V001148
Tetrahydrofuran
p.a., 99%
Synonym(s):
Butylene oxide, Oxolane, Tetramethylene oxide
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About This Item
Empirical Formula (Hill Notation):
C4H8O
CAS Number:
Molecular Weight:
72.11
EC Number:
203-726-8
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
102391
vapor pressure
114 mmHg ( 15 °C), 143 mmHg ( 20 °C)
grade
p.a.
assay
99%
autoignition temp.
610 °F
expl. lim.
1.8-11.8 %
mp
−108 °C (lit.)
density
0.889 g/mL at 25 °C (lit.)
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Danger
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-6.2 °F - closed cup
flash_point_c
-21.2 °C - closed cup
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E Vilarrasa et al.
Poultry science, 94(7), 1527-1538 (2015-03-17)
The aim of the present study was to investigate the potential use of re-esterified oils, differing in their degree of saturation and molecular structure, in comparison with their corresponding acid and native oils in broiler chicken diets. For this purpose
Tetrahydrofuran-containing macrolides: a fascinating gift from the deep sea.
Adriana Lorente et al.
Chemical reviews, 113(7), 4567-4610 (2013-03-20)
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
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)
Fabrice Giusti et al.
The Journal of membrane biology, 247(9-10), 909-924 (2014-03-22)
Amphipols are short amphipathic polymers that can substitute for detergents at the hydrophobic surface of membrane proteins (MPs), keeping them soluble in the absence of detergents while stabilizing them. The most widely used amphipol, known as A8-35, is comprised of
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