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Merck
모든 사진(2)

주요 문서

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244325

Sigma-Aldrich

2-Iodobutane

≥98%, contains copper as stabilizer

동의어(들):

sec-Butyl iodide

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모든 사진(2)

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 코드:
12352100
PubChem Substance ID:
24854666
NACRES:
NA.22

Quality Level

100

분석

≥98%

양식

liquid

포함

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.)

작용기

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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일반 설명

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.

픽토그램

Flame
GHS02

신호어

Warning

유해 및 위험 성명서

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

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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시험 성적서(COA)

Lot/Batch Number
MKBF3346
MKBC7949
MKBC7176
01401KJ
01325DJ

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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
Ying Wang et al.
Nature communications, 10(1), 5395-5395 (2019-12-05)
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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