1,3-ブタジエン
1,3-ブタジエン · ブタジエン · エリトレン · trans-1,3-ブタジエン · ジビニル · ビニルエチレン · 1,3-ブタンジエン · エリスレン

識別子と物理属性
| CAS No. | 106-99-0 |
|---|---|
| 分子式 | C4H6 |
| 平均分子量 | 54.09 g/mol |
| 単同位体質量 | 54.04695019 g/mol |
| SMILES | C=CC=C |
| InChIKey | KAKZBPTYRLMSJV-UHFFFAOYSA-N |
| PubChem CID | 7845 |
| ChEMBL | CHEMBL537970 |
| ChEBI | CHEBI:39478 |
| EC No. | 203-450-8 |
| DTXSID | DTXSID3020203 |
| 現地名 | 1,3-ブタジエン |
化学・物理的性質
| XLogP | 2 |
|---|---|
| 極性表面積 | 0 |
| 水素結合供与体数 | 0 |
| 水素結合受容体数 | 0 |
| 回転可能結合数 | 1 |
| 重原子数 | 4 |
| 形式電荷 | 0 |
| 複雑度 | 21 |
| LogP(分配係数) | log Kow = 1.99 |
| 臭い | MIldly aromatic odorMild aromatic or gasoline-like odor特徴臭 |
| 密度 | 0.621 at 68 °F (USCG, 1999) - Less dense than waterwill float0.6149 g/cu cm at 25 °CAbsolute density, gas at 101.325 kPa at 0 °C: 2.428 kg/cu mRelative density, gas at 101.325 kPa at 0 °C (air = 1): 1.878Density, liquid at saturation pressure at 20 °C: 0.621 kg/lCritical density: 0.245 kg/cu mRelative density (water = 1): 0.60.6149 @25 °C0.62 g/mL at 20 °C(lit.) |
| Viscosity | Gas at 101.325 kPa at 20 °C: 0.00754 cPLiquid at -40 °C: 0.33 cP |
| Color/Form | Colorless gas ... [Note: A liquid below 24 degrees F. Shipped as a liquefied compressed gas] |
| 溶解度 | Insoluble (NTP, 1992)In water, 735 mg/L at 20 °CSlightly soluble in methanol, ethanolsoluble in organic solvents such as carbon tetrachloridealcohol dissolves about 40 vols at room temp.Soluble in ethanol, ether, benzenevery soluble in acetone0.735 mg/mL at 25 °CSolubility in water, g/100ml: 0.1 (none)水:可溶0.5g/L at 20℃735mg/L(25℃) |
| Corrosivity | Non-corrosive |
| 引火点 | -105 °F (NTP, 1992)Gas-76 °C c.c.-105 °F (liquid)NA (Gas) -105 °F (Liquid)−105 °F |
| 沸点 | 24.1 °F at 760 mmHg (NTP, 1992)-4.5 °C-4 °C24 °F-4.41 °C @760 [mm Hg]−4.5 °C(lit.) |
| Decomposition | May decompose explosively when heated above 200 °C/ 1 kbar. ... When heated to decomposition it emits acrid smoke and fumes. |
| 融点 | -164 °F (NTP, 1992)-108.966 °C-108.9 °C-109 °C-108.91 °C−109 °C(lit.) |
| 蒸気密度 | 1.87 (NTP, 1992) - Heavier than airwill sink (Relative to Air)1.87 (Air = 1)Relative vapor density (air = 1): 1.91.881.9 (15 °C, vs air) |
| 蒸気圧 | 1863 mm Hg ( 21 °C) |
| 屈折率 | 1.4292 |
| 貯蔵条件 | 0-6°C |
| 外観・状態 | 無色のガス |
| 色 | Colorless to Almost colorless |
| 臭気閾値 | 0.23ppm |
| 爆発限界 | 12% |
| 凝固点 | -108.91℃ |
| 比熱容量 | Cp(liquid): 2.29 J/(g·K), at 25℃ |
| Merck | 14,1509 |
| BRN | 605258 |
| ヘンリー定数 | (x 10-2 atmm3/mol): 6.3 at 25 °C (Hine and Mookerjee, 1975) |
| 安定性 | 安定。非常に可燃性。空気と爆発性混合物を形成する可能性があります。強力な酸化剤、銅、銅合金とは相容れない。安定剤が含まれている場合があります。 |
| InChI | 1S/C4H6/c1-3-4-2/h3-4H,1-2H2 |
| InChIKey | KAKZBPTYRLMSJV-UHFFFAOYSA-N |
| SMILES | C=CC=C |
| LogP(分配係数) | 1.99 at 20℃ |
| CAS データベース | 106-99-0(CAS DataBase Reference) |
| EPAの化学物質情報 | 1,3-Butadiene (106-99-0) |
化学的特性
Butadiene is a gas, b.p. -4°C.
