Хлорбензол химические свойства, назначение, производство
Химические свойства
Chlorobenzene, also known as monochlorobenzene or MCB, is a colourless flammable liquid with an aromatic almond-like odor, Chlorination of benzene in the presence of a catalyst (FeCl3 or AICI3) yields chlorobenzene as the first product. It is insoluble in water and miscible with organic solvents. Chlorobenzene has a good solvency for fats, oils, resins, polymers, binders, rubber, and chlorinated rubber. Cellulose ethers dissolve in the presence of small amounts of alcohols; cellulose nitrate is insoluble. Chlorobenzene is a solvent in the production of bitumen and asphalt coatings for building protection.
Физические свойства
Clear, colorless, flammable liquid with a sweet almond, medicinal or mothball-like odor. An odor threshold concentration of 210 ppbv was reported by Leonardos et al. (1969). At 40 °C, the lowest concentration at which an odor was detected was 190 μg/L. At 25 °C, the lowest concentration at which a taste was detected was 190 μg/L (Young et al., 1996). The average least detectable odor threshold concentration in water at 60 °C was 0.08 mg/L (Alexander et al., 1982). Cometto-Muiz and Cain (1994) reported an average nasal pungency threshold concentration of 10,553 ppmv. Chlorobenzene can evaporate when exposed to air. It dissolves slightly when mixed with water. It is moderately soluble in water; up to 1,000 milligrams will mix with a liter of water. Chlorobenzene is slightly persistent in water, with a half-life of between 2 to 20 days. It persists in soil (several months), in air (3.5 days), and water (less than 1 day).
Использование
Chlorobenzene is a halogenated benzene that is used as a solvent for paints, as a heat transfer medium, and in the manufacture of phenol, aniline and nitrochlorobenzenes. Now chlorobenzene is mainly used as a solvent for pesticide formulations, diisocyanate manufacture, degreasing automobile parts, and for the production of nitrochlorobenzene and chemical toxicity QSAR research for agricultural pollution.
Определение
ChEBI: Chlorobenzene is the simplest member of the class of monochlorobenzenes, that is benzene in which a single hydrogen has been substituted by a chlorine. It has a role as a solvent.
Подготовка
Chlorobenzene is produced by chlorination of benzene in the presence of a catalyst, and is produced as an end product in the reductive chlorination of di- and trichlorobenzenes.
Общее описание
Chlorobenzene is a colorless to clear, yellowish liquid with a sweet almond-like odor. Flash point 84°F. Practically insoluble in water and somewhat denser than water (9.2 lb / gal). Vapors heavier than air. It can be converted to phenol by reaction with sodium hydroxide under extreme conditions (300°C and 200 atmospheres pressure). Used to make pesticides, dyes, and other chemicals.
Реакции воздуха и воды
Highly flammable. Insoluble in water.
Профиль реактивности
Chlorobenzene undergoes a sometimes explosive reaction with powdered sodium or phosphorus trichloride + sodium. May react violently with dimethyl sulfoxide. Reacts vigorously with oxidizing agents. Attacks some forms of plastic, rubber and coatings. Forms a shock sensitive solvated salt with silver perchlorate.
Опасность
A possible carcinogen. Avoid inhalation
and skin contact. Moderate fire risk. Explosive limits 1.8–9.6%.
Угроза здоровью
Irritating to skin, eyes and mucous membranes. Repeated exposure of skin may cause dermatitis due to defatting action. Chronic inhalation of vapors or mist may result in damage to lungs, liver, and kidneys. Acute vapor exposures can cause symptoms ranging from coughing to transient anesthesia and central nervous system depression.
Limited information is available on the acute (short-term) effects of chlorobenzene. Acute inhalation exposure of animals to chlorobenzene produced narcosis, restlessness, tremors, and muscle spasms. Chronic (long-term) exposure of humans to chlorobenzene affects the central nervous system (CNS). Signs of neurotoxicity in humans include numbness, cyanosis, hyperesthesia (increased sensation), and muscle spasms. No information is available on the carcinogenic effects of chlorobenzene in humans. EPA has classified chlorobenzene as a Group D, not classifiable as to human carcinogenicity.
Пожароопасность
Flammable liquid; flash point (closed cup) 29°C (84°F); vapor pressure 8.8 torr at 20°C (68°F); autoignition temperature 638°C (1180°F). When heated to decomposition this compound emits toxic fumes of hydrogen chloride gas, CO and CO2.
Chlorobenzene vapors form explosive mixtures with air within the range 1.3-7.1% by volume in air. It is incompatible with strong oxidizing agents and dimethyl sulfoxide. Dimethyl sulfoxide decom poses violently in contact with chloroben zene (NFPA 1997). Many metal perchlorates, such as those of silver and mercury, may form shock-sensitive solvated perchlorates that may explode on impact.
Профиль безопасности
Suspected carcinogen.
Moderately toxic by ingestion and
intraperitoneal routes. Experimental
teratogenic and reproductive effects.
Mutation data reported. Strong narcotic with
slight irritant qualities. Dichlorobenzols are
strongly narcotic. Little is known of the
effects of repeated exposures at lower
concentrations, but it may cause hdney and
liver damage. The industrial illnesses
reported may possibly be due to
nitrobenzol. Dangerous fire hazard when
exposed to heat or flame. Moderate
explosion hazard when exposed to heat or
flame. Potentially explosive reaction with
powdered sodium or phosphorus trichloride
+ sodtum. Violent reaction with AgClO4.
