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Гексан

  • английское имяHexane
  • CAS №110-54-3
  • CBNumberCB1852811
  • ФормулаC6H14
  • мольный вес86.18
  • EINECS203-777-6
  • номер MDLMFCD00009520
  • файл Mol110-54-3.mol
химическое свойство
Температура плавления -95 °C
Температура кипения 68.95 °C(lit.)
плотность 0.659 g/mL at 25 °C(lit.)
плотность пара 3.5 (vs air)
давление пара 40 mm Hg ( 20 °C)
показатель преломления n20/D 1.388
Fp 30 °F
температура хранения Store at +5°C to +30°C.
растворимость Very soluble in ethanol, ethyl ether and chloroform.
форма Liquid
пка >14 (Schwarzenbach et al., 1993)
цвет Colorless
Удельный вес 0.660 (20/4℃)
Запах Mild gasoline-like odor detectable at 65 to 248 ppm
Относительная полярность 0.009
Пределы взрываемости 1.0-8.1%(V)
Порог?обнаружения?запаха? 1.5ppm
Вязкость 0.31 mPas 20 deg C
Растворимость в воде insoluble
λмакс λ: 200 nm Amax: ≤0.70
λ: 225 nm Amax: ≤0.10
λ: 250 nm Amax: ≤0.01
Мерк 14,4694
БРН 1730733
констант закона Генри 0.238, 0.413, 0.883, 0.768, and 1.56 at 10, 15, 20, 25, and 30 °C, respectively (EPICS, Ashworth et al., 1988)
Пределы воздействия TLV-TWA 50 ppm (~175 mg/m3) (ACGIH), 500 ppm (~1750 mg/m3) (OSHA); IDLH 5000 ppm (NIOSH).
Диэлектрическая постоянная 2.0(-90℃)
Стабильность Stable. Incompatible with oxidizing agents, chlorine, fluorine, magnesium perchlorate. Highly flammable. Readily forms explosive mixtures with air. Note low flash point.
ИнЧИКей VLKZOEOYAKHREP-UHFFFAOYSA-N
LogP 4 at 20℃ and pH7
FDA 21 CFR 173.270; 175.105; 175.320; 176.200; 73.345; 73.615
Вещества, добавляемые в пищу (ранее EAFUS) HEXANE
Справочник по базе данных CAS 110-54-3(CAS DataBase Reference)
Рейтинг продуктов питания EWG 4-7
FDA UNII 2DDG612ED8
Предложение 65 Список n-Hexane
Справочник по химии NIST Hexane(110-54-3)
Система регистрации веществ EPA Hexane (110-54-3)
больше
Заявления об опасности и безопасности
Коды опасности F,Xn,N
Заявления о рисках 11-38-50/53-65-67-62-51/53-48/20-36/37/38
Заявления о безопасности 9-16-29-33-60-61-62-36/37-45-36/37/39-53-26
РИДАДР UN 3295 3/PG 2
OEB A
OEL TWA: 50 ppm (180 mg/m3)
WGK Германия 3
RTECS MN9275000
F 3-10
Температура самовоспламенения 225 °C
TSCA Yes
Класс опасности 3
Группа упаковки II
кода HS 29011000
Банк данных об опасных веществах 110-54-3(Hazardous Substances Data)
Токсичность LC50 (4 hr) in mice by inhalation: 48000 ppm; LD50 orally in rats: 32.0 g/kg (Couri, Milks)
ИДЛА 1,100 ppm [10% LEL]
NFPA 704:
3
0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms

  • сигнальный язык

    опасность

  • вредная бумага

    H315:При попадании на кожу вызывает раздражение.

    H411:Токсично для водных организмов с долгосрочными последствиями.

    H225:Легковоспламеняющаяся жидкость. Пары образуют с воздухом взрывоопасные смеси.

    H304:Может быть смертельным при проглатывании и последующем попадании в дыхательные пути.

    H336:Может вызывать сонливость или головокружение.

    H361f:Предполагается, что данное вещество может отрицательно повлиять на способность к деторождению.

    H373:Может поражать органы (Нервная система) в результате многократного или продолжительного воздействия при вдыхании.

  • оператор предупредительных мер

    P201:Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.

    P210:Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.

    P273:Избегать попадания в окружающую среду.

    P301+P310:ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.

    P303+P361+P353:ПРИ ПОПАДАНИИ НА КОЖУ (или волосы): Снять/удалить немедленно всю загрязненную одежду. Промыть кожу водой.

    P331:немедленно всю загрязненную одежду. Промыть кожу водой. Не вызывать рвоту!

Гексан химические свойства, назначение, производство

Химические свойства

n-Hexane is a highly flammable liquid, usually isolated from crude oil, and has extensive industrial applications as a solvent in adhesive bandage factories and other industries.
n-Hexane
It is highly toxic, triggering several adverse health effects, i.e., nausea, skin irritation, dizziness, numbness of limbs, CNS depression, vertigo, and respiratory tract irritation to animals and humans. Occupational exposure of industrial workers has demonstrated motor polyneuropathy. Workers associated with long-term glue sniffi ng showed adverse effects in the form of degeneration of axons and nerve terminals.

Физические свойства

Clear, colorless, very flammable liquid with a faint, gasoline-like odor. An odor threshold concentration of 1.5 ppmv was reported by Nagata and Takeuchi (1990).

Использование

n-Hexane is a chief constituent of petroleumether, gasoline, and rubber solvent. It is usedas a solvent for adhesives, vegetable oils,and in organic analysis, and for denaturingalcohol.

Определение

ChEBI: An unbranched alkane containing six carbon atoms.

Общее описание

Clear colorless liquids with a petroleum-like odor. Flash points -9°F. Less dense than water and insoluble in water. Vapors heavier than air. Used as a solvent, paint thinner, and chemical reaction medium.

