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MX0760

Supelco

2-Methylbutane

Practical

Synonym(s):

2-Methylbutane, Isopentane

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About This Item

Linear Formula:
(CH3)2CHCH2CH3
CAS Number:
MDL number:
UNSPSC Code:
12191502
EC Index Number:
201-142-8

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

Application

2-Methylbutane can be used as a reactant to synthesize:
  • 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

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 1 - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

-59.8 °F - closed cup

Flash Point(C)

-51 °C - closed cup


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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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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