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1.01843

tert-Butyl methyl ether

EMPLURA®

Synonyme(s) :

tert-Butyl methyl ether, Methyl tert-butyl ether, MTB, MTBE

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A propos de cet article

Formule linéaire :
(CH3)3COCH3
Numéro CAS:
Poids moléculaire :
88.15
UNSPSC Code:
12191502
EC Index Number:
216-653-1
NACRES:
NA.05
MDL number:
Assay:
≥99% (GC)
Bp:
55.3 °C/1013 hPa
Vapor pressure:
268 hPa ( 20 °C)
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vapor pressure

268 hPa ( 20 °C)

Quality Level

product line

EMPLURA®

assay

≥99% (GC)

form

liquid

autoignition temp.

460 °C

potency

>2000 mg/kg LD50, oral (Rat), >2000 mg/kg LD50, skin (Rabbit)

expl. lim.

1.5-8.5 % (v/v)

dilution

(low-cost alternative, for basic applications)

impurities

≤0.001% Free acid (as CH3COOH), ≤0.005% Peroxide (as H2O2), ≤0.05% Water

evapn. residue

≤0.005%

kinematic viscosity

0.464 cSt(20 °C)

bp

55.3 °C/1013 hPa

mp

-108.6 °C

transition temp

flash point -28 °C

solubility

42 g/L

density

0.74 g/cm3 at 20 °C

storage temp.

2-30°C

SMILES string

O(C(C)(C)C)C

InChI

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

InChI key

BZLVMXJERCGZMT-UHFFFAOYSA-N

General description

EMPLURA® is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and cleaning purposes. EMPLURA solvents provide adequate specifications with the most important parameters.

Application


  • Evidence for HOOO radicals in the formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the ozonation of C-H bonds in hydrocarbons.: This research used tert-Butyl methyl ether to investigate the formation of hydrotrioxides and hydrogen trioxide in the ozonation of hydrocarbons, providing insights into radical chemistry and ozonation processes (Cerkovnik et al., 2002).

  • Determination of ochratoxin A in baby food by immunoaffinity column cleanup with liquid chromatography: interlaboratory study.: The study employed tert-Butyl methyl ether in the cleanup process for detecting ochratoxin A in baby food, demonstrating its effectiveness in ensuring food safety through reliable analytical methods (Burdaspal et al., 2001).

  • Sensitive high-performance liquid chromatography/mass spectrometry method for determination of steviol in rat plasma.: This paper highlights the use of tert-Butyl methyl ether in developing a sensitive HPLC/MS method for analyzing steviol in biological samples, showcasing its application in pharmacokinetic and toxicological studies (Wang et al., 2004).

  • Comparative fatty acid selectivity of lipases in esterification reactions with glycerol and diol analogues in organic media.: The research employed tert-Butyl methyl ether to investigate lipase selectivity in esterification reactions, illustrating its importance in biocatalysis and industrial applications of enzymatic processes (Lee & Parkin, 2000).

  • Analysis of coumarin 7-hydroxylation activity of cytochrome P450 2A6 using random mutagenesis.: This study utilized tert-Butyl methyl ether to analyze enzyme activity in cytochrome P450, demonstrating its utility in biochemical assays and the study of enzyme kinetics (Kim et al., 2005).

Analysis Note

Purity (GC): ≥ 99.0 %
Identity (IR): conforms
Free acid (as CH₃COOH): ≤ 0.001 %
Density (d 20 °C/ 4 °C): 0.740 - 0.742
Peroxide (as H₂O₂): ≤ 0.005 %
Evaporation residue: ≤ 0.005 %
Water: ≤ 0.05 %

Legal Information

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


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Danger

hcodes

Hazard Classifications

Flam. Liq. 2 - Skin Irrit. 2

Classe de stockage

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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Numéro d'article de commerce international

RéférenceGTIN
101843052104061838825100
101843250104061838825117
101843602504022536025551
101843901104027269350628
101843050104061838825094
101843250004022536025537
101843252104061838825124
101843619004022536025568
101843902704061838825131