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Ethylenedioxydimethanol is used for the preservation of pigment slurries, filler suspensions, polymer dispersions, solutions and dispersions of glues and thickeners, concrete additives, detergents, oil emulsions, polishes, and other chemical-technical water-based preparations.
Ethylenedioxydimethanol can be used to combat bacteria, mold, and yeast.
Ethylenedioxydimethanol is bactericide; used in method for preparing reactive yellow dye ink for digital printing.
CAS: 3586-55-8
MF: C4H10O4
MW: 122.12
EINECS: 222-720-6
Ethylenedioxydimethanol, also known as EDDM, is an organic compound that is used in a variety of scientific applications.
Ethylenedioxydimethanol is a versatile molecule that is often used in laboratory experiments due to its unique properties.
This paper will provide an overview of Ethylenedioxydimethanol’s synthesis methods, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions.
Ethylenedioxydimethanol has several advantages for use in laboratory experiments.
Ethylenedioxydimethanol is a relatively inexpensive reagent, and it is relatively easy to synthesize.
Ethylenedioxydimethanol is also a very versatile molecule, and can be used in a variety of applications.
The main limitation of Ethylenedioxydimethanol is that it is not very stable, and can degrade over time.
Ethylenedioxydimethanol has a variety of potential future applications.
Ethylenedioxydimethanol could be used in the synthesis of more complex organic compounds, or in the development of new pharmaceuticals.
Ethylenedioxydimethanol could also be used to develop new techniques for separating and analyzing molecules, or to create new polymers.
Additionally, Ethylenedioxydimethanol could be used to study the mechanism of action of other molecules, or to develop new catalysts for chemical reactions.
Ethylenedioxydimethanol is a slow-release bactericide and desulfurizer with low
toxicity, high efficiency and gas-phase sterilization ability.
Ethylenedioxydimethanol is suitable for inhibiting the growth and reproduction of microorganismsin various humid environments, preventing corruption and odor, ensuring the safe operation of the system, and is also widely used in the removal of hydrogen sulfide from.
Ethylenedioxydimethanol is a product developed for water-based system with excellent compatibility.
Ethylenedioxydimethanol is suitable for totalsynthesis,semisynthesis and some emulsified metal working fluids.
Ethylenedioxydimethanol has good bactericidal effect in the range of pH 6-11, and its pH value is neutral, does not contain alcohol amine;
Ethylenedioxydimethanol is a slow-release bactericide to prevent corruption and odor and ensure the safe operation of the system.
Ethylenedioxydimethanol has almost no corrosion to steel.
In the environment of multiple media, Ethylenedioxydimethanol has good selectivity for H2S and high sulfur removal efficiency.
Ethylenedioxydimethanol does not contain salt and is not easy to cause salt precipitation;
The filling processis simple.
The dosing is mainly through the metering pump, and the energy consumption is very small.
Desulfurization reaction of desulfurizer can occur at room temperature.
The process of eliminating hydrogen sulfide is an exothermic process, and generally does not need to consume energy.
Ethylenedioxydimethanol is not easy to cause salt deposition and corrosion;
Ethylenedioxydimethanol does not affect the activity of the catalyst.
Ethylenedioxydimethanol should be stored in a dry and cool place.
Ethylenedioxydimethanol can be stored stably for 2 years at room temperature.
Ethylenedioxydimethanol Physico-chemical Properties
Molecular Formula: C4H10O4
Molar Mass: 122.12
Density: 1.193
Boling Point: 90℃
Flash Point: 8℃
pKa: 12.76±0.10(Predicted)
Synthesis Method
Ethylenedioxydimethanol can be synthesized in a few different ways.
The most common method is by the reaction of ethylene glycol and dimethyl sulfoxide (DMSO).
This reaction is catalyzed by a strong acid, such as sulfuric acid, and produces Ethylenedioxydimethanol and water as byproducts.
Another method of synthesis is the reaction of ethylene glycol and dimethylformamide (DMF).
This reaction is also catalyzed by sulfuric acid, and produces Ethylenedioxydimethanol, water, and dimethylformamide as byproducts.
Uses
Ethylenedioxydimethanol is a versatile molecule that has a variety of scientific applications.
Ethylenedioxydimethanol is used in biochemistry and molecular biology as a reagent for the synthesis of DNA and proteins.
Ethylenedioxydimethanol is also used as a solvent in chromatography, a technique used to separate and analyze molecules.
Ethylenedioxydimethanol has also been used in the production of polymers, in the synthesis of organic compounds, and in the preparation of pharmaceuticals.
Mechanism of Action
Ethylenedioxydimethanol acts as a catalyst for a variety of chemical reactions.
Ethylenedioxydimethanol is able to form hydrogen bonds with other molecules, allowing it to act as a bridge between two reacting molecules.
Ethylenedioxydimethanol is also able to form non-covalent bonds with other molecules, which helps to stabilize the reaction.
Biochemical and Physiological Effects
Ethylenedioxydimethanol is an organic compound that is generally considered to be non-toxic and non-carcinogenic.
Ethylenedioxydimethanol is not known to have any significant biochemical or physiological effects on humans or animals.
Synonyms
(Ethylenedioxy)dimethanol
3586-55-8
Dimethylol glycol
Ethylene glycol bis(semiformal)
2-(hydroxymethoxy)ethoxymethanol
1,2-Bis(hydroxymethoxy)ethane
1,2-Bis[hydroxymethoxy]ethane
1,6-dihydroxy-2,5-dioxahexane
Y772Z5O19G
dimethanol
UNII-Y772Z5O19G
1,6-dihydroxy-2,5-dioxyhexane
EINECS 222-720-6
(1,2-Ethanediylbis(oxy))bismethanol
Methanol, (1,2-ethanediylbis(oxy))bis-
GROTAN TK5
SCHEMBL561721
DIMETHYLOL GLYCOL [INCI]
DTXSID5041225
[2-(hydroxymethoxy)ethoxy]methanol
(1,2-ETHANEDIYLBIS(OXY)BISMETHANOL
W-109911
Q27294333
METHANOL, 1,1'-(1,2-ETHANEDIYLBIS(OXY))BIS-
(ethylenedioxy)dimethanol
2-methyloloxyethoxymethanol
ethyleneglycoldimethanolether
1,6-Dihydroxy-2,5-dioxyhexane
ethylene glycol dimethanol ether
2-(hydroxymethoxy)ethoxymethanol
1,2-ETHANDIYLBIS(OXY)BISMETHANOL
Methanol,1,2-ethanediylbis(oxy)bis-
[1,2-ethanediylbis(oxy)]bis-Methanol
Methanol, 1,2-ethanediylbis(oxy)bis-
