КРОТОНОВЫЙ АЛЬДЕГИД
- английское имяCROTONALDEHYDE
- CAS №4170-30-3
- CBNumberCB6733702
- ФормулаC4H6O
- мольный вес70.09
- EINECS224-030-0
- номер MDLMFCD00007003
- файл Mol4170-30-3.mol
химическое свойство
| Температура плавления | −76 °C(lit.) |
| Температура кипения | 104 °C(lit.) |
| плотность | 0.853 g/mL at 20 °C(lit.) |
| плотность пара | 2.41 (vs air) |
| давление пара | 32 mm Hg ( 20 °C) |
| показатель преломления | n |
| Fp | 48 °F |
| температура хранения | 2-8°C |
| растворимость | Miscible with alcohol, benzene, gasoline, kerosene, solvent naphtha, and toluene (Hawley, 1981) |
| форма | Colorless liquid |
| цвет | Colourless |
| Порог?обнаружения?запаха? | 0.023ppm |
| Растворимость в воде | Soluble in water. (150g/L) at 20°C. |
| Чувствительный | Air Sensitive |
| Мерк | 13,2624 |
| БРН | 1209254 |
| констант закона Генри | 1.92 x 10-5 atm?m3/mol (Buttery et al., 1971) |
| Пределы воздействия | NIOSH REL: TWA 2 ppm (6 mg/m3), IDLH 50 ppm; OSHA PEL: TWA 2 ppm; ACGIH TLV: ceiling 0.3 ppm (adopted). |
| Стабильность | Air sensitive. Highly flammable. Readily forms explosive mixtures with air. May polymerize in the presence of acids, alkalies or amines. Uncontrolled polymerisation may lead to a rapid temperature rise. Incompatible with acids, bases, amines, strong oxidizing agents, butadiene, ketones, oxygen. May contain a stabilizer. |
| LogP | 0.6 at 25℃ |
| Справочник по базе данных CAS | 4170-30-3(CAS DataBase Reference) |
| FDA UNII | 9G72074TUW |
| МАИР | 3 (Vol. 63) 1995 |
| Система регистрации веществ EPA | Crotonaldehyde (4170-30-3) |
больше
| Коды опасности | F,T+,N | |||||||||
| Заявления о рисках | 11-24/25-26-37/38-41-48/22-50-68 | |||||||||
| Заявления о безопасности | 26-28-36/37/39-45-61-16 | |||||||||
| РИДАДР | UN 1143 6.1/PG 1 | |||||||||
| OEB | B | |||||||||
| OEL | TWA: 2 ppm (6 mg/m3) (Aldehydes) | |||||||||
| WGK Германия | 3 | |||||||||
| RTECS | GP9625000 | |||||||||
| F | 9-13-23 | |||||||||
| TSCA | Yes | |||||||||
| Класс опасности | 6.1(a) | |||||||||
| Группа упаковки | I | |||||||||
| Банк данных об опасных веществах | 4170-30-3(Hazardous Substances Data) | |||||||||
| Токсичность | LD50 orally in rats: 0.3 g/kg (Smyth, Carpenter) | |||||||||
| ИДЛА | 50 ppm | |||||||||
| NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
опасность
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вредная бумага
H315：При попадании на кожу вызывает раздражение.
H335：Может вызывать раздражение верхних дыхательных путей.
H318：При попадании в глаза вызывает необратимые последствия.
H341：Предполагается, что данное вещество вызывает генетические дефекты.
H400：Чрезвычайно токсично для водных организмов.
H330：Смертельно при вдыхании.
H225：Легковоспламеняющаяся жидкость. Пары образуют с воздухом взрывоопасные смеси.
H373：Может поражать органы (Нервная система) в результате многократного или продолжительного воздействия при вдыхании.
H301+H311：Токсично при проглатывании или при контакте с кожей.
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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.
P280：Использовать перчатки/ средства защиты глаз/ лица.
P301+P310+P330：ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.
P304+P340+P310：ПРИ ВДЫХАНИИ: Свежий воздух, покой. Немедленно обратиться за медицинской помощью.
P305+P351+P338+P310：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. Немедленно обратиться за медицинской помощью.
