Sigma-Aldrich 401757 Tetrahydrofuran anhydrous, ≥99.9%, inhibitor-free 20 L
Category
Brand
Stock Code
LB.SA.401757-20L
Kısa Bilgi
Synonym(s): THF, Butylene oxide, Oxolane, Tetramethylene oxide Empirical Formula (Hill Notation): C4H8O CAS Number: 109-99-9 Molecular Weight: 72.11 Beilstein: 102391 EC Number: 203-726-8 MDL number: MFCD00005356 PubChem Substance ID: 57649919 NACRES: NA.21
| Sigma-Aldrich 401757 Tetrahydrofuran anhydrous, ≥99.9%, inhibitor-free 20 L |
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Synonym(s): THF, Butylene oxide, Oxolane, Tetramethylene oxide
Empirical Formula (Hill Notation): C4H8O
CAS Number: 109-99-9
Molecular Weight: 72.11
Beilstein: 102391
EC Number: 203-726-8
MDL number: MFCD00005356
PubChem Substance ID: 57649919
NACRES: NA.21
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PROPERTIES
grade anhydrous
Quality Level 200
vapor density 2.5 (vs air)
vapor pressure 114 mmHg ( 15 °C) 143 mmHg ( 20 °C)
assay ≥99.9%
form liquid
autoignition temp. 610 °F
expl. lim. 1.8-11.8 %
impurities
≤20 ppm peroxide (as H2O2)
<0.002% water
<0.005% water (100 mL pkg)
evapn. residue <0.0005%
refractive index n20/D 1.407 (lit.)
pH ~7
bp 65-67 °C (lit.)
mp −108 °C (lit.)
solubility H2O: soluble
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
DESCRIPTION
General description
Tetrahydrofuran (THF) is a saturated cyclic ether with a potential use as a biofuel. Its combustion studies have been investigated.[1] Reports suggest that it is a better promoter than 1,3 dioxolane for CO2-hydrate formation.[2] Application Tetrahydrofuran was used as a solvent in the formation of diacetylinic polymers.[3] It may be used in the following processes: Formation of butyrolactone (BTL) by green oxidation method.[4] Aqueous THF solution to modify the polystyrene surface by swelling process.[5] As a solvent for lignin depolymerization to isolate phenolic monomer.[6]
Packaging
100, 12×100 mL in Sure/Seal™
1, 6×1, 2, 4×2 L in Sure/Seal™
18 L in Pure-Pac™
1 20, 50 L in Pure-Pac™ 2
56 L in Pure-Pac™ 1
200 L in Pure-Pac™ 2
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