Ethylene Glycol Dicarboxylate

Ethylene Glycol Dicarboxylate

Poly(ethylene glycol) dicarboxylate (PEGDC) contains carboxyl groups that increase the adhesive strength of the film to the tissue. [17,18] A lower molecular weight of PEGDC might improve the mechanical strength and physical properties of hydrogel film due to the higher physical cross-link density.

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Product Introduction

What is Ethylene Glycol Dicarboxylate

 

 

Poly(ethylene glycol) dicarboxylate (PEGDC) contains carboxyl groups that increase the adhesive strength of the film to the tissue. [17,18] A lower molecular weight of PEGDC might improve the mechanical strength and physical properties of hydrogel film due to the higher physical cross-link density.

 

 

 
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Storage Conditions of Ethylene Glycol Diacetate

Ethylene glycol diacetate should avoid contact with alkali, acid, oxidizing agent and reducing agent during storage. The compound is a flammable liquid and is non-corrosive to metals. It can be stored in iron, mild steel or aluminum containers, but copper containers are not suitable because the acetic acid produced by decomposition is corrosive to copper. It is best to store it in a cool, dry and well-ventilated warehouse, away from fire, heat sources and direct sunlight.

 

Poly(Ethylene Glycol) Dicarboxylate/Poly(Ethylene Oxide) Hydrogel Film Co-Crosslinked by Electron Beam Irradiation as an Anti-Adhesion Barrier

 

The cross-linked poly(ethylene glycol) dicarboxylate (PEGDC)/poly(ethylene oxide) (PEO) and poly(ethylene glycol) dimethacrylate (PEGDMA)/(PEO) hydrogels were developed for possible biomedical applications such as an anti-adhesion barrier. Various contents of PEGDC/PEO film were irradiated using an electron beam with various beam intensities in order to obtain various degrees of crosslinked hydrogels. The optimum dose (300 kGy) and total crosslinker content of 10% were used to prepare crosslinked hydrogel films with three different compositions (10% PEGDC, 10% PEGDMA, 5% PEGDC–5% PEGDMA). Among them, 10% PEGDC hydrogel film exhibited the highest elongation at break (69.33 ± 6.87%) with high mechanical strength. 10% PEGDC hydrogel film showed the lowest hemolysis activity (6.03 ± 0.01%) and the highest tissue adherence (75.67 ± 1.15 cN). The result also indicated that the carboxyl groups in PEGDC affect the tissue adherence of hydrogel films via H-bonding interactions. In animal studies, 10% PEGDC anti-adhesion hydrogel film degraded within 3 weeks and demonstrated better anti-adhesive effect compared to Guardix-SG®.

 

Ethylene Glycol Dicarboxylate

Synthesis of Ethylene Glycol and Terephthalic Acid from Biomass for Producing PET

There have been considerable efforts to produce renewable polymers from biomass. Poly(ethylene terephthalate) (PET) is one of the most versatile bulk materials used in our daily lives. Recent advances in the new catalytic process for conversion of biomass have allowed us to design more technically effective and cheaper methods for the synthesis of green PET monomers. This review analyses recent advances in the synthesis of PET monomers from biomass. Different routes for ethylene glycol (EG) and purified terephthalic acid (PTA) synthesis are systematically summarized. The advantages and drawbacks of each route are discussed in terms of feedstock, reaction pathway, catalyst, economic evaluation and technology status, trying to provide some state-of-the-art information on green PET monomer synthesis. Finally, an outlook is presented to highlight the challenges, opportunities and on-going trends, which may serve as guidelines for designing novel synthetic routes to green polymers from fundamental science to practical use.

 

Effect of Molecular Weight of Poly(Ethylene Glycol) Dicarboxylate on the Properties of Cross-Linked Hydrogel Film as an Antiadhesion Barrier
 

Polyethylene glycol dicarboxylate (PEGDC)/polyethylene oxide (PEO) cross-linked hydrogel films were developed using electron beam as an anti-adhesion barrier. The effect of the molecular weight of PEGDC on the properties of hydrogels was studied. Reduction in PEGDC molecular weight increased gel fraction and tissue adhesion without significant changes in mechanical strength. As the molecular weight of PEGDC decreases, the swelling rate decreases rapidly. PEGDC (2000 or 3000) is less cytotoxic, while PEGDC (1000) is more cytotoxic. In animal studies, all hydrogels showed better anti-adhesion effects compared to controls.

