be managed according to Federal and/or State hazardous waste regulations. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (see 40 CFR 261.5).
2,3,4,6-TETRACHLOROPHENOL reacts as a weak organic acid and is incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. May generate heat with bases. Such heating may initiate polymerization.
Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
Use water spray, alcohol-resistant foam, dry powder, carbon dioxide.
Fresh air, rest. Refer for medical attention.
Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Give a slurry of activated charcoal in water to drink. Refer for medical attention .
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.
· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
General First Aid:
General First Aid:
· Wear positive pressure self-contained breathing apparatus (SCBA).
· Wear positive pressure self-contained breathing apparatus (SCBA).
MATERIALS WHICH ARE TOXIC AS STORED OR WHICH CAN DECOMPOSE INTO TOXIC COMPONENTS ... SHOULD BE STORED IN A COOL WELL VENTILATED PLACE, OUT THE DIRECT RAYS OF THE SUN, AWAY FROM AREAS OF HIGH FIRE HAZARD, AND SHOULD BE PERIODICALLY INSPECTED ... INCOMPATIBLE MATERIALS SHOULD BE ISOLATED ...
SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
SRP: Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area. Ventilation control of the contaminant as close to its point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants.
Excerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Immediate precautionary measure
Immediate precautionary measure
44 adipose and 13 liver samples were taken from 58 people from the southern and northern parts of Finland. Donors ranged from 3 mo to 91 yr, and none were known to be occupationally exposed. Upon tissue analysis, only very small residues of chlorophenols were found (in 61% of the samples). The median concn of 2,3,4,6-tetrachlorophenol in adipose tissue samples was 0.002 ug/g fat, ranging from a trace amount (0.001 ug/g) to 0.031 ug/g. Only 2 liver samples were positive for tetrachlorophenol (0.002 and 0.007 ug/g). Both liver and adipose samples were obtained from the same donor only once. In this case tetrachlorophenol concn in adipose tissue was 0.003 ug/g fat, while in the liver no detectable amount was found. The age, smoking habit or fish intake of the donor did not have any relation to the chlorophenol concn found in the tissue sample.
Mean 2,3,4,6-tetrachlorophenol concns in adipose tissue samples of hospital patients from Helsinki, Tammisaari, and Kemi, Finland were 0.004, 0.004, and 0.006 ug/g residue fat, respectively(1). The mean 2,3,4,6-tetrachlorophenol concn in the adipose tissue of cadavers from the province of Uusimaa in Southern Finland was 0.005 ug/g residue fat(1). 2,3,4,6-Tetrachlorophenol was detected in the liver tissue of 2 of 13 cadavers from the province of Uusimaa in southern Finland at concns of 0.002 and 0.007 ug/g(1). 2,3,4,6-Tetrachlorophenol was detected in serum of Finnish sawmill workers, following exposure to sodium chlorophenolate, at mean concns of 2.79 and 2.78 umol/l before and after working hours, respectively(2). The mean concn of 2,3,4,6-tetrachlorophenol in the urine of Finnish sawmill workers during lumber treatment was 7.59 umol/l(2). 2,3,4,6-Tetrachlorophenol was detected in the urine of exposed Finnish sawmill workers from 2 of 3 sawmills at concns ranging from 5.1 to 14.9 ng/mg creatinine; it was detected in 2 non-exposed controls at concns of 1.1 and 8.6 ng/mg creatinine(3). 2,3,4,6-Tetrachlorophenol was detected in the urine of exposed workers in a Canadian pressure treatment plant at a mean concn of 0.11 mg/l and in the urine of Finnish sawmill workers at a mean concn of 1 mg/l, range <0.2 to 10 mg/l(4).
LC50 Carassius auratus (goldfish) 0.75 ppm/24 hr /Conditions of bioassay not specified/
LC50 Rivulus marmoratus 1.10 mg/l 96 hr /Conditions of bioassay not specified/
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 6300(SRC), determined from a log Kow of 4.45(2) and a regression-derived equation(3), indicates that 2,3,4,6-tetrachlorophenol is expected to be immobile in soil(SRC). Volatilization of 2,3,4,6-tetrachlorophenol from moist soil surfaces may be important(SRC) given an estimated Henry's Law constant of 1.3X10-6 atm-cu m/mole(SRC), derived from its vapor pressure(4) and water solubility(5). However, 2,3,4,6-tetrachlorophenol's pKa of 5.22(6) suggests this process may be attenuated under environmental pHs(SRC). 2,3,4,6-Tetrachlorophenol is not expected to volatilize from dry soil surfaces based on a vapor pressure of 4.23X10-3 mm Hg(4). 2,3,4,6-Tetrachlorophenol persisted for >72 days in a laboratory test with a soil inoculum(7). Another study reported that 2,3,4,6-tetrachlorophenol disappeared from soil to a large degree in 4 weeks(8).
