Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство запасные части и сырье Обзор
ПРОПИОНИТРИЛ структурированное изображение

ПРОПИОНИТРИЛ

  • английское имяPropionitrile
  • CAS №107-12-0
  • CBNumberCB9852701
  • ФормулаC3H5N
  • мольный вес55.08
  • EINECS203-464-4
  • номер MDLMFCD00001948
  • файл Mol107-12-0.mol
химическое свойство
Температура плавления -93 °C (lit.)
Температура кипения 97 °C (lit.)
плотность 0.772 g/mL at 25 °C (lit.)
давление пара 53.33-63.195hPa at 22.05-25℃
показатель преломления n20/D 1.366(lit.)
Fp 43 °F
температура хранения Flammables area
растворимость soluble in water at 40°C is 11.9 g/100 g H20; miscible with alcohol, ether, dimethylformamide
форма Oil
цвет Clear Colourless
РН 10 (20°C, 50g/L in H2O)
Пределы взрываемости 3.1-14% (v/v)
Растворимость в воде decomposes. 5-10 g/100 mL at 23 ºC
Точка замерзания -93℃
Мерк 14,7827
БРН 773680
Пределы воздействия TLV-TWA 14 mg/m3 (6 ppm) (NIOSH).
Диэлектрическая постоянная 27.7(20℃)
Стабильность Stable. Flammable. Note low flash point. Incompatible with strong oxidising agents, strong bases, strong acids, strong reducing agents.
LogP -0.1-0.16
Dissociation constant 33.54
Справочник по базе данных CAS 107-12-0(CAS DataBase Reference)
Рейтинг продуктов питания EWG 1
FDA UNII E16N05FX3S
Справочник по химии NIST Propanenitrile(107-12-0)
Система регистрации веществ EPA Propanenitrile (107-12-0)
UNSPSC Code 12352117
NACRES NA.22
больше
Заявления об опасности и безопасности
Коды опасности F,T+,T
Заявления о рисках 11-20-25-27-36-23/24/25
Заявления о безопасности 9-16-28-36/37-45-27
РИДАДР UN 2404 3/PG 2
OEB A
OEL TWA: 6 ppm (14 mg/m3)
WGK Германия 1
RTECS UF9625000
Температура самовоспламенения 515°C
TSCA Yes
Класс опасности 3
Группа упаковки II
кода HS 29269095
Банк данных об опасных веществах 107-12-0(Hazardous Substances Data)
Токсичность LD50 orally in rats: 39 mg/kg (Smyth)
NFPA 704:
3
4 1

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictogramsGHS hazard pictograms

  • вредная бумага

    H319:При попадании в глаза вызывает выраженное раздражение.

    H310:Смертельно при попадании на кожу.

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

    H300:Смертельно при проглатывании.

    H331:Токсично при вдыхании.

  • оператор предупредительных мер

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

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

    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.

    P405:Хранить в недоступном для посторонних месте.

ПРОПИОНИТРИЛ химические свойства, назначение, производство

Химические свойства

Propionitrile is a colorless liquid with a pleasant, sweetish, ethereal odor. Propionitrile [107-12-0], ethyl cyanide, CH3CH2CN, is a colorless liquid which is miscible with water, ethanol, dimethylformamide, and diethyl ether. The physical properties are listed in Table 1. Propionitrile is obtained either by hydrogenation of acrylonitrile or by the gas-phase reaction of propanal or propanol with ammonia. It is also obtained as a byproduct in the electrohydrodimerization of acrylonitrile to adiponitrile (EHD process).

Использование

Propionitrile is an intermediate for organic syntheses, e.g. Houben-Hoesch reaction, as well as for pharmaceuticals, e.g. ketoprofen and fragrances.

Методы производства

Propionitnle may be prepared by dehydration of propionamide (or propionic acid plus ammonia) or by distilling ethyl sulfate and concentrated aqueous KCN. It also is formed as a byproduct of the electrohydrodimerization of acrylonitrile or by the hydrogenation of acrylonitrile with the use of copper, rhodium or nickle catalysts . U.S. production is estimated for 1980 to range between 10-15 million pounds.

Определение

ChEBI: A nitrile that is acrylonitrile in which the carbon-carbon double bond has been reduced to a single bond.

Общее описание

A colorless liquid with an ether-like odor. Density 0.683 g / cm3. Flash point 61°F. Toxic by inhalation, skin absorption, and ingestion. Vapors are heavier than air. Used as a solvent, and to make other chemicals.

Реакции воздуха и воды

Highly flammable. Soluble in water.

Профиль реактивности

Propionitrile is incompatible with strong acids, strong bases, strong oxidizing agents and strong reducing agents. After refluxing for 24 hours at 221°F, a mixture of Propionitrile with N-bromosuccinimide exploded.

Опасность

Toxic by ingestion and inhalation. Flammable, dangerous fire risk.

Угроза здоровью

Propionitrile is highly toxic. This super toxic compound has a probable oral lethal dose in humans of less than 5 mg/kg or a taste (less than 7 drops) for a 70 kg (150 lb.) person. It is a mild to moderate skin and eye irritant.

Пожароопасность

When heated to decomposition, Propionitrile emits toxic fumes of nitrogen oxides and cyanide. Propionitrile is a flammable/combustible material and may be ignited by heat, sparks or flames. Vapors may travel to a source of ignition and flash back. Container may explode in heat of fire. Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Generates cyanide ions. Poisonous on contact with acids. stable, but may become unstable at elevated temperatures and pressures.

Промышленное использование

Propionitnle is used as a selective solvent in the chemical industry and in petroleum refining and as a dielectric fluid . It has also been used experimentally as an ulcerogen .

Профиль безопасности

Poison by ingestion, skin contact, intravenous, and intraperitoneal routes. Moderately toxic by inhalation. Experimental teratogenic effects. Other experimental reproductive effects. A skin and eye irritant. Dangerous fire hazard when exposed to heat, flame (sparks), oxidners. Mixture with N- bromosuccinimide may explode when heated. To fight fire, use water spray, foam, mist, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx and CN-. Used as a solvent in petroleum refining, and as a raw material for drug manufacture. See also NITRILES.

Возможный контакт

Used as a solvent in petroleum refin- ing, as a chemical intermediate; a raw material for drug manufacture; and a setting agent.

Перевозки

UN2404 Propionitrile, Hazard Class: 3; Labels: 3-Flammable liquid, 6.1-Poisonous material. UN1992 Flammable liquids, toxic, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid, 6.1-Poisonous materials, Technical Name Required.

Методы очистки

Shake the nitrile with dilute HCl (20%), or with conc HCl until the odour of isonitrile has gone, then wash it with water, and aqueous K2CO3. After a preliminary drying with silica gel or Linde type 4A molecular sieves, it is stirred with CaH2 until hydrogen evolution ceases, then decant and distil from P2O5 (not more than 5g/L, to minimise gel formation). Finally, it is refluxed with, and slowly distilled from CaH2 (5g/L), taking precautions to exclude moisture. [Beilstein 2 IV 728.]

Несовместимости

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlo- rine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides., reducing agents. Hydrogen cyanide is produced when propionitrile is heated to decomposition. Reacts with acids, steam, warm water; producing toxic and flammable hydrogen cyanide fumes. Nitriles may polymerize in the presence of metals and some metal compounds. They are incompati- ble with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents. Acetonitrile and propionitrile are soluble in water, but nitriles higher than propionitrile have low aqueous solubility. They are also insoluble in aqueous acids .

Утилизация отходов

Alcoholic NaOH followed by calcium hypochlorite may be used, as may incineration . Consult with environmental regulatory agencies for guid- ance 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.