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244325

Sigma-Aldrich

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
Beilstein:
1718777
EC Number:
208-163-1
MDL number:
MFCD00001072
UNSPSC Code:
12352100
PubChem Substance ID:
24854666
NACRES:
NA.22

Quality Level

100

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

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

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

244325-500G:
244325-100G:4548173987279
244325-5G:4548173987262
244325-BULK:
244325-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
U4345
MKCW1952
U6260
U7167
MKCS1240

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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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