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293210

Supelco

tert-Butyl methyl ether

HPLC grade, suitable for HPLC, 99.8%

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:
1730942
EC Number:
216-653-1
MDL number:
MFCD00008812
UNSPSC Code:
12190000
PubChem Substance ID:
329753224
grade:
HPLC grade
technique(s):
HPLC: suitable
bp:
55-56 °C (lit.)
55-56 °C
vapor pressure:
4.05 psi ( 20 °C)

grade

HPLC grade

vapor density

3.1 (vs air)

vapor pressure

4.05 psi ( 20 °C)

Assay

99.8%

form

liquid

autoignition temp.

705 °F

purified by

glass distillation

expl. lim.

15.1 %

technique(s)

HPLC: suitable

impurities

<0.010% water

evapn. residue

<0.0003%

refractive index

n20/D 1.369 (lit.)

bp

55-56 °C (lit.)
55-56 °C

density

0.74 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 210 nm Amax: 1.00
λ: 230 nm Amax: 0.40
λ: 250 nm Amax: 0.10
λ: 320-400 nm Amax: 0.01

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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Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H315

Hazard Classifications

Flam. Liq. 2 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

-18.4 °F - closed cup

Flash Point(C)

-28 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
00503AW
08309HW
01608JV
00706BX
00323CX

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Carotenoid Extraction and Quantification from Capsicum annuum.
Richins RD, et al.
Bio-protocol, 4(19), e1256-e1256 (2014)
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.
Torsten C Schmidt et al.
Journal of contaminant hydrology, 70(3-4), 173-203 (2004-05-12)
The fate of fuel oxygenates such as methyl tert-butyl ether (MTBE) in the subsurface is governed by their degradability under various redox conditions. The key intermediate in degradation of MTBE and ethyl tert-butyl ether (ETBE) is tert-butyl alcohol (TBA) which
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