AQUATIC FATE: Based on a classification scheme(1), Koc values ranging from 6040 to 7690 in river sediment, lake sediment and aquifer material(2), indicate that 2,3,4,6-tetrachlorophenol is expected to adsorb to suspended solids and sediment in water(SRC). 2,3,4,6-Tetrachlorophenol is expected to volatilize slowly from water surfaces(3,SRC) based on an estimated Henry's Law constant of 1.3X10-6 atm-cu m/mole(SRC), derived from its vapor pressure of 4.23X10-3 mm Hg at 25 °C(4) and water solubility of 1000 mg/l(5). Estimated volatilization half-lives for a model river and model lake are 43 and 320 days, respectively(3,SRC). However, a pKa of 5.22 for 2,3,4,6-tetrachlorophenol(6) indicates that 2,3,4,6-tetrachlorophenol will not significantly volatilize from water as it will exist predominately in the ionic form under environmental pHs(SRC). According to a classification scheme(7), BCFs ranging from 25 to 200(8,9), suggest that bioconcentration in aquatic organisms is low to high(SRC). 51% (89%) disappearance of 2,3,4,6-tetrachlorophenol was observed following 6 (24) hours irradiation (> or = 285 nm) in a 1:1 (v/v) water:acetonitrile mixture; 2,3,4-and 2,3,6-trichlorophenol were identified as photoproducts in the n-hexane extracts when the pH was changed to <1(10). 2,3,4,6-Tetrachlorophenol, concn 100 mg/l, reached 7% of its theoretical BOD over 4 weeks using an activated sludge inoculum(9). High-rate operation of an aerobic fluidized-bed reactor resulted in a 99.6% mean removal of 2,3,4,6-tetrachlorophenol over a period of 235 days(11). 74% removal of 2,3,4,6-tetrachlorophenol was observed after 32 days anaerobic incubation in mixed digested sludge(12).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 2,3,4,6-tetrachlorophenol, which has a vapor pressure of 4.23X10-3 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 2,3,4,6-tetrachlorophenol is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 58 days(3,SRC).
Although no data on 2,3,4,6-tetrachlorophenol could be located, the presence of pentachlorophenol in 1-3% of market basket surveys (and an estimated daily intake of 1-6 ug/day)(1) combined with the fact that tetrachlorophenol is a major impurity in commercial pentachlorophenol(4-10%) would lead to the speculation that residues of 2,3,4,6-tetrachlorophenol are in food which contains residues of pentachlorophenol.
Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Neurotoxin - Other CNS neurotoxin
Earthworms collected 5, 7, and 10 m from the dipping basin of a sawmill near the town of Kuopio in central Finland contained 2,3,4,6-tetrachlorophenol at concns of 430 (1980), 390 (710), and 380 (270) ug/g fat for Lumbricus spp (A. caliginosa), respectively(1).
Cough. Shortness of breath. Convulsions.
MAY BE ABSORBED! Redness.
Redness. Pain.
Abdominal pain. Diarrhoea. Headache. Dizziness. Vomiting. Weakness. Convulsions. Muscle spasms. Fever. Sweating.
Final effluent from the Hogsmill Valley municipal treatment works, London, contained 63 parts per trillion 2,3,4,6-tetrachlorophenol(1). It was detected, not quantified, in chemical and sewage treatment plant effluent in Chattanooga Creek, Chattanooga, TN(2). Mean 2,3,4,6-tetrachlorophenol concns in the effluent (influent) of six municipal wastewater treatment plants in the Netherlands were, ug/l: trickling filter, 0.06 (0.11), 0.10 (0.14); activated sludge, 0.11 (0.13), 0.18 (0.19); and oxidation ditch, 0.21 (0.25), and 0.06 (0.16)(3). 2,3,4,6-Tetrachlorophenol was detected in the effluent (influent) of a Swiss wastewater treatment plant at an average concn of 4.9 (7.3) ug/l(4). Treated pulp mill effluent contained 1.1 ug/l tetrachlorophenol(5). 2,3,4,6-Tetrachlorophenol concns in the effluent water after the bleaching of pulp were 7.5 and 9.8 ug/l on Mar 16 and Nov 3, 1983, respectively(6). 2,3,4,6-Tetrachlorophenol was detected in waste liquors of pine kraft pulp bleaching stages C and E at concns of 2.88 and 43.7 ug/l, respectively; 2.72 and 45.4 ug/l, respectively, were detected in the waste liquors in a chemically-bound form(7). Water samples collected within a sawmill using a chlorophenol wood preservative contained 2,3,4,6-tetrachlorophenol at concns ranging from 0.66 to 79.30 ug/l and 12.40 to 179.00 ug/l in surface water and groundwater, respectively; samples of water taken from a blind drain 1 m from the dipping basin contained 14,300 ug/l 2,3,4,6-tetrachlorophenol(8). Waste liquors from two kraft pulp mills and one sulfite pulp mills in Central Finland contained 2,3,4,6-tetrachlorophenol at concns of 10, 7 and 1 ug/l, respectively(9).
