1.01995

tert-Butyl methyl ether

for gas chromatography ECD and FID SupraSolv^®

• Synonym(s): tert-Butyl methyl ether, MTBE, MTB, 2-Methoxy-2-methylpropane, Methyl tert-butyl ether
• Linear Formula: (CH₃)₃COCH₃
• CAS Number: 1634-04-4
• Molecular Weight: 88.15
• MDL number: MFCD00008812
• UNSPSC Code: 12191502
• EC Index Number: 216-653-1
• NACRES: NA.03

Properties

• vapor pressure: 268 hPa ( 20 °C)
• Quality Level: 100
• 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
• InChI: 1S/C5H12O/c1-5(2,3)6-4/h1-4H3
• InChI key: BZLVMXJERCGZMT-UHFFFAOYSA-N

Description

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

Safety Information

• Pictograms: GHS02,GHS07
• Signal Word: Danger
• Hazard Statements: H225 - H315
• Precautionary Statements: P210 - P233 - P240 - P241 - P242 - P303 + P361 + P353
• 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