蒸汽压
9.98 psi ( 20 °C)
质量水平
检测方案
98%
形式
liquid
折射率
n20/D 1.378 (lit.)
bp
31 °C (lit.)
mp
−137 °C (lit.)
密度
0.65 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
CCC(C)=C
InChI
1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3
InChI key
MHNNAWXXUZQSNM-UHFFFAOYSA-N
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一般描述
本文研究强酸性大孔树脂催化剂上乙醇醚化反应中 2-甲基-1-丁烯的反应性 。此外，本文还研究了在硝基甲烷中 2-甲基-1-丁烯与氢和氯化氘加成的动力学和机理。
应用
- Combustion Properties Analysis: A detailed study on the combustion properties of a gasoline-like blend of pentene isomers, including 2-Methyl-1-butene, provided insights into laminar flame speed, ignition delay time, and CO laser absorption, aiding in the optimization of fuel formulations for enhanced engine performance (Gregoire et al., 2023).
- Hydrogenation Mechanism Study: Research utilizing the parahydrogen-induced polarization technique explored the mechanisms of methylenecyclobutane hydrogenation over supported metal catalysts, with 2-Methyl-1-butene serving as a key intermediate, offering potential advancements in catalytic process development (Salnikov et al., 2022).
- Reaction Kinetics with Hydrogen Atoms: An extensive theoretical study examined the reactions of hydrogen atoms with small alkenes, including 2-Methyl-1-butene, shedding light on the hierarchical reaction mechanisms crucial for understanding and designing better chemical synthesis processes (Power et al., 2021).
- Ozonolysis of Asymmetric Alkenes: A study on the ozonolysis of asymmetric alkenes, including 2-Methyl-1-butene, used matrix isolation and FT-IR spectroscopy to investigate the chemical pathways, providing valuable insights into atmospheric chemistry and pollutant degradation (Wang et al., 2020).
警示用语：
Danger
危险声明
危险分类
Flam. Liq. 1
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Faceshields, Gloves
法规信息
危险化学品
Etherification rates of 2-methyl-2-butene and 2-methyl-1-butene with ethanol for environmentally clean gasoline production.
Oktar N, et al.
Journal of Chemical Technology and Biotechnology, 74(2), 155-161 (1999)
Kinetics and mechanism of addition of acids to olefins. III. Addition of hydrogen chloride to 2-methyl-1-butene, 2-methyl-2-butene, and isoprene in nitromethane.
Pocker Y, et al.
Journal of the American Chemical Society, 91(15), 4199-4205 (1969)
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