Tetrahydrofuran
From Free net encyclopedia
Tetrahydrofuran | |
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Image:THF chemical structure.png | |
General | |
Systematic name | Tetrahydrofuran |
Other names | THF, hydrofuran, oxolane, oxacyclopentane, furanidine |
Molecular formula | C4H8O |
SMILES | C1CCCO1 |
Molar mass | 72.11 g/mol |
Appearance | colorless liquid |
CAS number | [109-99-9] |
Properties | |
Density and phase | 0.886 g/cm3, liquid |
Solubility in water | Miscible |
Melting point | -108.4 °C (164.75 K) |
Boiling point | 66 °C (339.15 K) |
Viscosity | 4.856 cP at 25 °C |
Structure | |
Molecular shape | envelope |
Dipole moment | 1.63 D (gas) |
Hazards | |
MSDS | External MSDS |
EU classification | Flammable (F) Irritant (Xi) |
NFPA 704 | Template:Nfpa |
R-phrases | Template:R11, Template:R19, Template:R36/37 |
S-phrases | Template:S2, Template:S9, Template:S16, Template:S23 |
Flash point | -14 °C |
RTECS number | LU5950000 |
Supplementary data page | |
Structure and properties | n, εr, etc. |
Thermodynamic data | Phase behaviour Solid, liquid, gas |
Spectral data | UV, IR, NMR, MS |
Related compounds | |
Related heterocycles | Furan Pyrrolidine Dioxane |
Related compounds | Diethyl ether |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
- For other uses of THF, see THF (disambiguation)
Tetrahydrofuran is a heterocyclic organic compound. It is a clear, low-viscosity liquid with an diethyl ether-like smell. It is one of the most polar ethers and is used as a solvent of intermediate polarity in chemical reactions. THF is an aprotic, electron donating solvent with a dielectric constant of 7.6. THF is the fully hydrogenated analog of the aromatic compound furan.
Contents |
Precautions
THF tends to form peroxides on storage. As a result, THF should not be distilled to dryness, which can leave a residue of highly-explosive peroxides. Commercial THF is therefore often inhibited with BHT. Alternatively, THF can be stored in air-tight bottles in the dark over sodium hydroxide.
External links
- International Chemical Safety Card 0578
- NIOSH Pocket Guide to Chemical Hazards
- Template:Ecb
- THF usage on Organic Syntheses
- THF info
- U.S. OSHA info on THF
References
- Loudon, G. Mark. Organic Chemistry 4th ed. New York: Oxford University Press. 2002. pg 318.
See also
- The Trapp mixture extends the temperature range applicability of THF as a solvent.
Template:Expandde:Tetrahydrofuran fr:Tétrahydrofurane it:Tetraidrofurano lv:THF nl:Tetrahydrofuraan ja:テトラヒドロフラン pl:Tetrahydrofuran zh:四氢呋喃