Site Navigation
Categories:
Oxygen heterocycles
Ethers
IARC Group 2B carcinogens
Ether solvents

Summary Of: 1,4-Dioxane

1,4-Dioxane has a weak... 1,4-Dioxane is classified as an... 1,4-Dioxane is primarily used in solvent applications for the manufacturing sector... 1,4-Dioxane is a known eye and respiratory tract irritant... Accidental worker exposure to 1,4-dioxane has resulted in several deaths... listed 1,4-dioxane as a chemical known to cause cancer on January 1... 1,4-Dioxane is highly soluble in groundwater... a 1,4-dioxane plume is often much larger... testing sponsored by an independent consumers organization found 1,4-dioxane in almost half of tested personal... Occurrence of 1,4-Dioxane in Cosmetic Raw Materials and Finished Cosmetic Products... Press conference on 1,4-dioxane found in children... Press conference on 1,4-dioxane found in personal care products labeled...

Encyclodia Page On: 1,4-Dioxane

These Are Links To Other Documents
Dioxin (chemical) | Chemical structure of dioxane | 1,4-dioxane | IUPAC name | CAS number | EINECS number | SMILES | Molecular formula | Molar mass | Density | Melting point | Boiling point | Std enthalpy of
formation
| Std enthalpy of
combustion
| Standard molar
entropy
| EU classification | Carc. Cat. 3 | R-phrases | R11 | R19 | R36/37 | R40 | R66 | S-phrases | (S2) | S9 | S16 | S36/37 | S46 | Flash point | standard state
(at 25 °C, 100 kPa)
| Infobox references | heterocyclic | organic compound | liquid | temperature | pressure | molecular formula | aprotic solvent | smell | diethyl ether | isomeric | peroxide | tetrahydrofuran | ether | oxygen | atoms | functional group | polar | diethyl ether | carbons | miscible | water | hygroscopic | molecular mass | boiling point | Grignard | Schlenk equilibrium | dioxin | | foaming agent | NMR | tetramethylsilane | D2O | peroxides | Distillation | IARC | Group 2B carcinogen | proposition 65 | groundwater | Ether | Crown ether | Categories | Oxygen heterocycles | Ethers | IARC Group 2B carcinogens | Ether solvents |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "1,4-Dioxane".