 

Physicochemical Properties of Ethylene Glycol

Ethylene glycol with the formula CH2OH2, also known as 1,2-ethanediol, is a popular organic compound. The safety data sheet for ethylene glycol, as well as for other substances, is the primary source of information on their physical and chemical properties. Ethylene glycol is the main component of antifreeze in HVAC and automotive systems. The formula of glycol clearly indicates that it belongs to a chemical group of dihydroxy alcohols, also known as diols. Thus, glycol as an alcohol is a colourless liquid with a high viscosity and a sweet taste. In addition to its excellent miscibility with water, it is also very soluble in aldehydes, ketones and acetic acid, but it does not dissolve at all in carbon tetrachloride. It is relatively cheap to produce. Its disadvantage is crystallisation at low temperatures and lower (compared to propylene glycol) ability to absorb heat (that is about 50% of the heat capacity of water).

 

Ethylene glycol has a high boiling point (197ᵒC) while having a low molecular weight. This is due to the strong association of molecules in the liquid phase, caused by the formation of hydrogen bonds. In its pure form, ethylene glycol freezes at about -13°C, while the ethylene glycol: water mixture can remain liquid at much lower temperatures. A mixture of 40% water and 60% glycol, for example, can withstand temperatures down to about -37ᵒC. It should be noted that ethylene glycol is miscible with water in all proportions. This is due to the presence of two hydroxyl groups in its structure.

 

Synthesis of Ethylene Glycol Dicarboxylate

 

In a 125 mL two-necked round-bottomed flask, add a certain amount of ethylene glycol, glacial acetic acid, dehydration entrainer (such as benzene, toluene, cyclohexane, etc.), catalyst, shake well, then add a few small grains of zeolite, and place it at the mouth of the flask. Connect the moisture separator, and then connect the upper end of the moisture separator to the spherical reflux condenser tube. Install a thermometer on the other end of the flask. Place the flask on an electric stove and heat to reflux. During the reflux process, when the lower liquid level in the water separator is about to reach the branch pipe opening, release 5 mL of accumulated liquid from the lower end, and then continue to reflux. When the lower liquid level in the moisture separator does not change within 10 minutes, then reflux for 30 minutes, remove the moisture separator and spherical condenser tube, connect the straight tube condenser tube, and proceed with distillation (generally reflux for 3 hours) ). In the fraction before the boiling point of the pure dehydration entrainer, add 1% sodium hydroxide solution dropwise to make the fraction neutral. The oil in the upper layer can be considered as the pure dehydration entrainer for use as a pure dehydration entrainer next time. . Collect the 186~192 C fraction to obtain colorless and transparent ethylene glycol diacetate. When using concentrated sulfuric acid as a catalyst, after the photoreaction refluxes for 2 hours, remove the water separator and spherical condenser tube, connect a straight tube condenser tube, distill to 150 C, stop heating, cool, and add people to the flask. 40.mL water, use anhydrous sodium carbonate powder to adjust the pH value of the reaction solution to 7~8, then use a separatory funnel to separate the oil layer (at the bottom of the separation liquid), dry it with anhydrous magnesium sulfate, filter, and the filtrate is distilled , collect the 186~192 C fraction.

 

The Role of Ethylene Glycol in Polycarboxylic Acids
 

Synthetic Raw Materials
Ethylene glycol (Ethylene Glycol) is usually used as one of the raw materials for the synthesis of polycarboxylic acid water-reducing agent. It produces ethylene glycol methacrylate (Methacrylic Acid Ethylene Glycol) through an esterification reaction with acrylic acid or its derivatives. Ester), which is the basic monomer for the preparation of polycarboxylate superplasticizers.

 

Introduction Of Side Chains
Introducing ethylene glycol into the molecular structure of polycarboxylic acid can form hydrophilic side chains. This side chain has a good dispersion effect on cement particles and can reduce the water consumption of concrete mixtures. while maintaining good liquidity.

 

Controlling Performance
By changing the amount, length and ratio of ethanol to other monomers, the molecular weight and distribution of the final polymer product can be adjusted, thereby affecting the performance of the polycarboxylate water-reducing agent, such as water-reducing rate. , slump retention, early and late strength development, etc.

 

Environmentally Friendly
Ethylene glycol is a relatively environmentally friendly raw material, which to a certain extent helps to improve the environmental friendliness of polycarboxylate water-reducing agents, because compared with some traditional naphthalene series and sulfamate Similar water-reducing agents and polycarboxylic acid-based water-reducing agents produce less environmental pollution during production and use.

 

 

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FAQ
 

Q: What is Ethylene Glycol Dicarboxylate?

A: Poly(ethylene glycol) dicarboxylate (PEGDC) contains carboxyl groups that increase the adhesive strength of the film to the tissue. [17,18] A lower molecular weight of PEGDC might improve the mechanical strength and physical properties of hydrogel film due to the higher physical cross-link density.

