1,4-Dioxane

1,4-Dioxane

Names
Preferred IUPAC name 1,4-Dioxane
Systematic IUPAC name 1,4-Dioxacyclohexane
Other names [1,4]Dioxane p-Dioxane [6]-crown-2 Diethylene dioxide Diethylene ether Dioxane solvent
Identifiers
CAS Number	123-91-1 Y
3D model (JSmol)	Interactive image
Beilstein Reference	102551
ChEBI	CHEBI:47032 Y
ChEMBL	ChEMBL453716 Y
ChemSpider	29015 Y
DrugBank	DB03316 Y
ECHA InfoCard	100.004.239
EC Number	204-661-8
KEGG	C14440 Y
PubChem CID	31275
RTECS number	JG8225000
UNII	J8A3S10O7S Y
UN number	1165
CompTox Dashboard (EPA)	DTXSID4020533
InChI InChI=1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2 Y Key: RYHBNJHYFVUHQT-UHFFFAOYSA-N Y InChI=1/C4H8O2/c1-2-6-4-3-5-1/h1-4H2 Key: RYHBNJHYFVUHQT-UHFFFAOYAN
SMILES O1CCOCC1
Properties
Chemical formula	C4H8O2
Molar mass	88.106 g·mol−1
Appearance	Colorless liquid[1]
Odor	Mild, diethyl ether-like[1]
Density	1.033 g/mL
Melting point	11.8 °C (53.2 °F; 284.9 K)
Boiling point	101.1 °C (214.0 °F; 374.2 K)
Solubility in water	Miscible
Vapor pressure	29 mmHg (20 °C)[1]
Magnetic susceptibility (χ)	−52.16·10−6 cm3/mol
Thermochemistry
Std molar entropy (S⦵298)	196.6 J/K·mol
Std enthalpy of formation (ΔfH⦵298)	−354 kJ/mol
Std enthalpy of combustion (ΔcH⦵298)	−2363 kJ/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards	Suspected human carcinogen[1]
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H302, H305, H315, H319, H332, H336, H351, H370, H372, H373
Precautionary statements	P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P281, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P307+P311, P308+P313, P312, P314, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)	2 3 1
Flash point	12 °C (54 °F; 285 K)
Autoignition temperature	180 °C (356 °F; 453 K)
Explosive limits	2.0–22%[1]
Lethal dose or concentration (LD, LC):
LD50 (median dose)	5 g/kg (mouse, oral) 4 g/kg (rat, oral) 3 g/kg (guinea pig, oral) 7.6 g/kg (rabbit, dermal)
LC50 (median concentration)	10,109 ppm (mouse, 2 hr) 12,568 ppm (rat, 2 hr)[2]
LCLo (lowest published)	1000–3000 ppm (guinea pig, 3 hr) 12,022 ppm (cat, 7 hr) 2085 ppm (mouse, 8 hr)[2]
NIOSH (US health exposure limits):
PEL (Permissible)	TWA 100 ppm (360 mg/m3) [skin][1]
REL (Recommended)	Ca C 1 ppm (3.6 mg/m3) [30-minute][1]
IDLH (Immediate danger)	Ca [500 ppm][1]
Related compounds
Related compounds	Oxane Trioxane Tetroxane Pentoxane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

1,4-Dioxane (/daɪˈɒkseɪn/) 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.

Dioxane is used as a solvent for a variety of practical applications as well as in the laboratory, and also as a stabilizer for the transport of chlorinated hydrocarbons in aluminium containers.^[3]

Dioxane is produced by the acid-catalysed dehydration of diethylene glycol, which in turn is obtained from the hydrolysis of ethylene oxide.

In 1985, the global production capacity for dioxane was between 11,000 and 14,000 tons.^[4] In 1990, the total U.S. production volume of dioxane was between 5,250 and 9,150 tons.^[5]

The dioxane molecule is centrosymmetric, meaning that it adopts a chair conformation, typical of relatives of cyclohexane. However, the molecule is conformationally flexible, and the boat conformation is easily adopted, e.g. in the chelation of metal cations. Dioxane resembles a smaller crown ether with only two ethyleneoxyl units.

In the 1980s, most of the dioxane produced was used as a stabilizer for 1,1,1-trichloroethane for storage and transport in aluminium containers. Normally aluminium is protected by a passivating oxide layer, but when these layers are disturbed, the metallic aluminium reacts with trichloroethane to give aluminium trichloride, which in turn catalyses the dehydrohalogenation of the remaining trichloroethane to vinylidene chloride and hydrogen chloride. Dioxane "poisons" this catalysis reaction by forming an adduct with aluminium trichloride.^[4]

Dioxane is used in a variety of applications as a versatile aprotic solvent, e.g. for inks, adhesives, and cellulose esters. It is substituted for tetrahydrofuran (THF) in some processes, because of its lower toxicity and higher boiling point (101 °C, versus 66 °C for THF).^[6]

While diethyl ether is rather insoluble in water, dioxane is miscible and in fact is hygroscopic. At standard pressure, the mixture of water and dioxane in the ratio 17.9:82.1 by mass is a positive azeotrope that boils at 87.6 °C.^[7]

The oxygen atoms are weakly Lewis-basic. It forms adducts with a variety of Lewis acids. It is classified as a hard base and its base parameters in the ECW model are E_B = 1.86 and C_B = 1.29.

