|Molar mass||54.0916 g/mol|
or refrigerated liquid
|Odor||mildly aromatic or gasoline-like|
|Density||0.6149 g/cm3 at 25 °C, solid
0.64 g/cm3 at −6 °C, liquid
|Melting point||−108.9 °C (−164.0 °F; 164.2 K)|
|Boiling point||−4.4 °C (24.1 °F; 268.8 K)|
|0.735 g/100 mL|
|Solubility||very soluble in acetone
soluble in ether, ethanol
|Vapor pressure||2.4 atm (20°C)|
Refractive index (nD)
|Viscosity||0.25 cP at 0 °C|
|Main hazards||Flammable, irritative, carcinogen|
|R-phrases||R45 R46 R12|
|Flash point||−85 °C (−121 °F; 188 K) liquid flash point|
|420 °C (788 °F; 693 K)|
LD50 (Median lethal dose)
|548 mg/kg (rat, oral)|
|US health exposure limits (NIOSH):|
|TWA 1 ppm ST 5 ppm|
|potential occupational carcinogen|
IDLH (Immediate danger)
|Supplementary data page|
|Refractive index (n),
Dielectric constant (εr), etc.
|UV, IR, NMR, MS|
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
|what is: / ?)(|
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.
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.
Although butadiene breaks down quickly in the atmosphere, it is nevertheless found in ambient air in urban and suburban areas as a consequence of its constant emission from motor vehicles. The EPA lists it as the "mobile source air toxic" with the highest normalized risk factor, exceeding that of formaldehyde, the second riskiest air toxic emitted by motor vehicles, by a factor of more than 20.
In 1863, a French chemist isolated a previously unknown hydrocarbon from the pyrolysis of amyl alcohol. This hydrocarbon was identified as butadiene in 1886, after Henry Edward Armstrong isolated it from among the pyrolysis products of petroleum. In 1910, the Russian chemist Sergei Lebedev polymerized butadiene, and obtained a material with rubber-like properties. This polymer was, however, found to be too soft to replace natural rubber in many applications, notably automobile tires.
The butadiene industry originated in the years leading up to World War II. Many of the belligerent nations realized that in the event of war, they could be cut off from rubber plantations controlled by the British Empire, and sought to reduce their dependence on natural rubber. In 1929, Eduard Tschunker and Walter Bock, working for IG Farben in Germany, made a copolymer of styrene and butadiene that could be used in automobile tires. Worldwide production quickly ensued, with butadiene being produced from grain alcohol in the Soviet Union and the United States and from coal-derived acetylene in Germany.
Extraction from C4 hydrocarbons
In the United States, western Europe, and Japan, butadiene is produced as a byproduct of the steam cracking process used to produce ethylene and other olefins. When mixed with steam and briefly heated to very high temperatures (often over 900 °C), aliphatic hydrocarbons give up hydrogen to produce a complex mixture of unsaturated hydrocarbons, including butadiene. The quantity of butadiene produced depends on the hydrocarbons used as feed. Light feeds, such as ethane, give primarily ethylene when cracked, but heavier feeds favor the formation of heavier olefins, butadiene, and aromatic hydrocarbons.
Butadiene is typically isolated from the other four-carbon hydrocarbons produced in steam cracking by extractive distillation using a polar aprotic solvent such as acetonitrile, N-methylpyrrolidone, furfural, or dimethylformamide, from which it is then stripped by distillation.
From dehydrogenation of n-butane
Butadiene can also be produced by the catalytic dehydrogenation of normal butane (n-butane). The first such post-war commercial plant, producing 65,000 tons per year of butadiene, began operations in 1957 in Houston, Texas. Prior to that, in the 1940s the U. S. War Department constructed several plants in Borger, TX, Toledo, OH, and El Segundo, CA to produce synthetic rubber for the war effort as part of the United States Synthetic Rubber Program. Total capacity was 68 KMTA (Kilo Metric Tons per Annum).
Today, butadiene from n-butane is commercially practiced using the Houdry catadiene process, which was developed during WWII.
In other parts of the world, including South America, Eastern Europe, China, and India, butadiene was also produced from ethanol. While not competitive with steam cracking for producing large volumes of butadiene, lower capital costs make production from ethanol a viable option for smaller-capacity plants. Two processes were in use.
This process was the basis for the Soviet Union's synthetic rubber industry during and after World War II, and it remained in limited use in Russia and other parts of eastern Europe until the end of the 1970s. At the same time this type of manufacture was canceled in Brazil. Nowadays there is no industrial production of butadiene from ethanol. Lately Lanxess has announced plans to produce butadiene from ethanol.