КРОТОНОВЫЙ АЛЬДЕГИД химические свойства, назначение, производство
Химические свойства
Crotonaldehyde is water-white (turns paleyellow on contact with air) with an irritating, pungent, suffocating odor.Физические свойства
Clear, colorless to straw-colored liquid with a pungent, irritating, suffocating odor. An odor threshold concentration of 23 ppbv was reported by Nagata and Takeuchi (1990). Katz and Talbert (1930) reported experimental detection odor threshold concentrations ranged from 180 to 570 μg/m3 (63 to 200 ppbv).Использование
Crotonaldehyde is used in organic synthesis, in the manufacture of butyl alcohol and butyraldehyde, and as a warning agent in fuel gases. It is also used in the manufacture of nbutanol and sorbic acid as well as in the production of flavoring agents, surface-active agents, textiles, and insecticidal compounds.Определение
Commercial crotonaldehyde is the trans isomer.Общее описание
A clear colorless to straw colored liquid with a penetrating pungent odor. Flash point 55°F. Density 7.1 lb / gal. Very toxic by inhalation. May polymerize with the release of heat under exposure to heat or contamination. If polymerization takes place inside a container, the container may rupture violently. Less dense than water. Vapors heavier than air.Реакции воздуха и воды
Highly flammable. Slightly soluble in water.Профиль реактивности
CROTONALDEHYDE can react violently with strong oxidizing reagents, e.g., reaction with conc. nitric acid leads to instantaneous ignition [Andrussow, L., Chim. Ind. (Paris), 1961, 86, p. 542]. In contact with strong acids or bases CROTONALDEHYDE will undergo an exothermic condensation reaction. Reaction with 1,3-butadiene is particularly violent [Greenlee, K. W., Chem. Eng. News, 1948, 26, p. 1985]. Crotonaldehyde may rapidly polymerize with ethyl acetoacetate (Soriano, D.S. et al. 1988. Journal of Chemical Education 65:637.).Опасность
An animal carcinogen. Irritating to eyes, skin, and upper respiratory tract irritant. Flammable, dangerous fire risk. Explosive limits in air 2.9–15.5% by volume. Questionable carcinogen.Угроза здоровью
CROTONALDEHYDE is an extreme eye, respiratory, and skin irritant and can cause corneal damage. A 15 minute exposure at 4.1 ppm is highly irritating to the nose and upper respiratory tract and causes tearing. Brief exposure at 45 ppm proved very disagreeable with prominent eye irritation.Пожароопасность
Flammable/combustible material; may be ignited by heat, sparks or flames. Vapor 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. Readily converted by oxygen to hazardous peroxides and acids and is incompatible with caustics, ammonia, organic amines, mineral acids, and strong oxidizers. Readily resinifies to dimer when pure and slowly oxidizes to crotonic acid. Altered by light and air. Hazardous polymerization may occur. Polymerization may take place at high temperatures.Профиль безопасности
Suspected carcinogen with experimental carcinogenic data. Poison by ingestion and inhalation. Mutation data reported. An eye, skin, and mucous membrane irritant. A lachrymating material that can cause corneal burns and is very dangerous to the eyes. Caution: Keep away from heat and open flame. Keep container closed. Use with adequate ventilation. Extremely irritating to eyes, slim, mucous membranes. When necessary, the lachrymatory effect of the vapors may be counteracted by ammonia fumes. Dangerous fire hazard when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. Reacts violently with 1,3 butadlene. Violent hypergolic reaction with concentrated nitric acid. When heated to decomposition it emits acrid smoke and fumes. See also ALDEHYDES.Возможный контакт
Crotonaldehyde is used as a warning agent in fuel gases and gas line leaks; as solvent; in Crotonaldehyde 935 chemical warfare; as an intermediate in the manufacture of n-butanol and crotonic and sorbic acids; in resin and rubber antioxidant manufacture; also used as a solvent in mineral oil purification; as an alcohol denaturant.Канцерогенность
Similar to acrolein, crotonaldehyde is suspected of having tumorigenic activity and of involvement in the metabolism of N-nitrosopyrrolidine . Nevertheless, it has been proven that crotonaldehyde does have a carcinogenic effect on rats. Indeed, crotonaldehyde and nitrosopyrrolidine (a metabolite of crotonaldehyde) induced neoplastic lesions in the liver, hepatocellular carcinomas, neoplastic nodules, and liver damage when administered orally to rats over long periods of time.Экологическая судьба
Biological. Heukelekian and Rand (1955) reported a 10-d BOD value of 1.30 g/g which is 56.8% of the ThOD value of 2.29 g/g.Chemical/Physical. Slowly oxidizes in air forming crotonic acid (Windholz et al., 1983). At elevated temperatures, crotonaldehyde may polymerize (NIOSH, 1997).
Crotonaldehyde undergoes addition of water across the CH=CH bond yielding 3- hydroxybutanal (Kollig, 1995).
At an influent concentration of 1,000 mg/L, treatment with GAC resulted in effluent concentration of 544 mg/L. The adsorbability of the carbon used was 92 mg/g carbon (Guisti et al., 1974).
Перевозки
UN1143 Crotonaldehyde or Crotonaldehyde, stabilized, Hazard class: 6.1; Labels: 6.1-Poison Inhalation Hazard, 3-Flammable liquid, Inhalation Hazard Zone B.Несовместимости
Vapors may form explosive mixture with air. A strong reducing agent. Readily converted by oxygen to peroxides and acids; heat or contact with alkalis and many other substances may cause polymerization. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, nonoxidizing mineral acids; ammonia, organic amines; aliphatic amines; aromatic amines; 1,3-butadiene, strong bases. Liquid attacks some plastics, rubber, and coatingsУтилизация отходов
Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed. May be absorbed on vermiculite and burned in open incinerator or dissolved in solvent and sprayed into incineratorКРОТОНОВЫЙ АЛЬДЕГИД запасные части и сырье
сырьё
запасной предмет