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蒸汽密度
5.94 (vs air)
方案
97%
折射率
n20/D 1.4322 (lit.)
沸点
109-115 °C/5 mmHg (lit.)
mp
−2 °C (lit.)
密度
0.825 g/mL at 25 °C (lit.)
SMILES字符串
CCCCCCCCCCC=O
InChI
1S/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h11H,2-10H2,1H3
InChI key
KMPQYAYAQWNLME-UHFFFAOYSA-N
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应用
大蜡螟的性信息素。
警示用语：
Warning
危险声明
危险分类
Skin Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
221.0 °F
闪点(°C)
105 °C
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Aldrichimica Acta, 16, 41-41 (1983)
Fangfang Zeng et al.
Insect biochemistry and molecular biology, 113, 103213-103213 (2019-08-24)
Mosquitoes rely heavily on the olfactory system to find a host for a bloodmeal, plants for a source of energy and suitable sites for oviposition. Here, we examined a cluster of eight odorant receptors (ORs), which includes one OR, CquiOR1
Leah Armon et al.
Fertility and sterility, 102(3), 885-890 (2014-07-27)
To characterize the nature of the human oocyte-derived chemoattractant. Laboratory in vitro study. Academic research institute. Ten healthy sperm donors. Oocyte-conditioned media from women undergoing IVF treatment because of male factor infertility. Sperm samples were processed by the migration-sedimentation technique. Oocyte-conditioned
Eunice A Owino et al.
Parasites & vectors, 8, 253-253 (2015-05-01)
Effective surveillance and estimation of the biting fraction of Aedes aegypti is critical for accurate determination of the extent of virus transmission during outbreaks and inter-epidemic periods of dengue and chikungunya fever. Here, we describe the development and use of
Ádám Tölgyesi et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 32(9), 1512-1522 (2015-07-28)
Alternaria toxins and citrinin are mycotoxins produced by fungi growing on different raw materials and agricultural commodities. Maximum levels of these toxins in foods are currently under consideration by the European Commission as a risk management measure. In this study
实验方案
-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene
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