30-0930
Tetrahydrofuran
≥99.7% (GC), contains no stabilizer, suitable for HPLC
Synonym(s):
THF, Butylene oxide, Oxolane, Tetramethylene oxide
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About This Item
Empirical Formula (Hill Notation):
C4H8O
CAS Number:
Molecular Weight:
72.11
Beilstein:
102391
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
Recommended Products
product name
Tetrahydrofuran, suitable for HPLC, contains no stabilizer
vapor density
2.5 (vs air)
vapor pressure
114 mmHg ( 15 °C)
143 mmHg ( 20 °C)
Assay
≥99.7% (GC)
form
liquid
autoignition temp.
610 °F
does not contain
stabilizer
expl. lim.
1.8-11.8 %
availability
available only in Japan
technique(s)
HPLC: suitable
refractive index
n20/D 1.407 (lit.)
pH
~7
bp
65-67 °C (lit.)
mp
−108 °C (lit.)
density
0.889 g/mL at 25 °C (lit.)
SMILES string
C1CCOC1
InChI
1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI key
WYURNTSHIVDZCO-UHFFFAOYSA-N
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Application
- Complexation and disproportionation of group 4 metal (alkoxy) halides with phosphine oxides.: This research utilizes tetrahydrofuran (THF) as a solvent to study the complexation and disproportionation reactions of group 4 metal halides, providing insights into coordination chemistry and potential applications in materials science (Seno et al., 2024).
- Synthesis of Room Temperature Curable Polymer Binder Mixed with Polymethyl Methacrylate and Urethane Acrylate for High-Strength and Improved Transparency.: THF is used as a solvent in the synthesis of advanced polymer binders, highlighting its role in developing materials with enhanced mechanical properties and optical clarity for industrial applications (Lee et al., 2024).
- Fabrication of Polypyrrole Hollow Nanospheres by Hard-Template Method for Supercapacitor Electrode Material.: This study employs THF in the fabrication process of polypyrrole nanospheres, demonstrating its importance in the production of high-performance supercapacitor electrode materials (Hong et al., 2024).
- Promoting Cross-Link Reaction of Polymers by the Matrix-Filler Interface Effect: Role of Coupling Agents and Intermediate Linkers.: The use of THF as a solvent facilitates the cross-linking reactions in polymers, enhancing their mechanical stability and expanding their applications in various fields of materials science (Huang et al., 2024).
- Solvent Regulation Induced Cathode Aggregation-Induced Electrochemiluminescence of Tetraphenylethylene Nanoaggregates for Ultrasensitive Zearalenone Analysis.: THF is critical in the solvent regulation process for electrochemiluminescence assays, significantly improving the sensitivity of analytical techniques for detecting environmental contaminants (Chen et al., 2024).
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Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
Target Organs
Central nervous system, Respiratory system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
5.9 °F
Flash Point(C)
-14.5 °C
Certificates of Analysis (COA)
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Ryan D Pensack et al.
Journal of the American Chemical Society, 137(21), 6790-6803 (2015-05-07)
We compare the singlet fission dynamics of five pentacene derivatives precipitated to form nanoparticles. Two nanoparticle types were distinguished by differences in their solid-state order and kinetics of triplet formation. Nanoparticles that comprise primarily weakly coupled chromophores lack the bulk
Luca Chiari et al.
The Journal of chemical physics, 138(7), 074301-074301 (2013-03-01)
We present total, elastic, and inelastic cross sections for positron and electron scattering from tetrahydrofuran (THF) in the energy range between 1 and 5000 eV. Total cross sections (TCS), positronium formation cross sections, the summed inelastic integral cross sections (ICS)
Han Yan et al.
Advanced materials (Deerfield Beach, Fla.), 27(23), 3484-3491 (2015-05-06)
Polymer solar cells are fabricated with systematic variation of the phase purity. Photovoltaic tests demonstrate that devices with ca. 10% of mixed phases outperform pure-phase devices. Photophysical studies reveal the effects of mixed phase on charge generation and recombination. These
Crispin Lichtenberg et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(44), 15797-15805 (2015-09-17)
The reactivity of the all-ferrous FeN heterocubane [Fe4 (Ntrop)4 ] (1) with i) Brønsted acids, ii) σ-donors, iii) σ-donors/π-acceptors, and iv) one-electron oxidants has been investigated (trop = 5H-dibenzo[a,d]cyclo-hepten-5-yl). 1 showed self-re-assembling after reactions with i) and proved surprisingly inert in reactions with ii)
C N Ong et al.
British journal of industrial medicine, 48(9), 616-621 (1991-09-01)
Occupational exposure to tetrahydrofuran (THF) was studied by analysis of environmental air, blood, alveolar air, and urine from 58 workers in a video tape manufacturing plant. Head space gas chromatography (GC) with an FID detector was used for determination of
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