推荐产品
等级
SAJ first grade
蒸汽密度
3 (20 °C, vs air)
蒸汽压
73 mmHg ( 20 °C)
检测方案
≥99.0%
形式
liquid
自燃温度
801 °F
expl. lim.
2.2-11.5 %, 38 °F
存货情况
available only in Japan
折射率
n20/D 1.3720 (lit.)
bp
76.5-77.5 °C (lit.)
mp
−84 °C (lit.)
密度
0.902 g/mL at 25 °C (lit.)
格式
neat
SMILES字符串
CCOC(C)=O
InChI
1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
InChI key
XEKOWRVHYACXOJ-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
危险分类
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
靶器官
Central nervous system
补充剂危害
WGK
WGK 1
闪点(°F)
24.8 °F
闪点(°C)
-4 °C
法规信息
新产品
Junwei Liu et al.
Planta, 241(6), 1435-1451 (2015-02-27)
Strigolactone changes and cross talk with ABA unveil a picture of root-specific hormonal dynamics under stress. Strigolactones (SLs) are carotenoid-derived hormones influencing diverse aspects of development and communication with (micro)organisms, and proposed as mediators of environmental stimuli in resource allocation
K J S Anand et al.
British journal of anaesthesia, 101(5), 680-689 (2008-08-30)
Relationships between plasma morphine concentrations and neonatal responses to endotracheal tube (ETT) suctioning are unknown in preterm neonates. Ventilated preterm neonates (n=898) from 16 centres were randomly assigned to placebo (n=449) or morphine (n=449). After an i.v. loading dose (100
Yuusuke Fujimoto et al.
PloS one, 7(11), e48685-e48685 (2012-11-13)
Combination therapy with ribavirin, interferon, and viral protease inhibitors could be expected to elicit a high level of sustained virologic response in patients infected with hepatitis C virus (HCV). However, several severe side effects of this combination therapy have been
Tsukasa Horiyama et al.
PloS one, 9(9), e108642-e108642 (2014-09-27)
Escherichia coli produces the iron-chelating compound enterobactin to enable growth under iron-limiting conditions. After biosynthesis, enterobactin is released from the cell. However, the enterobactin export system is not fully understood. Previous studies have suggested that the outer membrane channel TolC
Maarit Neuvonen et al.
PloS one, 9(8), e103743-e103743 (2014-08-27)
Bacterial cholesterol oxidase is commonly used as an experimental tool to reduce cellular cholesterol content. That the treatment also generates the poorly degradable metabolite 4-cholesten-3-one (cholestenone) has received less attention. Here, we investigated the membrane partitioning of cholestenone using simulations
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