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Пентахлорфенол

Пентахлорфенол структура
87-86-5
CAS №
87-86-5
Химическое название:
Пентахлорфенол
английское имя:
Pentachlorophenol
Синонимы:
dust;PCP;Penta;2,3,4,5,6-Pentachlorophenol;Pentachlorphenol;mist;hog;good;Chlorophen;Phenol, pentachloro-
CBNumber:
CB8854526
Формула:
C6HCl5O
молекулярный вес:
266.34
MOL File:
87-86-5.mol

Пентахлорфенол атрибут

Температура плавления: 165-180 °C(lit.)
Температура кипения: 310 °C(lit.)
плотность: 1.978 g/mL at 25 °C(lit.)
плотность пара: 9.2 (vs air)
давление пара: 40 mm Hg ( 211.2 °C)
показатель преломления: 1.6310 (estimate)
Fp: 11 °C
температура хранения: 0-6°C
растворимость: Chloroform (Slightly), Ethyl Acetate (Sparingly)
пка: 4.80 (Blackman et al., 1955)
5.3 (Eder and Weber, 1980)
Растворимость в воде: 80 mg l-1(30 °C)
форма: жидкость
Удельный вес: 1.979
Мерк: 7109
БРН: 1285380
констант закона Генри: 21 (quoted, Petrasek et al., 1983)
Пределы воздействия: NIOSH REL: IDLH 0.5 mg/m3, IDLH 2.5 mg/m3; OSHA PEL: TWA 0.5 mg/m3; ACGIH TLV: TWA 0.5 mg/m3
Стабильность:: Стабильный. Несовместим с сильными окислителями.
Стандарт первичной питьевой воды EPA: MCL:0.001,MCLG:zero
Непрямые добавки, используемые в веществах, контактирующих с пищевыми продуктами: PENTACHLOROPHENOL
FDA 21 CFR: 175.105
Справочник по базе данных CAS: 87-86-5(CAS DataBase Reference)
Рейтинг продуктов питания EWG: 9
FDA UNII: D9BSU0SE4T
Предложение 65 Список: Pentachlorophenol
МАИР: 1 (Vol. 53, 71, 117) 2019
Система регистрации веществ EPA: Pentachlorophenol (87-86-5)
Пестициды: Закон о свободе информации (FOIA): Pentachlorophenol
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности T+,N,T,F,Xn
Заявления о рисках 24/25-26-36/37/38-40-50/53-39/23/24/25-23/24/25-11-52/53-51/53
Заявления о безопасности 22-36/37-45-52-60-61-16-7
РИДАДР UN 3155 6.1/PG 2
OEB C
OEL TWA: 0.5 mg/m3 [skin]
WGK Германия 3
RTECS SM6300000
Класс опасности 6.1(a)
Группа упаковки II
кода HS 29081100
Банк данных об опасных веществах 87-86-5(Hazardous Substances Data)
Токсичность Pentachlorophenol (PCP) is very toxic to plants and are used as preharvest defoliants and general herbicides. Their use as herbicides is currently restricted to nonagricultural uses along drainage ditches, driveways, and fencerows.
Commercial (technical) grades of PCP commonly contain manufacturing by- products, such as dioxin (HxCDD), which can be more toxic than the PCP itself. Another contaminant in PCP is HCB (Hexachlorobenzene). The use of PCP is being phased out because of the discovery of these highly toxic contaminants (9). PCP is a Restricted Use Pesticide (RUP). Restricted Use Pesticides may be purchased and used only by certified applicators.
In 1988 the EPA announced further restrictions on the use of PCP as in the pulp and paper industry where it is used in paper coatings, sizing, adhesives and in inks. Registration for use in cooling towers and for certain oil well operations was also cancelled. The 1988 regulations also required compliance with dioxin (HxCDD) concentration limits in the final product.
ИДЛА 2.5 mg/m3
символ(GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
сигнальное слово Danger
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H315 При попадании на кожу вызывает раздражение. Разъедание/раздражение кожи Категория 2 Предупреждение GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 При попадании в глаза вызывает выраженное раздражение. Серьезное повреждение/раздражение глаз Категория 2А Предупреждение GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 Может вызывать раздражение верхних дыхательных путей. Специфическая токсичность на орган-мишень, однократное воздействие; Раздражение дыхательных путей Категория 3 Предупреждение GHS hazard pictograms
H351 Предполагается, что данное вещество вызывает раковые заболевания. Канцерогенность Категория 2 Предупреждение P201, P202, P281, P308+P313, P405,P501
H410 Чрезвычайно токсично для водных организмов с долгосрочными последствиями. Опасность для водной среды, долгосрочная опасность Категория 1 Предупреждение GHS hazard pictograms P273, P391, P501
H330 Смертельно при вдыхании. Острая токсичность, ингаляционная Категория 1, 2 Опасность GHS hazard pictograms P260, P271, P284, P304+P340, P310,P320, P403+P233, P405, P501
H301+H311 Токсично при проглатывании или при контакте с кожей.
Внимание
P202 Перед использованием ознакомиться с инструкциями по технике безопасности.
P273 Избегать попадания в окружающую среду.
P280 Использовать перчатки/ средства защиты глаз/ лица.
P302+P352+P312 ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды. Обратиться за медицинской помощью при плохом самочувствии.
P304+P340+P310 ПРИ ВДЫХАНИИ: Свежий воздух, покой. Немедленно обратиться за медицинской помощью.
P305+P351+P338 ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.

