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线性分子式:
CH3(CH2)3CH=CH(CH2)9CHO
化学文摘社编号:
分子量:
238.41
EC Number:
258-876-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1867354
MDL number:
grade
purum
assay
≥95.0% (GC)
refractive index
n20/D 1.455
density
0.963 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
[H]C(=O)CCCCCCCCC\C=C/CCCC
InChI
1S/C16H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h5-6,16H,2-4,7-15H2,1H3/b6-5-
InChI key
AMTITFMUKRZZEE-WAYWQWQTSA-N
Application
许多物种的信息素
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
141.8 °F - closed cup
flash_point_c
61 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Hong-Lei Wang et al.
Insect biochemistry and molecular biology, 35(6), 575-583 (2005-04-29)
Two Helicoverpa species, H. armigera and H. assulta use (Z)-11-hexadecenal and (Z)-9-hexadecenal as their sex attractant pheromone components but in opposite ratios. Since both female and male interspecific hybrids produced by female H. assulta and male H. armigera have been
Ewald Grosse-Wilde et al.
The European journal of neuroscience, 25(8), 2364-2373 (2007-04-21)
Males of the moth species Heliothis virescens are able to detect the female-released pheromone with remarkable sensitivity and specificity, distinguishing between highly related pheromonal compounds. In the past, electrophysiological studies succeeded in assigning sensory hairs to identified compounds revealing three
Basal cytotoxicity of four insect sex pheromones in CHO-K1 cells.
A E Bayoumi et al.
Bulletin of environmental contamination and toxicology, 68(2), 302-308 (2002-01-30)

