1,2-Epoxyoctane
Product Information
Molecular Formula
C8H16O
Molecular Weight
128.21
Description
Applications: 1,2-Epoxyoctane is a useful research chemical.
Synonyms
2-hexyloxirane
IUPAC Name
2-hexyloxirane
SMILES
CCCCCCC1CO1
InChI
InChI=1S/C8H16O/c1-2-3-4-5-6-8-7-9-8/h8H,2-7H2,1H3
InChI Key
NJWSNNWLBMSXQR-UHFFFAOYSA-N
Boiling Point
167 °C
Flash Point
37 °C
Density
0.835 g/mL at 20 °C (lit.)
Appearance
Colorless to almost colorless clear liquid
Storage
2-8 °C
Refractive Index
n20/D 1.42 (lit.)
LogP
2.35560
Safety Information
Hazards
H226:
Flammable liquid and vapour.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Flammable liquid and vapour.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, and P501
Signal Word
Warning
Computed Properties
XLogP3
3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
5
Exact Mass
128.120115130 g/mol
Monoisotopic Mass
128.120115130 g/mol
Topological Polar Surface Area
12.5Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
71
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114057992-A | Resin composition for carbon fiber molding | 2021-11-02 |
| CN-113956441-A | Die pressing free radical modified epoxy resin composition | 2021-10-29 |
| CN-113912843-A | Porous metalloporphyrin polymer containing benzimidazole ionic liquid and preparation method and application thereof | 2021-10-19 |
| CN-113813939-A | Application of COF material based on C = C bond connection in preparation of chiral chromatography stationary phase | 2021-10-14 |
| CN-113845126-A | Titanium-silicon molecular sieve and preparation method and application thereof | 2021-05-31 |
| CN-113248968-A | Environment-friendly anti-skinning and viscosity-removing agent and preparation method thereof | 2021-05-26 |
| CN-112920583-A | Poly-L-lactic acid foaming material with rapid crystallization capacity and preparation method thereof | 2021-04-14 |
| CN-113150221-A | Unsaturated polyester and free radical modified epoxy resin composition | 2021-04-09 |
| CN-113150496-A | Epoxy resin reinforced material | 2021-04-09 |
| CN-113004507-A | Rapidly-crystallized poly-L-lactic acid and preparation method thereof, and polylactic acid foam material and preparation method thereof | 2021-03-08 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 21515382 | 2011-09-01 | Cloning and characterization of an epoxide hydrolase from Cupriavidus metallidurans-CH34 | Protein expression and purification |
| 20204614 | 2010-06-01 | Searching for monooxygenases and hydrolases in bacteria from an extreme environment | Applied microbiology and biotechnology |
| 19113936 | 2009-02-06 | Alkylation of 2-substituted (6-methyl-2-pyridyl)methyllithium species with epoxides | The Journal of organic chemistry |
| 16377903 | 2005-12-01 | Isolation and functional analysis of cytochrome P450 CYP153A genes from various environments | Bioscience, biotechnology, and biochemistry |
| 16200537 | 2005-11-01 | Improved catalytic activity of homochiral dimeric cobalt-salen complex in hydrolytic kinetic resolution of terminal racemic epoxides | Chirality |
| 14626425 | 2003-10-01 | Calcium alginate entrapment of the yeast Rhodosporidium toruloides for the kinetic resolution of 1,2-epoxyoctane | Biotechnology letters |
| 11346811 | 2001-05-10 | Spontaneous intracerebral hemorrhage | The New England journal of medicine |
| 1322 | 1976-01-01 | Comparison of amino acids bathing the oxyntic gland area in the stimulation of gastric secretion | Gastroenterology |
