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About This Item
Linear Formula:
C2H5CH(OH)CH3
CAS Number:
Molecular Weight:
74.12
Beilstein:
1718763
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
vapor density
2.6 (vs air)
Quality Level
vapor pressure
12.5 mmHg ( 20 °C)
Assay
99%
form
liquid
optical activity
[α]20/D +13°, neat
autoignition temp.
761 °F
expl. lim.
9.8 %
refractive index
n20/D 1.397 (lit.)
bp
99-100 °C (lit.)
density
0.803 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CC[C@H](C)O
InChI
1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3/t4-/m0/s1
InChI key
BTANRVKWQNVYAZ-BYPYZUCNSA-N
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Application
(S)-(+)-2-Butanol can be used:
- To synthesize chiral asymmetric perylene diimides (PDI) that spontaneously self-assemble into one-handed nanotubes that are photoconductive or fluorescent in nature.
- To synthesize bulky chiral vinyl monomers that can be radically polymerized to helical polymers with an excess screw sense.
- As chiral solvent to study excited state photo transfer of the photoacid, 5,8-dicyano-2-naphthol (DCN2) in chiral environment.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3
Target Organs
Central nervous system, Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
75.2 °F - closed cup
Flash Point(C)
24 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Highly fluorescent one-handed nanotubes assembled from a chiral asymmetric perylene diimide.
Ma X , et al.
Chemical Communications (Cambridge, England), 51(20), 4231-4233 (2015)
Excited-state proton transfer in chiral environments. 1. Chiral solvents.
Solntsev KM, et al.
Journal of the American Chemical Society, 124(31), 9046-9047 (2002)
Synthesis and characterization of optically active helical vinyl polymers via free radical polymerization.
Zhi J, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 47(9), 2408-2421 (2009)
Stepwise Formation of Photoconductive Nanotubes through a New Top?Down Method.
Ma X , et al.
Advanced Materials, 27(47), 7746-7751 (2015)
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
Chromatograms
suitable for GC
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