1,3-Butadiene
SmallMolecule
T3DB_ID
T3D0156
描述
1,3-Butadiene is a simple conjugated diene with the formula C4H6. It is an important industrial chemical used as a monomer in the production of synthetic rubber. When the word butadiene is used, most of the time it refers to 1,3-butadiene. 1,3-Butadiene is inconvenient for laboratory use because it is a flammable gas subject to polymerization on storage. 3-Butadiene cyclic sulfone (sulfolene) is a convenient solid storable source for 1,3-butadiene for many laboratory purposes when the generation of sulfur dioxide byproduct in the reaction mixture is not objectionable. Long-term exposure has been associated with cardiovascular disease, there is a consistent association with leukemia, and weaker association with other cancers. Most butadiene is polymerized to produce synthetic rubber. While polybutadiene itself is a very soft, almost liquid material, copolymers prepared from mixtures of butadiene with styrene and/or acrylonitrile, such as acrylonitrile butadiene styrene (ABS), acrylonitrile butadiene (NBR) and styrene-butadiene (SBR) are tough and elastic. SBR is the material most commonly used for the production of automobile tires. Smaller amounts of butadiene are used to make the nylon intermediate, adiponitrile, by the addition of a molecule of hydrogen cyanide to each of the double bonds in a process called hydrocyanation developed by DuPont. Other synthetic rubber materials such as chloroprene, and the solvent sulfolane are also manufactured from butadiene. Butadiene is used in the industrial production of 4-vinylcyclohexene via a Diels Alder dimerization reaction and the vinylcyclohexene is a common impurity found in butadiene upon storage. Cyclooctadiene and cyclododecatriene are produced via nickel- or titanium-catalyzed dimerization and trimerization reactions, respectively. Butadiene is also useful in the synthesis of cycloalkanes and cycloalkenes, as it reacts with double and triple carbon-carbon bonds through the Diels-Alder reaction. The name butadiene can also refer to the isomer, 1,2-butadiene, which is a cumulated diene. However, this allene is difficult to prepare and has no industrial significance. This diene is also not expected to act as a diene in a Diels-Alder reaction due to its structure. To effect a Diels-Alder reaction only a conjugated diene will suffice.
类别
"Cigarette Toxin", "Household Toxin", "Industrial/Workplace Toxin", "Pollutant", "Airborne Pollutant", "Synthetic Toxin"
同义词
"1,3-Butadien", "alpha,gamma-Butadiene", "alpha,«gamma»-Butadiene", "Biethylene", "Bivinyl", "Buta-1,3-dieen", "Buta-1,3-dien", "Buta-1,3-diene", "Butadieen", "Butadien", "Butadiene", "CH22CH1CH2CH2", "CH2=CHCH=CH2", "Divinyl", "Erythrene", "Pyrrolylene", "Vinylethylene"
CAS登记号
106-99-0
化学式
C4H6
平均分子量
54.0904
单同位素质量
54.046950192
IUPAC 名称
buta-1,3-diene
传统名称
1,3-butadiene
简化分子线性输入规范
C=CC=C
InChI 标识符
InChI=1S/C4H6/c1-3-4-2/h3-4H,1-2H2
InChIKey=KAKZBPTYRLMSJV-UHFFFAOYSA-N
化合物类型
Organic compounds
大分类
Hydrocarbons
类型
Unsaturated hydrocarbons
子类
Olefins
直接大类
Alkadienes
另外分类
"Unsaturated aliphatic hydrocarbons"
取代基
"Aliphatic acyclic compound", "Alkadiene", "Unsaturated aliphatic hydrocarbon"
分子框架
Aliphatic acyclic compounds
外部描述符
"a small molecule", "butadiene"
地位
Detected and Not Quantified
起源
Exogenous
蜂窝位置
"Cytoplasm", "Extracellular"
生物流体位置
组织位置
途径
状态
Liquid
外貌
Colorless gas.
熔点/沸点/溶解度
-108.9°C//0.735 mg/mL at 25°C
日志P
1.99
暴露途径
Inhalation (L990)
毒性机制
Certain metabolites of 1,3-butadiene have been shown to bind to DNA and nucleoproteins, forming protein-DNA and DNA-DNA crosslinks. Specifically, 1,2-epoxybutene-3 and diepoxybutane react with guanine to cause crosslinking. (L990, A293)
代谢
1,3-Butadiene is absorbed following inhalation and is distributed to the adipose tissue, brain, liver, septum, and kidney. 1,3-Butadiene is believed to be metabolized in the liver by cytochrome P-450 enzymes, forming 1,2-epoxybutene-3 as the main metabolite. 1,2-Epoxybutene-3 is further transformed into 3-butene-1,2-diol by microsomal epoxide hydrolase. The metabolites of 1,3-butadiene are exhaled as carbon dioxide or excreted in the urine. (L990)
毒性值
LD50: 3.21 g/kg (Oral, Mouse) (A598) LC50: 270 000 mg/m3 over 2 hours (Inhalation, Mouse) (A598)
致死剂量
致癌性
1, carcinogenic to humans. (L135)
用途/来源
1,3-Butadiene is made from the processing of petroleum. It is used mainly to make synthetic rubber for tires. It is also used to make plastics such as acrylics, and small amounts can be found in gasoline. (L990)
最低风险等级
健康影响
Breathing high levels of 1,3-butadiene causes central nervous system damage. Chronic exposure may also cause lung damage and kidney, liver, and cardiovascular disease. In addition, 1,3-butadiene is a known human carcinogen. (L990)
症状
Breathing 1,3-butadiene may cause irritation of the eyes, nose, and throat. High levels of 1,3-butadiene can also cause, blurred vision, nausea, fatigue, headache, decreased blood pressure and pulse rate, and unconsciousness. Skin contact with liquid 1,3-butadiene can cause irritation and frostbite. (L990)
治疗
药库 ID
HMDB_ID
HMDB41792
PubChem 化合物 ID
7845
维基百科链接
http://en.wikipedia.org/wiki/1,3-butadiene
创建于
2009-03-06 18:58:11 UTC
更新于
2014-12-24 20:21:14 UTC
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