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Merck

124052

Sigma-Aldrich

溴乙烷

reagent grade, 98%

别名:

乙基溴

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About This Item

经验公式(希尔记法):
C2H5Br
CAS号:
分子量:
108.97
Beilstein:
1209224
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.21

等級

reagent grade

品質等級

蒸汽密度

~3.75 (vs air)

蒸汽壓力

25.32 psi ( 55 °C)
7.54 psi ( 20 °C)

化驗

98%

形狀

liquid

自燃溫度

952 °F

expl. lim.

11.25 %

折射率

n20/D 1.425 (lit.)

bp

37-40 °C (lit.)

mp

−119 °C (lit.)

密度

1.46 g/mL at 25 °C (lit.)

SMILES 字串

CCBr

InChI

1S/C2H5Br/c1-2-3/h2H2,1H3

InChI 密鑰

RDHPKYGYEGBMSE-UHFFFAOYSA-N

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一般說明

Bromoethane (Ethyl bromide) is an alkyl halide. Microwave spectral investigations of ethyl bromide and its isotopic species have been reported. It has been synthesized either by employing Grignard waste water as a precursor3 or by reacting potassium bromide with concentrated sulfuric acid in ethanol.

應用

Bromoethane may be employed as a promoter during the preparation of 1-butene.4 It has been used to prepare anion-exchange membranes, which can be used for the isolation and purification of plasmid DNA and also for the separation of plasmid DNA and RNA from cell lysates, measured using ultraviolet-visible light spectrophotometer.

訊號詞

Danger

危險分類

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 2 - Ozone 1

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

-9.4 °F - closed cup

閃點(°C)

-23 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves


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分析证书(COA)

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"Preparation of inorganic?organic anion-exchange membranes and their application in plasmid DNA and RNA separation"
Chang S-C, et al.
Journal of Membrane Science, 311(1), 336-348 (2008)
Ramsden.N.E et al.
A-Level Chemistry (2000)
Microwave Spectrum, Structure, and Quadrupole Coupling Constant Tensor of Ethyl Bromide.
Flanagan C and Pierce L.
J. Chem. Phys. , 38(12), 2963-2969 (1963)
Paula Teper-Bamnolker et al.
Plant physiology, 158(4), 2053-2067 (2012-03-01)
Potato (Solanum tuberosum) tuber, a swollen underground stem, is used as a model system for the study of dormancy release and sprouting. Natural dormancy release, at room temperature, is initiated by tuber apical bud meristem (TAB-meristem) sprouting characterized by apical
J R Bucher et al.
Toxicology and applied pharmacology, 130(1), 169-173 (1995-01-01)
Chloroethane and bromoethane have been shown to cause a marked uterine tumor response in B6C3F1 mice exposed for 2 years. These chemicals are nearly unique in this regard among the nearly 400 chemicals studied by the National Toxicology Program, and

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