Q: What are the applications of ethylene glycol dicarboxylate?

A: EGDC is mainly used as a building block to synthesize PET and other copolymers, which are widely used in packaging, textiles, and engineering plastics. It can also be utilized in the production of liquid crystal displays (LCDs) and as a precursor for pharmaceutical intermediates.

Q: How is ethylene glycol dicarboxylate produced?

A: EGDC can be synthesized through various chemical reactions. One common method involves the oxidation of ethylene glycol diacetate, where acetic acid groups are converted into carboxylic acid groups. Another approach involves esterification reactions between ethylene glycol and a suitable dicarboxylic acid or its derivative.

Q: What are the physical and chemical properties of ethylene glycol dicarboxylate?

A: EGDC is typically a white crystalline solid with a melting point around 200°C. It has good thermal stability and is soluble in polar solvents like methanol, ethanol, and acetone. Its chemical structure makes it reactive towards nucleophilic substitution and esterification reactions.

Q: Is ethylene glycol dicarboxylate safe to handle?

A: Like many chemicals, ethylene glycol dicarboxylate should be handled with care. It can pose risks if ingested, inhaled, or comes into contact with skin. Proper personal protective equipment (PPE) should be worn when handling EGDC, and safety data sheets (SDS) should be consulted for specific hazards and precautions.

Q: What are the regulations concerning the use of ethylene glycol dicarboxylate?

A: Regulations regarding the use of ethylene glycol dicarboxylate vary by country and region. Users should familiarize themselves with local environmental, health, and safety regulations to ensure compliance.

Q: What is the chemical formula of Ethylene Glycol Dicarboxylate?

A: Ethylene glycol dimethacrylate is an organic substance with the chemical formula C10H14O4. It is a colorless liquid with a refractive index of 1.4549 and is slightly soluble in water.

Q: What are the applications of ethylene glycol dicarboxylate?

A: EGDC is primarily used as a monomer in the production of polyesters and copolymers for use in films, fibers, and plastics. It is also utilized in the formulation of lubricants, surfactants, and detergents.

Q: How is ethylene glycol dicarboxylate synthesized?

A: EGDC is typically synthesized through the oxidation of ethylene glycol with a suitable oxidizing agent, followed by carboxylation of the resulting hydroxyethylene compound.

Q: What are the physical properties of ethylene glycol dicarboxylate?

A: EGDC is a solid at room temperature with a melting point of approximately 190°C. It is soluble in polar solvents like water and alcohols.

Q: What is the role of ethylene glycol dicarboxylate in the polymer industry?

A: In the polymer industry, EGDC acts as a building block for the creation of various polyesters, which are used in a wide range of applications from packaging to clothing.

Q: What happens when you mix ethylene glycol and water?

A: Pure ethylene glycol freezes at about −12 °C (10.4 °F) but, when mixed with water, the mixture freezes at a lower temperature. For example, a mixture of 60% ethylene glycol and 40% water freezes at −45 °C (−49 °F). Diethylene glycol behaves similarly.

Q: What are the typical reaction conditions for the synthesis of ethylene glycol dicarboxylate?

A: The synthesis of EGDC generally involves controlled reaction conditions, such as specific pH levels, temperatures, and the use of catalysts, to ensure the desired product is formed efficiently.

Q: What are the advantages of ethylene glycol?

A: The manufacture of ink for ballpoint pens and other inks. Ethylene glycol helps increase ink viscosity and makes it less likely to evaporate. Heat transfer fluids such as industrial coolants for gas compressors, heating, ventilating, and air-conditioning systems and ice skating rinks.

Q: What are the common impurities found in commercial samples of ethylene glycol dicarboxylate?

A: Commercial samples of EGDC may contain impurities such as unreacted starting materials, byproducts, or residual catalysts. Purification steps are often required to achieve high purity.

Q: What is the solubility of ethylene glycol dicarboxylate in different solvents?

A: EGDC is highly soluble in polar solvents like water, methanol, and ethanol, but less soluble in non-polar solvents.

Q: What are the safety precautions when handling ethylene glycol dicarboxylate?

A: Personal protective equipment (PPE), such as gloves, safety goggles, and lab coats, should be worn when handling EGDC. Proper ventilation and spill containment measures are also important.

Q: What is the use of ethylene glycol in medicine?

A: They are viscous and colorless liquids. Some are used as anesthetics or hypnotics. However, the class is best known for their use as a coolant or antifreeze. A mild hypnotic used for experimental purposes that was previously used for the treatment of insomnia.

Q: What is the storage stability of ethylene glycol dicarboxylate?

A: EGDC should be stored in a cool, dry place away from heat, light, and moisture to maintain its stability and quality over time.

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