Пентахлорфенол химические свойства, назначение, производство

Химические свойства

Pentachlorophenol is a colorless to white, crystalline solid. It has a benzene-like odor; pungent when hot. The Odor Threshold in water is 1600 μg/L and the taste threshold in water is 30 μg/L.

Физические свойства

White flakes or needles with a phenolic odor. At 40 °C, the average odor threshold concentration and the lowest concentration at which an odor was detected were 23 and 9.3 μg/L, respectively. At 25 °C, the lowest concentration at which a taste was detected was 8 μg/L (Young et al., 1996).

Использование

Pentachlorophenol (PCP) is an odourless, white or light brown powder or crystal in appearance. It is used as herbicide and fungicide. Pentachlorophenol is incompatible with strong oxidising agents. Pentachlorophenol has a very sharp characteristic phenolic smell when hot but very little odour at room temperature. Pentachlorophenol is a synthetic substance made from other chemicals and does not occur naturally in the environment. Initially pentachlorophenol was widely used as a wood preservative. It is now used industrially as a wood preservative for power line poles, cross arms, fence post, etc.
Used as insecticide for terminate control; pre-harvest defoliant; general herbicide. Antimicrobial preservative and fungicide for wood, wood products, starches, textiles, paints, adhesives, leather, pulp, paper, industrial waste systems, building materials. Surface disinfectant.

Методы производства

Pentachlorophenol can be produced by the chlorination of phenol in the presence of AlCl3, or by hydrolysis of hexachlorobenzene with NaOH in methanol.

Определение

ChEBI: A chlorophenol that is phenol substituted by 5 chloro groups.

Общее описание

A white crystalline solid. Slightly soluble in water. Noncombustible. Toxic by inhalation, ingestion, and skin absorption. Used as a fungicide and as a wood preservative.

Реакции воздуха и воды

Slightly soluble in water.

Профиль реактивности

Pentachlorophenol may react with strong oxidizing agents. Incompatible with strong bases, acid chlorides and acid anhydrides. Forms salts with alkaline metals. Solutions in oil cause natural rubber to deteriorate, but synthetic rubber may be used in equipment and for protective clothing .

Угроза здоровью

Dust or vapor irritates skin and mucous membranes, causing coughing and sneezing. Ingestion causes loss of appetite, respiratory difficulties, anesthesia, sweating, coma. Overexposure can cause death.

Пожароопасность

Special Hazards of Combustion Products: Generates toxic and irritating vapors.

Сельскохозяйственное использование

Fungicide, Herbicide, Slimicide, Wood preservative: Pentachlorophenol (PCP) is a commercially produced insecticide, fungicide, and slimicide. Since 1984 it has been restricted to certified applicators and is no longer available to the general public. It is primarily used to protect timber from fungal rot and wood-boring insects, but may also be used as a pre-harvest defoliant in cotton, a general pre-emergence herbicide, and as a biocide in industrial water systems. Not approved for use in EU countries. Not registered for use in the U.S. There are 48 global suppliers.

