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vapor density
2.6 (vs air)
vapor pressure
12.5 mmHg ( 20 °C)
Assay
≥99%
expl. lim.
9.8 %
refractive index
n20/D 1.397 (lit.)
bp
98 °C (lit.)
mp
−115 °C (lit.)
density
0.808 g/mL at 25 °C (lit.)
SMILES string
CCC(C)O
InChI
1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3
InChI key
BTANRVKWQNVYAZ-UHFFFAOYSA-N
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Archives of biochemistry and biophysics, 574, 36-48 (2015-01-21)
Chlorite dismutase-like proteins are structurally closely related to functional chlorite dismutases which are heme b-dependent oxidoreductases capable of reducing chlorite to chloride with simultaneous production of dioxygen. Chlorite dismutase-like proteins are incapable of performing this reaction and their biological role
Anesthesia and analgesia, 103(1), 86-91 (2006-06-23)
Chirality has been proposed as a means for distinguishing relevant from irrelevant molecular targets of action, but the sensitivity and specificity of this test is unknown for volatile anesthetics. We applied enantiomers of two chiral anesthetic alcohols (2-butanol and 2-pentanol)
The journal of physical chemistry. B, 110(29), 14436-14443 (2006-07-21)
In this article, we investigate vapor-liquid-liquid equilibria (VLLE) of binary systems using a simple volumetric method. Being different from the usual cloud-point method for the determination of liquid-liquid separation boundaries, the present volumetric method is able to determine the direct
Tantalum compounds as heterogeneous catalysts for saccharide dehydration to 5-hydroxymethylfurfural.
Chemical communications (Cambridge, England), 47(15), 4469-4471 (2011-03-04)
A new solid acid, based on tantalum hydroxide, was used to catalyze saccharide dehydration into 5-hydroxymethylfurfural (HMF) with high catalytic activity and excellent stability in a water-2-butanol biphasic system. Furthermore, good results were also obtained from Jerusalem artichoke juice with
Journal of the American Chemical Society, 129(49), 15240-15249 (2007-11-16)
The enantioselective chemisorption of R- and S-propylene oxide has been measured either on clean Pd(111) that has been exposed to S-2-butanol at various temperatures to vary the proportion of 2-butanol and 2-butoxide species or by adsorbing S-2-butanol on oxygen-covered Pd(111)
Chromatograms
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