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蒸汽压
800 hPa ( 20 °C)
质量水平
方案
≥95% (GC)
表单
liquid
颜色
APHA: ≤30
沸点
28 °C/1013 hPa
mp
-160 °C
转变温度
flash point -57 °C
溶解性
0.048 g/L
密度
0.62 g/cm3 at 20 °C
运输
ambient
储存温度
room temp
SMILES字符串
C(CC)(C)C
InChI
1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3
InChI key
QWTDNUCVQCZILF-UHFFFAOYSA-N
应用
2-Methylbutane can be used as a reactant to synthesize:
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.
- Isoprene by two-stage dehydrogenation process using chromia-alumina catalyst.
- Alkyl aromatic compounds via silver-catalyzed selective C(sp3)–H benzylation reaction in the presence of N-triftosylhydrazones as carbene precursor.
It can also be used as a weakly polar solvent to study the intramolecular charge transfer (ICT) effect and the solvatochromic behavior of the pyrene substituted 1,3,4-oxadiazole derivatives.
包装
M-Bottle for Solvents
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As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!
分析说明
Assay (GC): 95% min
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
Color (APHA): 30 max
Form: Clear liquid
Infrared Spectrum: Conforms to standard
警示用语：
Danger
危险分类
Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - STOT SE 3
靶器官
Central nervous system
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
-59.8 °F - closed cup
闪点(°C)
-51 °C - closed cup
Power-efficient synthesis of isoprene via two-stage dehydrogenation of isopentane
Karimov OK, et al.
World Applied Sciences Journal , 24(3) (2013)
Site-selective C-H benzylation of alkanes with N-triftosylhydrazones leading to alkyl aromatics
Liu Zhaohong, et al.
Chem, 6(8) (2020)
Synthesis, characterization and photophysical properties of a new class of pyrene substituted 1, 3, 4-oxadiazole derivatives
Najare Mahesh S, et al.
Optical Materials, 88 (2019)
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