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1,4-Dioxane
[CAS# 123-91-1]

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Complete supplier list of 1,4-Dioxane
Identification
Classification Biochemical >> Enzymes and coenzymes
Name 1,4-Dioxane
Synonyms Diox; Diethylene dioxide
Molecular Structure CAS # 123-91-1, 1,4-Dioxane, Diox, Diethylene dioxide
Molecular Formula C4H8O2
Molecular Weight 88.11
CAS Registry Number 123-91-1
EC Number 204-661-8
SMILES C1COCCO1
Properties
Density 1.033
Melting point 12 ºC
Boiling point 101 ºC
Refractive index 1.4205-1.422
Flash point 12 ºC
Water solubility SOLUBLE
Safety Data
Hazard Symbols symbol symbol symbol   GHS02;GHS08;GHS07 Danger    Details
Hazard Statements H225-H350-H335-H319    Details
Precautionary Statements P203-P210-P233-P240-P241-P242-P243-P261-P264+P265-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P318-P319-P337+P317-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.2H225
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
CarcinogenicityCarc.2H351
CarcinogenicityCarc.1BH350
Specific target organ toxicity - single exposureSTOT SE3H336
CarcinogenicityCarc.1BH350i
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE1H370
Eye irritationEye Irrit.2AH319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - repeated exposureSTOT RE2H373
Specific target organ toxicity - repeated exposureSTOT RE1H372
CarcinogenicityCarc.2H350
Transport Information UN 1165
SDS Available
up Discovory and Applicatios
1,4-Dioxane is a cyclic organic compound characterized by a six-membered ring containing two oxygen atoms and four carbon atoms. The compound has a molecular formula of C4H8O2 and is commonly represented as a colorless, flammable liquid with a distinctive odor. 1,4-Dioxane was first synthesized in the early 1900s, with its discovery attributed to the work of chemists seeking to develop new solvents and reaction media. Over the years, its unique chemical properties have led to various applications in both industrial and laboratory settings.

One of the primary applications of 1,4-dioxane is as a solvent. Its ability to dissolve a wide range of organic and inorganic compounds makes it invaluable in many chemical processes. In laboratories, 1,4-dioxane is often used as a reaction medium in organic synthesis, particularly in reactions involving nucleophilic substitution and polymerization. Its relatively low boiling point and high polarity also contribute to its utility as a solvent for extracting and purifying compounds in various chemical reactions.

In addition to its role as a solvent, 1,4-dioxane is utilized in the production of other chemicals. It serves as a key intermediate in the synthesis of various polymers, surfactants, and agrochemicals. For instance, 1,4-dioxane is involved in the manufacture of polyethylene glycol (PEG), a widely used polymer in pharmaceuticals, cosmetics, and food processing. The compound's unique properties allow for the creation of materials with tailored characteristics, making it a valuable building block in material science.

Another significant application of 1,4-dioxane is in the field of pharmaceuticals. It is used in the formulation of certain drug products and as a stabilizer in the preparation of pharmaceutical intermediates. Its ability to enhance the solubility and bioavailability of active pharmaceutical ingredients (APIs) has made it an essential component in drug development processes. Moreover, 1,4-dioxane's low toxicity profile compared to other solvents has contributed to its acceptance in the pharmaceutical industry.

Despite its usefulness, the environmental and health implications of 1,4-dioxane have raised concerns. The compound has been classified as a potential human carcinogen, and its presence in groundwater and surface water poses a risk to aquatic life and human health. As a result, regulatory agencies have established guidelines to limit its use and emissions. Researchers are actively investigating alternative solvents and processes to reduce reliance on 1,4-dioxane while maintaining the efficiency and effectiveness of chemical reactions.

In conclusion, 1,4-dioxane is a versatile compound with significant applications in various industries, including solvents, chemical synthesis, and pharmaceuticals. Its discovery over a century ago has paved the way for numerous advancements in chemical processes and material development. However, ongoing research and regulatory scrutiny highlight the importance of balancing its utility with environmental and health considerations.
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