1.01995
tert-Butyl methyl ether
for gas chromatography ECD and FID SupraSolv®
동의어(들):
tert-Butyl methyl ether, MTBE, MTB, 2-Methoxy-2-methylpropane, Methyl tert-butyl ether
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3)3COCH3
CAS 번호:
Molecular Weight:
88.15
UNSPSC Code:
12191502
EC Index Number:
216-653-1
NACRES:
NA.03
MDL number:
Assay:
≥99.8% (GC)
Technique(s):
gas chromatography (GC): suitable
Bp:
55.3 °C/1013 hPa
Vapor pressure:
268 hPa ( 20 °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
vapor pressure
268 hPa ( 20 °C)
product line
SupraSolv®
assay
≥99.8% (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)
technique(s)
gas chromatography (GC): suitable
kinematic viscosity
0.409 cSt(40 °C)
bp
55.3 °C/1013 hPa
mp
-108.6 °C
transition temp
flash point -28 °C
density
0.74 g/cm3 at 20 °C
storage temp.
2-30°C
Quality Level
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General description
SupraSolv ECD and FID is specially developed for gas chromatography in combination with ECD (Electron Capture Detetor) and FID (Flame Ionization detector). SupraSolv solvents offer the largest specified retention time range, a clear baseline and a minimal signal-to-noise ratio leading to reliable and reproducible analysis results.
Application
- Lipase-catalyzed kinetic resolution of novel antitubercular benzoxazole derivatives.: This study used tert-Butyl methyl ether in the lipase-catalyzed kinetic resolution of benzoxazole derivatives, demonstrating its application in the synthesis of enantiomerically pure compounds important for medicinal chemistry (Łukowska-Chojnacka et al., 2018).
- A chemoenzymatic approach to the synthesis of enantiomerically pure (S)-3-hydroxy-gamma-butyrolactone.: The research developed a chemoenzymatic method using tert-Butyl methyl ether for synthesizing enantiomerically pure compounds, highlighting its utility in producing important chiral building blocks for pharmaceuticals (Lee et al., 2008).
- Determination of roxatidine in human plasma by liquid chromatography/electrospray mass spectrometry and application to a clinical pharmacokinetic study.: This study demonstrated the use of tert-Butyl methyl ether in sample preparation for the analysis of roxatidine in human plasma, emphasizing its role in pharmacokinetic studies (Shin et al., 2007).
- Analysis of coumarin 7-hydroxylation activity of cytochrome P450 2A6 using random mutagenesis.: This paper used tert-Butyl methyl ether in the study of enzyme activity, showing its effectiveness in biochemical assays involving cytochrome P450 enzymes (Kim et al., 2005).
- 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).
Other Notes
Explore various lab safety accessories and equipment for safe handling of solvents to increase your safety level from the first usage.
Legal Information
SUPRASOLV is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2 - Skin Irrit. 2
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-18.4 °F - closed cup
flash_point_c
-28 °C - closed cup
시험 성적서(COA)
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국제 무역 품목 번호
| SKU | GTIN |
|---|---|
| 1.01995.2500 | 04022536027319 |
| 1.01995.1000 | 04022536027296 |
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