Reacts vigorously with oxidizers. See also
CHLORINATED HYDROCARBONS,
AROMATIC. To fight fire, use foam, CO2,
dry chemical, water to blanket fire.
Associated with EPA Superfund sites
Возможный контакт
Chlorobenzene is used in the manufacture of aniline, phenol, and chloronitrobenzene; as an intermediate in the manufacture of dyestuffs and many
pesticides, as a solvent; and emulsifier.
Канцерогенность
Chlorobenzene was not mutagenic in a
variety of bacterial and yeast assays. Existing
data suggest that genotoxicity may not be an
area of concern for chlorobenzene exposure in
humans.
Экологическая судьба
Chlorobenzene's production and use as a chemical intermediate, solvent, and heat transfer medium may result in its release to the environment through various waste streams. If released to air, chlorobenzene will exist solely as a vapor in the atmosphere. Photochemically produced hydroxyl radicals will ultimately degrade vapor-phase chlorobenzene in less than 24h.
Biological. In activated sludge, 31.5% of the applied chlorobenzene mineralized to carbon dioxide after 5 d (Freitag et al., 1985). A mixed culture of soil bacteria or a Pseudomonas sp. transformed chlorobenzene to chlorophenol (Ballschiter and Scholz, 1980). Pure microbial cultures isolated from soil hydroxylated chlorobenzene to 2- and 4-chlorophenol (Smith and Rosazza, 1974). Chlorobenzene was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum. At a concentration of 5 mg/L, biodegradation yields at the end of 1 and 2 wk were 89 and 100%, respectively. At a concentration of 10 mg/L, significant degradation with gradual adaptation was observed.Complete degradation was not observed until after the 3rd week of incubation (Tabak et al.,1981).
https://www.epa.govПеревозки
UN1134 Chlorobenzene, Hazard Class: 3;
Labels: 3-Flammable liquid.
Методы очистки
The main impurities are likely to be chlorinated impurities originally present in the *benzene used in the synthesis of chlorobenzene, and also unchlorinated hydrocarbons. A common purification procedure is to wash it several times with conc H2SO4 then with aqueous NaHCO3 or Na2CO3, and water, followed by drying with CaCl2, K2CO3 or CaSO4, then with P2O5, and distilling. It can also be dried with Linde 4A molecular sieve. Passage through, and storage over, activated alumina has been used to obtain low conductance material. [Flaherty & Stern J Am Chem Soc 80 1034 1958, Beilstein 5 H 199, 5 IV 640.]
Несовместимости
Reacts violently with strong oxidizers;
dimethyl sulfoxide; sodium powder; silver perchlorate;
causing fire and explosion hazard. Attacks some plastics,
rubber, and coatings. Decomposes on heating, producing
phosgene and hydrogen chloride fumes.
Утилизация отходов
Incineration, preferably after
mixing with another combustible fuel; care must be exercised to assure complete combustion to prevent the formation of phosgene; an acid scrubber is necessary to remove
the halo acids produced.
Хлорбензол препаратная продукция и сырье
сырьё
препарат
2-THENOYLACETONITRILE
NAPHTHOL AS-LT
ЭТИЛ-АЛЬФА-ХЛОРОФЕНИЛАЦЕТАТ
2-TERT-BUTYLPYRIDINE-4-CARBONITRILE
DICLOMEZINE
2-Бром-5-нитроимидазола
2,2'-(1,3,4-oxadiazole-2,5-diyl)bis[1-aminoanthraquinone]
5-хлор-3-метилбензо[b]тиофен
ГИДРАЗИД 3-ХЛОР-БЕНЗО[B]ТИОФЕН-2-КАРБОНОВОЙ КИСЛОТЫ
2-Хлор-1 ,3-динитробензол
3-Гидрокси-4'-метокси-2-нафтанилид
3-хлорбензо [б] тиофен-2-карбоксамид
2-Hydroxy-N-(4-methoxyphenyl)-11H-benzo[a]carbazole-3-carboxamide
2-амино-5,6-диметилбензотиазол
2-Chloroanthraquinone
dimethyl 4-chloropyridine-2,6-dicarboxylate
1-Бензил-2-метил-1H-имидазола
5-CHLOROBENZOTHIOPHENE
3-хлорбензо[b]тиофен-2-карбонил хлорид
3-Hydroxy-N-naphthalen-1-ylnaphthalene-2-carboxamide
5-DIMETHYLAMINO-THIOPHENE-2-CARBALDEHYDE
3 - (4-хлорбензоил) пропионовой кислоты
6-Бром-3 ,4-дигидро-2 (1Н)-хинолинон
п, п'-ДДТ
Метиловый эфир 3-хлорбензо [б] тиофен-2-карбоновой кислоты
3-хлорбензо [б] тиофен-2-карбоновой кислоты
3-гидрокси-2-нафтоил-орто-phenetidide
3-Hydroxy-N-(3-nitrophenyl)-2-naphthalenecarboxamide
АТРАЗИН
Флуоксастробин
Фенилтрихлорсилан
5-бром-2-тиофенкарбоксальдегид
4-хлорбензолсульфонилхлорид
Баклофен
pigment yellow 155
Тиофен-2 ,5-дикарбоновой кислоты
Naphthol AS-D
4,4'-дихлордифенил сульфон
2-хлорацетофенон
3,4'-Dichlorodiphenyl ether