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
Beilstein:
1718777
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥98%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.499 (lit.)
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
SMILES string
CCC(C)I
InChI
1S/C4H9I/c1-3-4(2)5/h4H,3H2,1-2H3
InChI key
IQRUSQUYPCHEKN-UHFFFAOYSA-N
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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.
accessory
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
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
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Frank Keppler et al.
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Synthesis of higher carboxylic acids using CO2 and H2 is of great importance, because CO2 is an attractive renewable C1 resource and H2 is a cheap and clean reductant. Herein we report a route to produce higher carboxylic acids via
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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