Dioxane produces coordination polymers by linking metal centers.^[8] In this way, it is used to drive the Schlenk equilibrium, allowing the synthesis of dialkyl magnesium compounds.^[4] Dimethylmagnesium is prepared in this manner:^[9][10]

2 CH₃MgBr + (C₂H₄O)₂ → MgBr₂(C₂H₄O)₂ + (CH₃)₂Mg

Dioxane is used as an internal standard for nuclear magnetic resonance spectroscopy in deuterium oxide.^[11]

Dioxane has an LD₅₀ of 5170 mg/kg in rats.^[4] It is irritating to the eyes and respiratory tract. Exposure may cause damage to the central nervous system, liver and kidneys.^[12] In a 1978 mortality study conducted on workers exposed to 1,4-dioxane, the observed number of deaths from cancer was not significantly different from the expected number.^[13] Dioxane is classified by the National Toxicology Program as "reasonably anticipated to be a human carcinogen".^[14] It is also classified by the IARC as a Group 2B carcinogen: possibly carcinogenic to humans because it is a known carcinogen in other animals.^[15] The United States Environmental Protection Agency classifies dioxane as a probable human carcinogen (having observed an increased incidence of cancer in controlled animal studies, but not in epidemiological studies of workers using the compound), and a known irritant (with a no-observed-adverse-effects level of 400 milligrams per cubic meter) at concentrations significantly higher than those found in commercial products.^[16] Animal studies in rats suggest that the greatest health risk is associated with inhalation of vapors in the pure form.^[17][18][19] The State of New York has adopted a first-in-the-nation drinking water standard for 1,4-Dioxane and set the maximum contaminant level of 1 part per billion.^[20]

Like some other ethers, dioxane combines with atmospheric oxygen upon prolonged exposure to air to form potentially explosive peroxides. Distillation of these mixtures is dangerous. Storage over metallic sodium could limit the risk of peroxide accumulation.

Dioxane tends to concentrate in the water and has little affinity for soil. It is resistant to abiotic degradation in the environment, and was formerly thought to also resist biodegradation. However, more recent studies since the 2000s have found that it can be biodegraded through a number of pathways, suggesting that bioremediation can be used to treat 1,4-dioxane contaminated water.^[21][22]

Dioxane has affected groundwater supplies in several areas. Dioxane at the level of 1 μg/L (~1 ppb) has been detected in many locations in the US.^[5] In the U.S. state of New Hampshire, it had been found at 67 sites in 2010, ranging in concentration from 2 ppb to over 11,000 ppb. Thirty of these sites are solid waste landfills, most of which have been closed for years. In 2019, the Southern Environmental Law Center successfully sued Greensboro, North Carolina's Wastewater treatment after 1,4-Dioxane was found at 20 times above EPA safe levels in the Haw River.^[23]

As a byproduct of the ethoxylation process, a route to some ingredients found in cleansing and moisturizing products, dioxane can contaminate cosmetics and personal care products such as deodorants, perfumes, shampoos, toothpastes and mouthwashes.^[24][25] The ethoxylation process makes the cleansing agents, such as sodium laureth sulfate and ammonium laureth sulfate, less abrasive and offers enhanced foaming characteristics. 1,4-Dioxane is found in small amounts in some cosmetics, a yet unregulated substance used in cosmetics in both China and the U.S.^[26] Research has found the chemical in ethoxylated raw ingredients and in off-the-shelf cosmetic products. The Environmental Working Group (EWG) found that 97% of hair relaxers, 57% of baby soaps and 22 percent of all products in Skin Deep, their database for cosmetic products, are contaminated with 1,4-dioxane.^[27]

Since 1979 the U.S. Food and Drug Administration (FDA) have conducted tests on cosmetic raw materials and finished products for the levels of 1,4-dioxane.^[28] 1,4-Dioxane was present in ethoxylated raw ingredients at levels up to 1410 ppm (~0.14%wt), and at levels up to 279 ppm (~0.03%wt) in off the shelf cosmetic products.^[28] Levels of 1,4-dioxane exceeding 85 ppm (~0.01%wt) in children's shampoos indicate that close monitoring of raw materials and finished products is warranted.^[28] While the FDA encourages manufacturers to remove 1,4-dioxane, it is not required by federal law.^[29]

On 9 December 2019, New York passed a bill to ban the sale of cosmetics with more than 10 ppm of 1,4-dioxane as of the end of 2022. The law will also prevent the sale of household cleaning and personal care products containing more than 2 ppm of 1,4-dioxane at the end of 2022.^[30]

• Dioxolane
• 9-crown-3
• Dioxane tetraketone
• Oxalic anhydride
• Dioxanone