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Merck
CN

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:
513-48-4
Molecular Weight:
184.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854666
EC Number:
208-163-1
Beilstein/REAXYS Number:
1718777
MDL number:
MFCD00001072
Assay:
≥98%
Form:
liquid

Key Documents

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Product Name

2-Iodobutane, ≥98%, contains copper as stabilizer

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

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
iodo

Quality Level

100

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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.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCW1952
MKCS1240
MKCS4165
MKCR7355
MKBF3346

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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
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.
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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