Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

M32631

Sigma-Aldrich

2-Methylbutane

ReagentPlus®, ≥99%

Synonym(s):

Isopentane

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3CH2CH(CH3)2
CAS Number:
78-78-4
Molecular Weight:
72.15
Beilstein:
1730723
EC Number:
201-142-8
MDL number:
MFCD00009338
UNSPSC Code:
12191502
PubChem Substance ID:
329817967
NACRES:
NA.21

vapor density

2.6 (vs air)

Quality Level

100

vapor pressure

11.17 psi ( 20 °C)

product line

ReagentPlus®

Assay

≥99%

form

liquid

autoignition temp.

788 °F

expl. lim.

8.3 %

refractive index

n20/D 1.354 (lit.)

bp

30 °C (lit.)

mp

-160 °C

density

0.62 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCC(C)C

InChI

1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3

InChI key

QWTDNUCVQCZILF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2-Methylbutane is a flammable and highly volatile aliphatic hydrocarbon used as a solvent in organic synthesis. It is also used to flash-freeze biological samples in conjunction with dry ice or liquid nitrogen.

Application

2-Methylbutane can be used as:      
  • A reactant to synthesize isoprene by a two-stage dehydrogenation process using chromia-alumina catalyst.     
  • 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.

Other Notes

The article number M32631-4X1L will be discontinued. Please order the single bottle M32631-1L which is physically identical with the same exact specifications.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

H224,H304,H336,H411

Hazard Classifications

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

Target Organs

Central nervous system

Supplementary Hazards

EUH066

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Janak Gaire et al.
Journal of neural engineering, 15(6), 066027-066027 (2018-09-28)
Neuroinflammation has long been associated with the performance decline of intracortical microelectrodes (IMEs). Consequently, several strategies, including the use of anti-inflammatories, have been employed to mitigate the inflammation surrounding IMEs. However, these strategies have had limited success towards achieving a
Sveinung Lillehaug et al.
Scientific data, 6, 190028-190028 (2019-02-27)
The spatial pattern of transgene expression in tetracycline-controlled mouse models is governed primarily by the driver line used to introduce the tetracycline-controlled transactivator (tTA). Detailed maps showing where each tTA driver activates expression are therefore essential for designing and using
P Krustrup et al.
British journal of sports medicine, 43(11), 825-831 (2008-12-23)
To examine the effects of regular participation in recreational soccer on health profile, 36 healthy untrained Danish men aged 20-43 years were randomised into a soccer group (SO; n = 13), a running group (RU; n = 12) and a
Benedikt Galliker et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(25), 6161-6168 (2009-05-14)
We have identified two intermediates in the autoxidation of NO*: ONOO*, which was detected by EPR spectroscopy at 295 K and atmospheric pressure in the gas phase, and ONOONO, a red substance produced at 113 K in 2-methylbutane. The red
Nahid A Khan et al.
EMBO molecular medicine, 6(6), 721-731 (2014-04-09)
Nutrient availability is the major regulator of life and reproduction, and a complex cellular signaling network has evolved to adapt organisms to fasting. These sensor pathways monitor cellular energy metabolism, especially mitochondrial ATP production and NAD(+)/NADH ratio, as major signals
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service