In the other, two-step process, developed by the Russian emigree chemist Ivan Ostromislensky, ethanol is oxidized to acetaldehyde, which reacts with additional ethanol over a tantalum-promoted porous silica catalyst at 325–350 °C to yield butadiene:
This process was one of the three used in the United States to produce "government rubber" during World War II, though it was not preferred because it is less economical than the butane or butene routes for the large volumes needed. Still, three plants with a total capacity of 200 KMTA[when defined as?] were constructed in the US (Institute, WV; Louisville, KY; and Kobuta, PA ) with start-ups completed in 1943, the Louisville plant initially created butadiene from acetylene generated by an associated Calcium Carbide plant. The process remains in use today in China and India.
1,3-Butadiene can also be produced by catalytic dehydrogenation of normal butenes. This method was also used by the United States Synthetic Rubber Program (USSRP) during World War II. The process was much more economical than the alcohol route but competed with aviation gasoline for available butene molecules. The USSRP constructed several plants in Baton Rouge and Lake Charles, LA; Houston, Baytown, and Port Neches, TX; and Torrance, CA. Total annual production was 275 KMTA.
In the 1960s, a Houston company known as "Petro-Tex" patented a process to produce butadiene from normal butenes by oxidative dehydrogenation using a proprietary catalyst. It is thought to be no longer practiced commercially.
After the WWII the production from butenes became the major type of production in USSR.
For laboratory use
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.
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/or 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. Vinylcyclohexene is a common impurity found in butadiene upon storage due to dimerization. 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.
Environmental health and safety
Acute exposure results in irritation of the mucous membranes, Higher levels can result in neurological effects such as blurred vision, fatigue, headache and vertigo. Exposure to the skin can lead to frostbite.
Long-term exposure has been associated with cardiovascular disease, there is a consistent association with leukemia, and weaker association with other cancers.
1,3-Butadiene is listed as a known carcinogen by the Agency for Toxic Substances Disease Registry and the US EPA. The American Conference of Governmental Industrial Hygienists (ACGIH) lists the chemical as a suspected carcinogen. The Natural Resource Defense Council (NRDC) lists some disease clusters that are suspected to be associated with this chemical. Some researchers have concluded it is the most potent carcinogen in cigarette smoke, twice as potent as the runner up acrylonitrile
1,3-Butadiene is also a suspected human teratogen. Prolonged and excessive exposure can affect many areas in the human body; blood, brain, eye, heart, kidney, lung, nose and throat have all been shown to react to the presence of excessive 1,3-Butadiene. Animal data suggest that women have a higher sensitivity to possible carcinogenic effects of butadiene over men when exposed to the chemical. This may be due to estrogen receptor impacts. While these data reveal important implications to the risks of human exposure to butadiene, more data are necessary to draw conclusive risk assessments. There is also a lack of human data for the effects of butadiene on reproductive and development shown to occur in mice, but animal studies have shown breathing butadiene during pregnancy can increase the number of birth defects, and humans have the same hormone systems as animals.
Storage of butadiene as a compressed, liquified gas carries a specific and unusual hazard. Over time, polymerization can begin, creating a crust of solidified material (popcorn polymer, named for its appearance) inside the vapor space of cylinder. If the cylinder is then disturbed, the crust can contact the liquid and initiate an auto-catalytic polymerization. The heat released accelerates the reaction, possibly leading to cylinder rupture. Inhibitors are typically added to reduce this hazard, but butadiene cylinders should still be considered short-shelf life items. The hazard presented by popcorn polymer is also present in bulk commercial storage tanks. It is important to keep the oxygen concentration in the tanks and any process wash water low in order to reduce the rate of polymerization.
As with other light hydrocarbons, butadiene leaks can be detected by the formation of ice balls (from the evaporative freezing of water out of the atmosphere) even when the temperature is well above 0 °C.
1,3-Butadiene is recognized as a Highly Reactive Volatile Organic Compound (HRVOC) for its potential to readily form ozone, and as such, emissions of the chemical are highly regulated by TCEQ in parts of the Houston-Brazoria-Galveston Ozone Non-Attainment Area.
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- Alternative Fuels and Advanced Vehicles Data Center. "Alternative & Advanced Vehicles: Pollutants and Health". Energy Efficiency and Renewable Energy, US DOE. Retrieved 2014-09-02.
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- NPI sheet
- Health Effects https://www.osha.gov/SLTC/butadiene/index.html
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- EPA website
- 1,3-Butadiene – Agency for Toxic Substances and Disease Registry
- 1,3-Butadiene – CDC - NIOSH Pocket Guide to Chemical Hazards
- National Pollutant Inventory – 1,3-Butadiene