1,4-Dioxane
From Wikipedia, the free encyclopedia
| 1,4-Dioxane | |
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| Chemical name | 1,4-Dioxane 1,4-Dioxacyclohexane |
| Other names | [1,4]Dioxane p-Dioxane |
| Chemical formula | C4H8O2 |
| Molecular mass | 88.11 g/mol |
| Melting point | 11.8°C |
| Boiling point | 101.1°C |
| Density | 1.033 g/cm³ |
| CAS number | [123-91-1] |
| EINECS number | 204-661-8 |
| SMILES | C1OCCOC1 |
| Thermodynamic data | |
| Standard enthalpy of formation ΔfH°liquid |
-354 kJ/mol |
| Standard enthalpy of combustion ΔcH°liquid |
-2363 kJ/mol |
| Standard molar entropy S°liquid |
196.6 J.K–1.mol–1 |
| Safety data | |
| EU classification | Flammable (F) Carc. Cat. 3 Irritant (Xn) |
| R-phrases | R11, R19, R36/37, R40, R66 |
| S-phrases | S2, S9, S16, S36/37, S46 |
| Flash Point | 12 °C |
| Disclaimer and references | |
1,4-Dioxane, often just called dioxane, is a clear, colorless heterocyclic organic compound which is a liquid at room temperature and pressure. It has the molecular formula C4H8O2 and a boiling point of 101 °C. It is commonly used as an aprotic solvent. 1,4-Dioxane has a weak smell similar to that of diethyl ether. There are also two other less common isomeric compounds, 1,2-dioxane and 1,3-dioxane. 1,2-Dioxane is a peroxide which forms naturally in old bottles of tetrahydrofuran.
1,4-Dioxane is classified as an ether, with each of its two oxygen atoms forming an ether functional group. It is more polar than diethyl ether, which also has four carbons, but only one ether functional group. Diethyl ether is rather insoluble in water, but 1,4-dioxane is miscible with water and is hygroscopic. Its higher polarity and slightly higher molecular mass also gives it a substantially higher boiling point than diethyl ether. When used as a solvent for a grignard reaction, Dioxane favorably affects the formation of magnesium halide salts in the Schlenk equilibrium.
The name dioxane should not be confused with dioxin, which is a different compound but is also a diether (two ether functional groups).
Small blue numbers show numbering of atoms in rings.
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[edit] Uses
1,4-Dioxane is primarily used in solvent applications for the manufacturing sector; however, it is also found in fumigants and automotive coolant. Additionally, the chemical is also used as a foaming agents and appears as an accidental byproduct of the ethoxylation[1] process in cosmetics manufacturing. It may contaminate cosmetics and personal care products such as deodorants, shampoos, toothpastes and mouthwashes.[2]
[edit] Safety concerns
Like many other ethers, dioxanes combine with atmospheric oxygen on standing to form explosive peroxides, similar to many other ethers. Distillation of dioxanes concentrates these peroxides increasing the danger. Appropriate precautions should be taken.
1,4-dioxane is a known eye and respiratory tract irritant. It is suspected of causing damage to the central nervous system, liver and kidneys.[3] Accidental worker exposure to 1,4-dioxane has resulted in several deaths.[4] Dioxane is classified by the IARC as a Group 2B carcinogen: possibly carcinogenic to humans due to the fact that it is a known carcinogen in animals.[5]
[edit] See also
[edit] References
- ^ Roderick E. Black. Occurrence of 1,4-Dioxane in Cosmetic Raw Materials and Finished Cosmetic Products. Journal of IAOC International. Retrieved on 2006-02-02.
- ^ CHEC Chemical Summary: 1,4-dioxane. Children's Health Environmental Coalition. Retrieved on 2006-02-02.
- ^ International Chemical Safety Card. National Institute for Occupational Safety and Health. Retrieved on 2006-02-02.
- ^ OPPT Chemical Fact Sheets 1,4-Dioxane (CAS No. 123-91-1). United States Environmental Protection Agency. Retrieved on 2006-02-02.
- ^ Eleventh Report on Carcinogens. United States Department of Health and Human Services’ National Toxicology Program. Retrieved on 2006-02-02.
