410829
1,2-Epoxy-9-decene
96%
Synonym(s):
(7-Octenyl)oxirane
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About This Item
Recommended Products
Quality Level
Assay
96%
form
liquid
refractive index
n20/D 1.442 (lit.)
density
0.842 g/mL at 25 °C (lit.)
SMILES string
C=CCCCCCCC1CO1
InChI
1S/C10H18O/c1-2-3-4-5-6-7-8-10-9-11-10/h2,10H,1,3-9H2
InChI key
FCZHJHKCOZGQJZ-UHFFFAOYSA-N
Related Categories
General description
1,2-Epoxy-9-decene is an unsaturated epoxide. Hydrogenation of the C=C bond of 1,2-epoxy-9-decene over palladium nanoparticles, namely PdOAc,N has been reported.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
172.4 °F - closed cup
Flash Point(C)
78 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Langmuir : the ACS journal of surfaces and colloids, 24(24), 13957-13961 (2009-04-11)
A versatile two-step method has been developed that allows linking of biomolecules covalently to hydrogen-terminated group-IV semiconductors by means of epoxy-alkenes. First, the terminal C==C double bond of the alkene forms a covalent bond with the silicon, germanium, or diamond
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Structurally diverse secondary amine-functionalized poly(propylene imine) (PPI) dendrimers capable of tunable nitric oxide (NO) release were synthesized in a straightforward, one-step manner using ring-opening or conjugate-addition reactions with propylene oxide (PO), styrene oxide (SO), acrylonitrile (ACN), poly(ethylene glycol) methyl ether
Reactivity versus Stability of Oxiranes under Palladium-Catalyzed Reductive Conditions.
European Journal of Organic Chemistry, 2009(7), 961-985 (2009)
Biomacromolecules, 14(10), 3589-3598 (2013-08-22)
A series of amphiphilic nitric oxide (NO)-releasing poly(amidoamine) (PAMAM) dendrimers with different exterior functionalities were synthesized by a ring-opening reaction between primary amines on the dendrimer and propylene oxide (PO), 1,2-epoxy-9-decene (ED), or a ratio of the two, followed by
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