化学性质
ほとんど生成しないが,熱分解プロセスでは比較的多量に生成する。
安全性と法規制
| GHS 分類 | DangerH220: Extremely flammable gas [Danger Flammable gases]H340: May cause genetic defects [Danger Germ cell mutagenicity]H350: May cause cancer [Danger Carcinogenicity]P203, P210, P222, P280, P318, P377, P381, P403, P405, and P501 (click each P-code to see the statement)This chemical does not meet GHS hazard criteria for 0.1% (2 of 1783) of reports. |
|---|---|
| 規制情報 | Chemical: 1,3-ButadieneHazard Traits - CarcinogenicityDevelopmental ToxicityGenotoxicityNeurotoxicityReproductive ToxicityRespiratory ToxicityAuthoritative List - ATSDR NeurotoxicantsCA TACsEC Annex VI CMRs - Cat. 1AEC Annex VI CMRs - Cat. 1BIARC Carcinogens - 1IRIS Carcinogens - Carcin.NTP RoC - knownOEHHA RELsProp 65Report - regardless of intended function of ingredient in the product1,3-Butadiene is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,3-Butadiene are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 26-04-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/155701,3-Butadiene: HSNO Approval: HSR000988 Approved with controlsThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| その他の安全情報 | IMAP assessments - 1,3-Butadiene: Human health tier II assessment |
| 輸送ラベル(DOT) | Flammable Gas |
| 火災危険 | Behavior in Fire: Vapors heavier than air and may travel a considerable distance to a source of ignition and flashback. Containers may explode in a fire due to polymerization. (USCG, 1999)Extremely flammable. Gas/air mixtures are explosive. |
| 火災の可能性 |
用途
解説
弱い芳香性を有する引火性の液化しやすい無色の気体.融点-108.92 ℃,沸点-4.41 ℃.爆発範囲2.0~11.5体積%.エタノール,エーテルに可溶,水に不溶.共役した二重結合をもつために化学反応性は高く,とくに重合活性が高いため,貯蔵には重合防止剤および酸化防止剤の添加が必要である.石油化学の重要な原料の一つである.おもにスチレン-ブタジエンゴム(SBR),アクリロニトリル-ブタジエンゴム(NBR),ブタジエンゴムなどの合成ゴム,ABS樹脂(アクリロニトリル-ブタジエン-スチレン共重合樹脂)などの樹脂の原料となる.ほかにクロロプレン,アジポニトリル,1,4-ブタンジオールなどの合成原料としても用いられる.スチレンブタジエンゴム(SBR),ブタジエンゴム(BR)合成ゴムラテックス合成原料、スチレンブタジエンアクリロニトリル(ABS)樹脂、スチレンブタジエンメタクリレート(MBS)樹脂合成原料、化成品原料、合成ゴム(SBR,NBRなど)の原料森北出版「化学辞典(第2版)
用途
ポリブタジエン(BR),スチレン-ブタジエンゴム(SBR),ニトリルゴム(NBR),ポリクロロプレンといった合成ゴムや,アクリロニトリル-ブタジエン-スチレン樹脂(ABS樹脂)などの合成樹脂の原料
説明
1,3-Butadiene is a simple conjugated diene. It is a colourless gas with a mild aromatic or gasoline-like odour and incompatible with phenol, chlorine dioxide, copper, and crotonaldehyde. The gas is heavier than air and may travel along the ground; distant ignition is possible. It is an important industrial chemical used as a monomer in the production of synthetic rubber. Most butadiene is polymerised to produce synthetic rubber. While polybutadiene itself is a very soft, almost liquid, material, polymers prepared from mixtures of butadiene with styrene or acrylonitrile, such as ABS, are both tough and elastic. Styrene–butadiene rubber is the material most commonly used for the production of automobile tyres. Smaller amounts of butadiene are used to make nylon via the intermediate adiponitrile, other synthetic rubber materials such as chloroprene, and the solvent sulpholane. Butadiene is used in the industrial production of cyclododecatriene via a trimerisation reaction. 1,3-Butadiene structure
使用
Synthetic elastomers (styrene-butadiene, polybutadiene, neoprene, nitriles), ABS resins, chemical intermediate. 1,3-Butadiene can undergo a four-component coupling reaction with aryl Grignard reagents, and alkyl fluorides in the presence of nickel catalyst to form 1,6-octadiene carbon compound substituted with alkyl and aryl groups at the 3- and 8-positions. 1,3-Butadiene is a useful diene for Diels Alder reaction. It may be used in the synthesis of the following: 1-Silyl-substituted 1,3-butadienes, by [RuHCl(CO)(PCy3)2]-catalyzed silylative coupling of terminal (E)-1,3-dienes with vinylsilanes. Synthetic rubber and thermoplastic resins. Disilylated dimers by reacting with chlorosilanes. Octa-2,7-dien-1-ol via palladium catalyzed-hydrodimerization.
一般的な説明
1,3-Butadiene is a colorless gas with a mild, aromatic, gasoline-like odor. It is shipped as a liquefied gas under its vapor pressure. Contact with the liquid can cause frostbite. It is easily ignited. Its vapors are heavier than air and a flame can flash back to the source of leak very easily. It can asphyxiate by the displacement of air. It must be shipped inhibited as butadiene is liable to polymerization. If polymerization occurs in the container, It may violently rupture. Under prolonged exposure to fire or intense heat the containers may rupture violently and rocket. It is used to make synthetic rubber and plastics, and to make other chemicals.
製法・合成法
製造方法
Butadiene is obtained when n-butenes are dehydrogenated:n-Butenes are mostly obtained from the catalytic cracking operations carried out on various petroleum fractions; thermal cracking processes usually give low yields of butenes. The dehydrogenation of n-butenes is carried out by mixing the feed with steam (which lowers the partial pressures of the reactants) and passing over a catalyst such as mixed calcium/nickel phosphate stabilized with chromium oxide at about 650C.
調製方法
Except for a small amount of butadiene produced by the oxydehydrogenation of n-butane, most of butadiene is produced commercially as a by-product of ethylene production during the steam cracking of hydrocarbon streams. It is separated and purificated from other components by extractive distillation, using acetonitrile and dimethylformamide as solvents.
合成方法
ナフサ分解のC4留分から得られる。抽出溶剤を用いた抽出蒸留法により分離される。エチレンをナフサ分解以外から得ている地域では,ブテンの脱水素,n-ブタンの2段脱水素を行う。また,エタノール脱水素により得られるアセトアルデヒドとエタノールの脱水反応によるブタジエン製造も行われている。