Octanoic acid, octylester structure
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Common Name | Octanoic acid, octylester | ||
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CAS Number | 2306-88-9 | Molecular Weight | 256.42400 | |
Density | 0.859 g/mL at 25ºC(lit.) | Boiling Point | 307ºC(lit.) | |
Molecular Formula | C16H32O2 | Melting Point | -18ºC(lit.) | |
MSDS | Chinese USA | Flash Point | >230 °F |
Name | octyl octanoate |
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Synonym | More Synonyms |
Density | 0.859 g/mL at 25ºC(lit.) |
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Boiling Point | 307ºC(lit.) |
Melting Point | -18ºC(lit.) |
Molecular Formula | C16H32O2 |
Molecular Weight | 256.42400 |
Flash Point | >230 °F |
Exact Mass | 256.24000 |
PSA | 26.30000 |
LogP | 5.25060 |
Vapour Pressure | 0.000817mmHg at 25°C |
Index of Refraction | 1.439 |
Personal Protective Equipment | Eyeshields;Gloves |
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RIDADR | NONH for all modes of transport |
Precursor 10 | |
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DownStream 2 | |
The influence of surface charge and photo-reactivity on skin-permeation enhancer property of nano-TiO₂ in ex vivo pig skin model under indoor light.
Int. J. Pharm. 467(1-2) , 90-9, (2014) Several topical products contain nanometric TiO2 (nano-TiO2), which is a useful and safe component that absorbs UV light and does not cross skin barrier. However, nano-TiO2 may impregnate the first la... |
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Spitting out information: Trigona bees deposit saliva to signal resource locations.
Proc. Biol. Sci. 274(1611) , 895-8, (2007) Stingless bees of the species Trigona spinipes (Fabricius 1793) use their saliva to lay scent trails communicating the location of profitable food sources. Extracts of the cephalic labial glands of th... |
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Phytochemical analysis and allelopathic activity of essential oils of Ecballium elaterium A. Richard growing in Iran.
Nat. Prod. Res. 24(18) , 1704-9, (2010) The hydrodistillated essential oils from leaves and fruits of Ecballium elaterium were analysed by GC-MS. Octyl octanoate (30.0%), 3-(6,6- dimethyl-5-oxohept-2-enyl)-cyclohexanone (20.4%) and hexahydr... |
n-Octyl caprylate |
UNII-MM00XO86JQ |
n-octyl n-octanoate |
Octyl caprylate |
1-octyl octanate |
Octanoic acid,octylester |
n-octanoic acid octyl ester |
Octyl octylate |