推荐产品
化驗
98%
形狀
liquid
折射率
n20/D 1.417 (lit.)
bp
65-66 °C (lit.)
密度
0.87 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
C=CC1CO1
InChI
1S/C4H6O/c1-2-4-3-5-4/h2,4H,1,3H2
InChI 密鑰
GXBYFVGCMPJVJX-UHFFFAOYSA-N
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訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
-58.0 °F - closed cup
閃點(°C)
-50 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Mutation research, 664(1-2), 69-76 (2009-05-12)
The toxicity of butadiene and styrene is exerted by their metabolites. Such metabolites have been extensively scrutinized at the in vitro level demonstrating evident genotoxic properties. In monitoring, a diverse range of outcomes has been produced. Additionally, epidemiological studies in
Stereoselective ring expansion of vinyl oxiranes: mechanistic insights and natural product total synthesis.
Angewandte Chemie (International ed. in English), 49(9), 1648-1651 (2010-02-06)
Journal of the American Chemical Society, 135(4), 1471-1475 (2013-01-01)
Density functional theory computations of the Cu-catalyzed ring expansion of vinyloxiranes is mediated by a traceless dual Cu(I)-catalyst mechanism. Overall, the reaction involves a monomeric Cu(I)-catalyst, but a single key step, the Cu migration, requires two Cu(I)-catalysts for the transformation.
Chemico-biological interactions, 135-136, 703-713 (2001-06-09)
(1-Chloroethenyl)oxirane (CEO) is a metabolite of beta-chloroprene (2-chloro-1,3-butadiene, CD). The purpose of this study was to evaluate the in vitro mutagenic and clastogenic (chromosome breaking) potential of CEO. For comparative purposes, the study also included an evaluation of the racemic
Some insights into the mode of action of butadiene by examining the genotoxicity of its metabolites.
Chemico-biological interactions, 166(1-3), 132-139 (2006-05-16)
1,3-Butadiene (BTD) is an important commodity chemical and air pollutant that has been shown to be a potent carcinogen in mice, and to a lesser extent, a carcinogen in rats. To better assess butadiene's carcinogenic risk to humans, it is
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