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dioxane
Sign in to saveAlso known as Diethylene dioxide, Diethylene ether, Dioxan, p-Dioxane, dioxane-1,4, 1,4-dioxacyclohexane, glycol ethylene ether, di(ethylene oxide)
1,4-Dioxane () is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers (1,2- and 1,3-) are rarely encountered.
Chemical data
- Formula
- C4H8O2
- Molecular weight
- 88.11 g/mol
- IUPAC name
- 1,4-dioxane
- SMILES
- C1COCCO1
- InChIKey
- RYHBNJHYFVUHQT-UHFFFAOYSA-N
- XLogP
- -0.3
- Polar surface area
- 18.5 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Mass
- 88.052
Show 20 more facts
- flash point
- 55
- chemical formula
- C₄H₈O₂
- lower flammable limit
- 2
- NIOSH Pocket Guide ID
- 0237
- density
- 1.03
- immediately dangerous to life or health
- 1800
- melting point
- 11.8
- boiling point
- 101.5
- vapor pressure
- 29
- upper flammable limit
- 22
- ionization energy
- 9.19
- time-weighted average exposure limit
- 360
- ceiling exposure limit
- 3.6
- canonical SMILES
- C1COCCO1
- subject has role
- carcinogen
- standard enthalpy of formation
- -354
- refractive index
- 1.42241
- Commons category
- 1,4-Dioxane
- electric dipole moment
- 0
- found in taxon
- Opuntia ficus-indica
via Wikidata · CC0
~8 min read
Encyclopedic overview
12 sectionsContents
- History and synthesis
- Structure
- Uses
- Trichloroethane transport
- As a solvent
- Toxicology
- Safety
- Explosion hazard
- Environment
- Consumer products
- See also
- References
1,4-Dioxane () is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers (1,2- and 1,3-) are rarely encountered.
1,4-Dioxane is miscible in water, essentially nonvolatile when dissolved in water, not well adsorbed by activated carbon, and not readily oxidized by common oxidants.
Excerpted from Wikipedia’s “dioxane” article, available under the CC BY-SA 4.0 licence.