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Thermo Scientific Chemicals
Tetrahydrofuran, 99%, stab. with 250-350ppm BHT
CAS: 109-99-9 | C4H8O | 72.11 g/mol
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化學識別
CAS109-99-9
IUPAC Nameoxolane
Molecular FormulaC4H8O
InChI KeyWYURNTSHIVDZCO-UHFFFAOYSA-N
SMILESC1CCOC1
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規格
規格表
規格表Water Content (Karl Fischer Titration)≤0.05%
Assay (GC)≥98.5%
Refractive Index1.4055-1.4085 @ 20?C
Identification (FTIR)Conforms
FormLiquid
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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
Tetrahydrofuran is used as a solvent in Grignard reagent formation processes, pharmaceutical steroids and in the preparation of organometallic reagents. It is used for HPLC, spectrophotometry and environmental testing. It is used as a resin solvent in flexographic inks for plastics coating deposition for audio and video tapes. It is used in PVC and CPVC pipe cements, polyurethane coatings and in PVC film castings.
Solubility
Miscible with water.
Notes
Highly flammable. Oxidizes readily in air to form unstable peroxides. THF exhibits high volatility and an extremely low freezing point. Keep the container tightly closed and sealed until ready for use.
Tetrahydrofuran is used as a solvent in Grignard reagent formation processes, pharmaceutical steroids and in the preparation of organometallic reagents. It is used for HPLC, spectrophotometry and environmental testing. It is used as a resin solvent in flexographic inks for plastics coating deposition for audio and video tapes. It is used in PVC and CPVC pipe cements, polyurethane coatings and in PVC film castings.
Solubility
Miscible with water.
Notes
Highly flammable. Oxidizes readily in air to form unstable peroxides. THF exhibits high volatility and an extremely low freezing point. Keep the container tightly closed and sealed until ready for use.
RUO – Research Use Only
- Hu, X.; Wang, S.; Westerhof, R. J. M.; Wu, L.; Song, Y.; Dong, D.; Li, C. Z. Acid-catalyzed conversion of C6 sugar monomer/oligomers to levulinic acid in water, tetrahydrofuran and toluene: Importance of the solvent polarity. Fuel 2015, 141, 56-63.
- Šach, R.; Štěpánek, M.; Procházka, K. Fluorescence Study of the Solvation of Fluorescent Probes Prodan and Laurdan in Poly(ε-caprolactone)-block-poly(ethylene oxide) Vesicles in Aqueous Solutions with Tetrahydrofurane. Langmuir 2008, 24, (1), 288-295.
- Wu, J-Y.; Chen, L-J.; Chen, Y-P.; Lin, S-T. Molecular Dynamics Study on the Equilibrium and Kinetic Properties of Tetrahydrofuran Clathrate Hydrates. J. Phys. Chem. C. 2015, 119 (3), 1400-1409.
- Sugimura, H.; Sato, S.; Tokudome, K.; Yamada, T. Stereoselective Formation of Tetrahydrofuran Rings via [3 + 2] Annulation: Total Synthesis of Plakortone L. Org. Lett. 2014, 16 (12), 3384-3387.