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320196

Sigma-Aldrich

tert-Butyl methyl ether

reagent grade, 98%

Synonym(s):

MTBE, Methyl tert-butyl ether

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About This Item

Linear Formula:
(CH3)3COCH3
CAS Number:
1634-04-4
Molecular Weight:
88.15
Beilstein/REAXYS Number:
1730942
EC Number:
216-653-1
MDL number:
MFCD00008812
UNSPSC Code:
12352112
PubChem Substance ID:
329753965
NACRES:
NA.07

grade

reagent grade

Quality Level

100

vapor density

3.1 (vs air)

vapor pressure

4.05 psi ( 20 °C)

assay

98%

form

liquid

autoignition temp.

705 °F

expl. lim.

15.1 %

refractive index

n20/D 1.369 (lit.)

bp

55-56 °C (lit.)

mp

-110 °C

density

0.74 g/mL at 25 °C (lit.)

SMILES string

COC(C)(C)C

InChI

1S/C5H12O/c1-5(2,3)6-4/h1-4H3

InChI key

BZLVMXJERCGZMT-UHFFFAOYSA-N

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Related Categories

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H315

Hazard Classifications

Flam. Liq. 2 - Skin Irrit. 2

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

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Removal of methyl tert-butyl ether (MTBE) with Nafion.
Lien HL and Zhang WX
Journal of Hazardous Materials, 144(1), 194-199 (2007)
J R Hanson et al.
Applied and environmental microbiology, 65(11), 4788-4792 (1999-11-05)
A bacterial strain, PM1, which is able to utilize methyl tert-butyl ether (MTBE) as its sole carbon and energy source, was isolated from a mixed microbial consortium in a compost biofilter capable of degrading MTBE. Initial linear rates of MTBE
Kun-Chang Huang et al.
Chemosphere, 49(4), 413-420 (2002-10-09)
The kinetics of heat-assisted persulfate oxidation of methyl tert-butyl ether (MTBE) in aqueous solutions at various pH, temperature, oxidant concentration and ionic strength levels was studied. The MTBE degradation was found to follow a pseudo-first-order decay model. The pseudo-first-order rate
R J Steffan et al.
Applied and environmental microbiology, 63(11), 4216-4222 (1997-11-15)
Several propane-oxidizing bacteria were tested for their ability to degrade gasoline oxygenates, including methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME). Both a laboratory strain and natural isolates were able to degrade each compound after
Sarah K Abbott et al.
Lipids, 48(3), 307-318 (2013-01-29)
We have developed a protocol suitable for high-throughput lipidomic analysis of human brain samples. The traditional Folch extraction (using chloroform and glass-glass homogenization) was compared to a high-throughput method combining methyl-tert-butyl ether (MTBE) extraction with mechanical homogenization utilizing ceramic beads.
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