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重要文件

244325

Sigma-Aldrich

2-碘丁烷

≥98%, contains copper as stabilizer

同義詞:

仲丁基碘

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About This Item

線性公式:
CH3CH2CHICH3
CAS號碼:
分子量::
184.02
Beilstein:
1718777
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥98%

形狀

liquid

包含

copper as stabilizer

折射率

n20/D 1.499 (lit.)

bp

119-120 °C (lit.)

mp

−104 °C (lit.)

溶解度

alcohol: soluble(lit.)
diethyl ether: soluble(lit.)
water: insoluble(lit.)

密度

1.598 g/mL at 25 °C (lit.)

官能基

alkyl halide
iodo

SMILES 字串

CCC(C)I

InChI

1S/C4H9I/c1-3-4(2)5/h4H,3H2,1-2H3

InChI 密鑰

IQRUSQUYPCHEKN-UHFFFAOYSA-N

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一般說明

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.

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

75.2 °F - closed cup

閃點(°C)

24 °C - closed cup

個人防護裝備

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


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分析證明 (COA)

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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
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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