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vapor pressure
800 hPa ( 20 °C)
Quality Level
Assay
≥95% (GC)
form
liquid
color
APHA: ≤30
bp
28 °C/1013 hPa
mp
-160 °C
transition temp
flash point -57 °C
solubility
0.048 g/L
density
0.62 g/cm3 at 20 °C
shipped in
ambient
storage temp.
room temp
InChI
1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3
InChI key
QWTDNUCVQCZILF-UHFFFAOYSA-N
Related Categories
Application
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.
Analysis Note
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - STOT SE 3
Target Organs
Central nervous system
Supplementary Hazards
WGK
WGK 2
Flash Point(F)
-59.8 °F
Flash Point(C)
-51 °C
Regulatory Information
新产品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
Power-efficient synthesis of isoprene via two-stage dehydrogenation of isopentane
World Applied Sciences Journal , 24(3) (2013)
Synthesis, characterization and photophysical properties of a new class of pyrene substituted 1, 3, 4-oxadiazole derivatives
Optical Materials, 88 (2019)
Site-selective C-H benzylation of alkanes with N-triftosylhydrazones leading to alkyl aromatics
Chem, 6(8) (2020)
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