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Acerca de este artículo
Fórmula lineal:
(CH3)3COCH3
Número CAS:
Peso molecular:
88.15
EC Number:
216-653-1
UNSPSC Code:
12190000
PubChem Substance ID:
Beilstein/REAXYS Number:
1730942
MDL number:
En este momento no podemos mostrarle ni los precios ni la disponibilidad
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlevapor density
3.1 (vs air)
grade
puriss.
assay
≥99.5% (GC)
autoignition temp.
705 °F
quality
dried over molecular sieve (H2O ≤0.01%)
expl. lim.
15.1 %
impurities
≤0.01% water
refractive index
n20/D 1.369
bp
55-56 °C (lit.)
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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signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - Skin Irrit. 2
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-18.4 °F - closed cup
flash_point_c
-28 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
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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

