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About This Item
Linear Formula:
CH3CH2CH(OH)CH3
CAS Number:
Molecular Weight:
74.12
Beilstein:
773649
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
Recommended Products
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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Stefan Hofbauer et al.
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
Robert Brosnan et al.
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)
Ravi K Pathak et al.
Environmental science & technology, 46(21), 11660-11669 (2012-09-19)
Limonene has a strong tendency to form secondary organic aerosol (SOA) in the atmosphere and in indoor environments. Initial oxidation occurs mainly via ozone or OH radical chemistry. We studied the effect of O(3) concentrations with or without a OH
Feng Gao et al.
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)
Flaminia Rondino et al.
Physical chemistry chemical physics : PCCP, 13(3), 818-824 (2010-12-07)
Diastereomeric adducts between (S)-1-(4-fluorophenyl)-ethanol and R and S 2-butanol, formed by supersonic expansion, have been investigated by means of a combination of mass selected resonant two-photon ionization-spectroscopy and infrared depletion spectroscopy. Chiral recognition is evidenced by the specific spectroscopic signatures
Chromatograms
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