244325
2-Iodobutane
≥98%, contains copper as stabilizer
Synonym(s):
sec-Butyl iodide
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About This Item
Linear Formula:
CH3CH2CHICH3
CAS Number:
Molecular Weight:
184.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-163-1
Beilstein/REAXYS Number:
1718777
MDL number:
Assay:
≥98%
Form:
liquid
InChI key
IQRUSQUYPCHEKN-UHFFFAOYSA-N
InChI
1S/C4H9I/c1-3-4(2)5/h4H,3H2,1-2H3
SMILES string
CCC(C)I
assay
≥98%
form
liquid
contains
copper as stabilizer
Quality Level
bp
119-120 °C (lit.)
mp
−104 °C (lit.)
solubility
alcohol: soluble(lit.), diethyl ether: soluble(lit.), water: insoluble(lit.)
density
1.598 g/mL at 25 °C (lit.)
functional group
alkyl halide, iodo
Related Categories
General description
2-Iodobutane was degraded by reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution. The release rate of 2-iodobutane, a volatile organoiodide, was studied.
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
75.2 °F - closed cup
flash_point_c
24 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Frank Keppler et al.
Chemosphere, 52(2), 477-483 (2003-05-10)
Volatile iodinated organic compounds play an important role in the tropospheric photochemical system, but the current knowledge of the known sources and sinks of these alkyl iodides is still incomplete. This paper describes a new source of alkyl iodides from
Kajari Chatterjee et al.
ACS omega, 5(27), 16681-16689 (2020-07-21)
Our society is critically dependent on lithium-ion batteries (LIBs) as a power source for portable electronic gadgets. One of the major problems with these batteries is the degradation of the materials inside them. In addition to the reduced cell life
Kajari Chatterjee et al.
Scientific reports, 10(1), 9606-9606 (2020-06-17)
A novel dicationic room temperature ionic liquid, 1,1'-(5,14-dioxo-4,6,13,15-tetraazaoctadecane-1,18-diyl) bis(3-(sec-butyl)-1H-imidazol-3-ium) bis((trifluoromethyl)-sulfonyl) imide has been synthesized and fully characterized. Its thermal and electrochemical analyses along with transport properties have been studied. We propose it as a potential nominal additive to the commonly
G Lunn et al.
American Industrial Hygiene Association journal, 52(6), 252-257 (1991-06-01)
Two techniques were investigated for degrading a number of halogenated compounds of commercial and research importance. Reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution was used to degrade iodomethane, chloroacetic acid, trichloroacetic acid, 2-chloroethanol, 2-bromoethanol, 2-chloroethylamine, 2-bromoethylamine, 1-bromobutane, 1-iodobutane
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