2,3,4,6-Tetrachlorophenol
Hepatic
3 x 10 ^-2 mg/kg-day
F027; Discarded unused formulations containing tri-, tetra-, or pentachlorophenol or discarded unused formulations containing compounds derived from these chlorophenols are classified as a hazardous waste from a nonspecific source and must be managed according to Federal and/or State hazardous waste regulations. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (see 40 CFR 261.5).
This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Chlorophenols is produced, as an intermediate or final product, by process units covered under this subpart. /Chlorophenols/
Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 10 lb or 4.54 kg. The toll free number of the NRC is (800) 424-8802; In the Washington D.C. metropolitan area (202) 426-2675. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).
(FL) FLORIDA 210 ug/l
(NH) NEW HAMPSHIRE 200 ug/l
The compounds are readily absorbed from the gastroenteric tract and from parenteral sites of injection. /Chlorophenols/
UNLIKE AQ SUSPENSIONS, TETRACHLOROPHENOL DISSOLVED IN ORGANIC SOLVENTS MAY BE ABSORBED THROUGH THE SKIN IN ACUTELY TOXIC AMOUNTS. /TETRACHLOROPHENOL/
AFTER IP ADMIN (4.9 MG) IN RATS, 95.9% 2,3,4,6-TETRACHLOROPHENOL WAS ELIMINATED IN URINE WITHIN 48 HR.
AFTER INTRAGASTRIC DOSES OF 0, 300, 360, 410, 432, 518, & 632 MG/KG IN WISTAR RATS, THE HIGHEST TCP RESIDUES WERE FOUND IN THE SPLEEN (146 MG/KG), FOLLOWED BY KIDNEY (47 MG/KG) & LIVER (34 MG/KG). AFTER INTRAGASTRIC DOSES WITH 0, 10, 50, OR 100 MG/KG/7 DAYS/WK FOR 55 DAYS, THE HIGHEST TCP RESIDUE LEVELS WERE FOUND IN THE SPLEEN & KIDNEY.
For more Absorption, Distribution and Excretion (Complete) data for 2,3,4,6-TETRACHLOROPHENOL (9 total), please visit the HSDB record page.
Used as a pesticide and fungicide; as a slimicide for paper mills; as a preservative; as a component in pentachlorophenol wood preservative; Discontinued by the DOW Chemical Co.; No longer commercially produced in the US; Pure 2,3,4,6-tetrachlorophenol is not sold commercially because of the difficulty encountered in adjusting the chlorination at the tetra stage. It is found in combination with pentachlorophenol. [HSDB]
Pulp and Paper Processing [Category: Industry]
Used as antimicrobials (biocides, fungicides, insecticides, ovicides, algicides) and herbicides; Used as preservatives for wood, glue, paint, vegetable fibers, leather, and furs; Also used to make pharmaceuticals and dyes; [Ullmann] Used in pressure-treatment of wood and in surface treatment of logs, railroad ties, telephone poles, and lumber; Lower chlorophenols were used to make pesticides such as 2,4,5-T; Released into the environment from chlorine bleaching in pulp and paper manufacturing, water treatment, and municipal waste incineration; [Reference #1]
PESTICIDE /FORMER/
SLIMICIDE FOR PAPER MILLS /FORMER/
PRESERVATIVE; COMPONENT IN PENTACHLOROPHENOL WOOD PRESERVATIVE /FORMER/
... Commercial grade 2,3,4,6-tetrachlorophenol contained chlorodioxin isomers at levels of 28 ppm (hexa-), 80 ppm (hepta-), and 30 ppm (octachlorodibenzo-p-dioxin) as well as chlorodibenzofurans at levels of 55 ppm (hexa-), 100 ppm (hepta-), and 25 ppm (octachlorodibenzofuran).
Pentachlorophenol is an impurity in technical grade formulations of tetrachlorophenol.
(1976) 1.8X10+9 g
(1982) NOT PRODUCED COMMERCIALLY IN USA
CHLORINATION OF PHENOL IN THE PRESENCE OF POTASSIUM TELLURATE AS A CATALYST, FOLLOWED BY SEPARATION OF ISOMERIC MIXT; BY PRODUCT FROM PRODUCTION OF PENTACHLOROPHENOL BY CHLORINATION OF PHENOL.
The tri- and tetrachlorophenols produced by direct chlorination of phenol have essentially similar chlorophenol contaminants, varying in concentrations with source and batch. /Tetrachlorophenols/
The commercial tetrachlorophenol was composed of 73% tetra- and 27% pentachlorophenol. /Tetrachlorophenol/
Commercial pentachlorophenol contains 4-10% tetrachlorophenol.
Phenol, 2,3,4,6-tetrachloro-: ACTIVE
PRODUCT DISCONTINUED BY THE DOW CHEMICAL CO.
The isomers are separated from one another via gradient elution with ion-exchange resins.
Pure 2,3,4,6-tetrachlorophenol is not sold commercially because of the difficulty encountered in adjusting the chlorination at the tetra stage. It is found in combination with pentachlorophenol.