Реакции воздуха и воды

Highly flammable. Insoluble in water.

Профиль реактивности

HEXANE may be sensitive to light. Hexane may also be sensitive to prolonged exposure to heat. Hexane can react vigorously with oxidizing materials. This would include compounds such as liquid chlorine, concentrated O2, sodium hypochlorite and calcium hypochlorite. Hexane is also incompatible with dinitrogen tetraoxide. Hexane will attack some forms of plastics, rubber and coatings. .

Опасность

Flammable, dangerous fire risk.

Угроза здоровью

n-Hexane is a respiratory tract irritant andat high concentrations a narcotic. Its acutetoxicity is greater than that of n-pentane.Exposure to a concentration of 40,000 ppmfor an hour caused convulsions and death inmice. In humans a 10-minute exposure toabout 5000 ppm may produce hallucination,distorted vision, headache, dizziness, nausea,and irritation of eyes and throat. Chronicexposure to n-hexane may cause polyneuritis.
The metabolites of n-hexane injected inguinea pigs were reported as 2,5- hexanedioneand 5-hydroxy-2-hexanone, which arealso metabolites of methyl butyl ketone(DiVincenzo et al. 1976). Thus methyl butylketone and n- hexane should have similartoxicities. The neurotoxic metabolite, 2,5-hexanedione, however, is produced considerablyless in n-hexane. However, in the caseof hexane, the neurotoxic metabolite 2,5-hexanedione is produced to a much lesserextent. Continuous exposure to 250 ppmn-hexane produced neurotoxic effects in animals. Occupational exposure to 500 ppmmay cause polyneuropathy (ACGIH 1986).
Inhalation of n-hexane vapors have shownreproductive effects in rats and mice.

Воспламеняемость и взрывоопасность

Hexane is extremely flammable (NFPA rating = 3), and its vapor can travel a considerable distance to an ignition source and "flash back." Hexane vapor forms explosive mixtures with air at concentrations of 1.1 to 7.5 % (by volume).
Hydrocarbons of significantly higher molecular weight have correspondingly higher vapor pressures and therefore present a reduced flammability hazard. Carbon dioxide or dry chemical extinguishers should be used for hexane fires.

Химическая реактивность

Reactivity with Water: No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Возможный контакт

n-Hexane is industrial chemical, emul sifier, in manufacture of plastics, resins; as a solvent, par ticularly in the extraction of edible fats and oils; as a laboratory reagent; and as the liquid in low temperature thermometers. Technical and commercial grades consist of 45 85% hexane, as well as cyclopentanes, isohexane, and 1% to 6% benzene.

Канцерогенность

Male rabbits exposed to 3000 ppm hexane (8 h/day, 6 days/week for 24 weeks) developed papillary proliferation of nonciliated bronchiolar cells. No tumors were found in mice painted with hexane and croton oil as cocarcinogen, presumably for the lifetime of each animal. Hexane is inactive as a tumorpromoting agent.

Экологическая судьба

Biological. Hexane may biodegrade in two ways. The first is the formation of hexyl hydroperoxide, which decomposes to 1-hexanol followed by oxidation to hexanoic acid. The other pathway involves dehydrogenation to 1-hexene, which may react with water giving 1-hexanol (Dugan, 1972). Microorganisms can oxidize alkanes under aerobic conditions (Singer and Finnerty, 1984). The most common degradative pathway involves the oxidation of the terminal methyl group forming 1-hexanol. The alcohol may undergo a series of dehydrogenation steps forming a hexanal followed by oxidation to form hexanoic acid. The fatty acid may then be metabolized by β-oxidation to form the mineralization products, carbon dioxide and water (Singer and Finnerty, 1984).
Photolytic. An aqueous solution irradiated by UV light at 50 °C for 1 d resulted in a 50.51% yield of carbon dioxide (Knoevenagel and Himmelreich, 1976). Synthetic air containing gaseous nitrous acid and exposed to artificial sunlight (λ = 300–450 nm) photooxidized hexane into two isomers of hexyl nitrate and peroxyacetal nitrate (Cox et al., 1980).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water vapor.

хранилище

hexane should be used only in areas free of ignition sources, and quantities greater than 1 liter should be stored in tightly sealed metal containers in areas separate from oxidizers.

Перевозки

UN1208 Hexanes, Hazard Class: 3; Labels: 3-Flammable liquid.

Методы очистки

Purify as for n-heptane. Modifications include the use of chlorosulfonic acid or 35% fuming H2SO4 instead of conc H2SO4 in washing the alkane, and final drying and distilling from sodium hydride. Unsaturated impurities can be removed by shaking the hexane with nitrating acid (58% H2SO4, 25% conc HNO3, 17% water, or 50% HNO3, 50% H2SO4), then washing the hydrocarbon layer with conc H2SO4, followed by H2O, drying, and distilling over sodium or n-butyl lithium. It can also be purified by distillation under nitrogen from sodium benzophenone ketyl solubilised with tetraglyme. Also purify it by passage through a silica gel column followed by distillation [Kajii et al. J Phys Chem 91 2791 1987]. It is a FLAMMABLE liquid and a possible nerve toxin. [Beilstein 1 IV 338.] Rapid purification: Distil, discarding the first forerun and stored over 4A molecular sieves.

Несовместимости

May form explosive mixture with air. Contact with strong oxidizers may cause fire and explo sions. Contact with dinitrogen tetraoxide may explode @ 28℃.Attacks some plastics, rubber and coatings. May accumulate static electrical charges, and may cause ignition of its vapors.

Утилизация отходов

Dissolve or mix the material with a combustible solvent and burn in a chemical incinera tor equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

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