Торговое название

(The U.S. EPA lists 626 active and canceled/ transferredlabelsforthischemical) CHEM-TOL®; CHLON®; CHLOROPHEN®; CRYPTOGIL OL®; DOWCIDE® 7; DOWICIDE® 7; DOW PENTACHLOROPHENOL DP-2 ANTIMICROBIAL®; DURA TREET II®; DUROTOX®; EP 30®; FORPEN-50®; FUNGIFEN®; GLAZDPENTA ®; GRUNDIER ARBEZOL®; LAUXTOL®; LIROPREM®; ONTRACK WE HERBICIDE®; ORTHO TRIOX®; OSMOSE WPC®; PENTACHLOROPHENOL, DOWICIDE EC-7®; PENTACHLOROPHENOL, DP- 2®; PENTACON®; PENTA-KIL®; PENTA READY®; PENTASOL®; PENWAR®; PERATOX®; PERMACIDE®; PERMAGARD®; PERMASAN®; PERMATOX DP- 2®PERMATOX PENTA®; PERMITE®; POL NU®; PREVENTOL P®; PRILTOX®; SANTOBRITE®; SANTOPHEN®; SINITUHO®; TERM-I-TROL®; THOMPSON'S WOOD FIX®; WATERSHED WP®; WEEDONE®; WOODTREAT A®

Профиль безопасности

Confirmed human carcinogen with experimental tumorigenic data. Human poison by ingestion. Poison experimentally by ingestion, skin contact, intraperitoneal, and subcutaneous routes. An experimental teratogen. Other experimental reproductive effects. A skin irritant. Mutation data reported. Acute poisoning is marked by weakness with changes in respiration, blood pressure, and urinary output. Also causes dermatitis, convulsions, and collapse. Chronic exposure can cause liver and hdney injury. Dangerous; when heated to decomposition it emits highly toxic fumes of Cl-. See also CHLOROPHENOLS

Возможный контакт

Pentachlorophenol (PCP) is a commercially produced bactericide, fungicide, and slimicide used primarily for the preservation of wood, wood products; and other materials. As a chlorinated hydrocarbon, its biological properties have also resulted in its use as an herbicide, and molluscicide. Two groups can be expected to encounter the largest exposures. One involves the small number of employees involved in the manufacture of PCP. All of these are presently under industrial health surveillance programs. The second and larger group are the formulators and wood theaters. Exposure, hygiene and industrial health practices can be expected to vary from the small theaters to the larger companies. The principal use as a wood preservative results in both point source water contamination at manufacturing and wood preservation sites and, conceivably, nonpoint source water contamination through runoff wherever there are PCP-treated lumber products exposing PCP to soil

Канцерогенность

The IARC has determined that there is limited evidence for carcinogenicity in humans and sufficient evidence of carcinogenicity in experimental animals.

Экологическая судьба

Biological. Under aerobic conditions, microbes in estuarine water partially dechlorinated pentachlorophenol to trichlorophenol (Hwang et al., 1986). The disappearance of
pentachlorophenol was studied in four aquaria with and without mud under aerobic and anaerobic conditions. Potential biological and/or chemical products identified include pentachloroanisole, 2,3,4,5-, 2,3,4,6- and 2,3,5,6-tetrachlorophenol (Boyle et al.,
Pentachlorophenol degraded in anaerobic sludge to 3,4,5-trichlorophenol which was further reduced to 3,5-dichlorophenol (Mikesell and Boyd, 1985). In activated sludge, only 0.2% of the applied amount was mineralized to carbon dioxide after 5 days (Freitag
Pentachlorophenol was statically incubated in the dark at 25°C with yeast extract and settled domestic wastewater inoculum. Significant biooxidation was observed but with a gradual adaptation over a 14-day period to achieve complete degradation at 5 mg/L substrate cultures. At a concentration of 10 mg/L, it took 28 days for pentachlorophenol to degrade completely (Tabak et al., 1981).
Melcer and Bedford (1988) studied the fate of pentachlorophenol in municipal activated sludge reactor systems that were operated at solids retention times of 10 to 20 days and hydraulic retention times of 120 days. Under these conditions, pentachloropheno

Метаболизм

Pentachlorophenol was metabolized in rats by conjugation with glucuronic acid and eliminated as the glucuronide. P450 catalyzed oxidative dechlorination also occurred to form tetrachlorohydroquinone, and this was conjugated to form a monoglucuronide representing 27% of the dose administered. Other metabolites have been reported, including isomeric tetrachlorophenols, tetrachlorocatechol and tetrachlororesorcinol. Trace amounts of benzoquinones were also noted. Metabolites in female rats were tetrachloromonophenols, diphenols, and hydroquinones.

Перевозки

UN3155 Pentachlorophenol, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Методы очистки

Crystallise it twice from toluene/EtOH. Sublime it in vacuo.[Beilstein 6 IV 1025.]

Несовместимости

Reacts violently with strong oxidizers, acids, alkalies, and water.

Утилизация отходов

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and 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. Incineration (600°to 900°C) coupled with acequate scrubbing and ash disposal facilities. Alternatively pentachlorophenol

Пентахлорфенол препаратная продукция и сырье

сырьё

препарат

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