1.01995

tert-Butyl methyl ether

for gas chromatography ECD and FID SupraSolv^®

• Synonyme(s) : tert-Butyl methyl ether, MTBE, MTB, 2-Methoxy-2-methylpropane, Methyl tert-butyl ether
• Formule linéaire : (CH₃)₃COCH₃
• Numéro CAS: 1634-04-4
• Poids moléculaire : 88.15
• Numéro MDL: MFCD00008812
• Code UNSPSC : 12191502
• Numéro de classement CE : 216-653-1
• Nomenclature NACRES : NA.03

Propriétés

• Pression de vapeur: 268 hPa ( 20 °C)
• Niveau de qualité: 100
• Gamme de produits: SupraSolv^®
• Pureté: ≥99.8% (GC)
• Forme: liquid
• Température d'inflammation spontanée: 460 °C
• Puissance: >2000 mg/kg LD₅₀, oral (Rat); >2000 mg/kg LD₅₀, skin (Rabbit)
• Limite d'explosivité: 1.5-8.5 % (v/v)
• Technique(s): gas chromatography (GC): suitable
• kinematic viscosity: 0.409 cSt(40 °C)
• Point d'ébullition: 55.3 °C/1013 hPa
• Pf: -108.6 °C
• Température de transition: flash point -28 °C
• Densité: 0.74 g/cm³ at 20 °C
• Température de stockage: 2-30°C
• InChI: 1S/C5H12O/c1-5(2,3)6-4/h1-4H3
• Clé InChI: BZLVMXJERCGZMT-UHFFFAOYSA-N

Description

Description générale

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).

Autres remarques

Explore various lab safety accessories and equipment for safe handling of solvents to increase your safety level from the first usage.

Informations légales

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

Informations sur la sécurité

• Pictogrammes: GHS02,GHS07
• Mention d'avertissement: Danger
• Mentions de danger: H225 - H315
• Conseils de prudence: P210 - P233 - P240 - P241 - P242 - P303 + P361 + P353
• Classification des risques: Flam. Liq. 2 - Skin Irrit. 2
• Code de la classe de stockage: 3 - Flammable liquids
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): -18.4 °F - closed cup
• Point d'éclair (°C): -28 °C - closed cup