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2-Methyltetrahydrofuran, 99%, stab. with ca 150-400ppm BHT, Thermo Scientific Chemicals
製品番号（カタログ番号）： L07356.AP
500 mL, Each
化学物質識別子
CAS
96-47-9
IUPAC Name
2-methyloxolane
Molecular Formula
C5H10O
InChI Key
JWUJQDFVADABEY-UHFFFAOYNA-N
SMILES
CC1CCCO1
仕様
スペックシートAppearance (Color)
Clear colorless
Form
Liquid
Assay (GC)
≥98.5% (non-U.S. specification)
Assay from Suppliers CofA
≥98.5% (U.S. specification)
Comment
Specification differs for U.S. and non-U.S. material where indicated
概要
2-Methyltetrahydrofuran acts as a solvent in organic synthesis. It is considered as a replacement for terahydrofuran due to its higher reaction temperature and easy separation after reaction. It is also useful in the electrolyte formulation for secondary lithium electrodes and as a component in alternative fuels. Further, it is used as a solvent for spectroscopic studies at -1960C. It also acts as a solvent for Grignard reagent in organometallic reactions. In addition to this, it plays an important role as a motor fuel.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Methyltetrahydrofuran acts as a solvent in organic synthesis. It is considered as a replacement for terahydrofuran due to its higher reaction temperature and easy separation after reaction. It is also useful in the electrolyte formulation for secondary lithium electrodes and as a component in alternative fuels. Further, it is used as a solvent for spectroscopic studies at -1960C. It also acts as a solvent for Grignard reagent in organometallic reactions. In addition to this, it plays an important role as a motor fuel.
Solubility
Miscible with water and most organic solvents.
Notes
Incompatible with oxidizing agents, strong acids and strong bases.
2-Methyltetrahydrofuran acts as a solvent in organic synthesis. It is considered as a replacement for terahydrofuran due to its higher reaction temperature and easy separation after reaction. It is also useful in the electrolyte formulation for secondary lithium electrodes and as a component in alternative fuels. Further, it is used as a solvent for spectroscopic studies at -1960C. It also acts as a solvent for Grignard reagent in organometallic reactions. In addition to this, it plays an important role as a motor fuel.
Solubility
Miscible with water and most organic solvents.
Notes
Incompatible with oxidizing agents, strong acids and strong bases.
RUO – Research Use Only
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