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Poly(ethylene glycol) dimethacrylate

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Identification
Molecular formula
C13H22O6
CAS number
25852-47-5
IUPAC name
2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate
State
State

At room temperature, this compound is typically in a liquid state. Its viscous nature allows it to be used effectively in polymerization processes.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
286.33g/mol
Molar mass
286.3270g/mol
Density
1.1000g/cm3
Appearence

Poly(ethylene glycol) dimethacrylate is generally a colorless, viscous liquid. It is often used as a crosslinking agent in the production of polymers and resins. The liquid form can appear clear to slightly yellowish, depending on purity and storage conditions.

Comment on solubility

Solubility of 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate

The solubility of 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate is influenced by its unique chemical structure, which incorporates both hydrophobic and hydrophilic features. Understanding its solubility is essential for various applications, especially in the manufacturing and formulation of products. Here are some key points to consider:

  • Hydrophobic Characteristics: The presence of large hydrocarbon groups tends to make the compound less soluble in water, which could lead to precipitation in aqueous environments.
  • Hydrophilic Components: The ethoxy groups introduce some polar characteristics, which may enhance solubility in certain solvents, particularly those that are moderately polar.
  • Solvent Polarity: Solubility generally increases in solvents that match the polar/nonpolar balance, suggesting compatibility with organic solvents such as ethanol, acetone, or chloroform.
  • Temperature Effects: Like many organic compounds, solubility can be temperature-dependent. As the temperature increases, solubility might increase for some solvents due to enhanced molecular motion.

In conclusion, while 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate may face challenges in aqueous solubility, its behavior in organic solvents emphasizes its versatility. As stated, "The balance between hydrophilic and hydrophobic influences sets the stage for solubility behaviors." Understanding these factors can aid in optimizing the use of this compound in various formulations.

Interesting facts

Interesting Facts about 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate

2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate is a fascinating compound that exemplifies the complexity and diversity of organic chemistry. Here are some intriguing aspects of this compound:

  • Functional Groups: This compound features multiple functional groups, which enhances its chemical reactivity. The presence of ester and alkene groups contributes to its unique properties and potentials in various applications.
  • Polymerization Potential: Due to its unsaturated double bonds (alkene groups), this compound is capable of participating in polymerization reactions. This allows it to be used in the development of advanced materials, such as coatings, adhesives, and sealants.
  • Applications in Coatings: Given its chemical structure, this compound is likely to be useful in producing high-performance coatings. Its ability to form cross-linked networks can provide durability and resistance to environmental factors.
  • Synthetic Versatility: The esters and ethers within the molecular framework provide routes for further chemical modifications, leading to a variety of derivatives that can be tailored for specific uses.
  • Research Interest: Compounds like this one are often the subject of research due to their potential in fields such as material science, biomaterials, and nanotechnology. Chemists are continually exploring their properties to unlock new applications.

In conclusion, 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate represents a class of compounds that not only serves as a building block for larger molecules but also holds promise in technological advancements. As researchers delve deeper, the potential applications of this compound are likely to expand significantly.

Synonyms
Diethylene glycol dimethacrylate
2358-84-1
Diethyleneglycol dimethacrylate
Di(ethylene glycol) dimethacrylate
DGM 2
Oxydiethylene methacrylate
TGM 2
Light Ester 2EG
Blemmer PDE 100
CCRIS 7050
HSDB 5458
2,2'-Oxybisethanol Dimethacrylate
DIETHYLENE GLYCOL BIS(METHACRYLATE)
EINECS 219-099-9
Methacrylic acid, oxydiethylene ester
Oxydi-2,1-ethanediyl bismethacrylate
2-Propenoic acid, 2-methyl-, oxydi-2,1-ethanediyl ester
R42PUI926F
DTXSID8044882
DTXCID6024882
Diethylene glycol, dimethacrylate
DIETHYLENE GLYCOL BIS(METHACRYLATE) [HSDB]
METHACRYLIC ACID, DIESTER WITH DIETHYLENE GLYCOL
DEGDMA
Oxydi2,1ethanediyl bismethacrylate
DIETHYLENE GLYCOL DIMETHACRYLATE [INCI]
2Propenoic acid, 2methyl, oxydi2,1ethanediyl ester
2Propenoic acid, 2methyl, 1,1'(oxydi2,1ethanediyl) ester
2-propenoic acid, 2-methyl-, 1,1'-(oxydi-2,1-ethanediyl) ester
Oxybis(ethane-2,1-diyl) bis(2-methylacrylate)
129011-76-3
2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate
Diethylene glycol dimethacrylate monomer
25101-18-2
Diethylene glycol dimethacrylate(8 cp(20 degrees c))
UNII-R42PUI926F
2,2'-Oxydiethyl Dimethacrylate
Ageflex DEGDMA
MFCD00014931
SCHEMBL24260
CHEMBL3186638
MFM-418
Tox21_301734
3-Oxapentane-1,5-diyl dimethacrylate
AKOS015903120
CS-W010276
HY-W009560
Di(ethylene glycol) dimethacrylate, 95%
Di(ethylene glycol) dimethacrylate, 96%
NCGC00256100-01
BS-48957
CAS-2358-84-1
D1530
NS00010758
Oxybis(ethane-2,1-diyl)bis(2-methylacrylate)
E82986
Q27287772
2-[2-(Methacryloyloxy)ethoxy]ethyl 2-methylacrylate #
Diethylene Glycol Dimethacrylate (stabilized with MEHQ)
Diethylene Glycol Dimethacrylate, (stabilized with MEHQ)
2-Methyl-2-propenoic acid oxidi-2,1-ethanediyl ester,homopolymer
2-{2-[(2-methylprop-2-enoyl)oxy]ethoxy}ethyl 2-methylprop-2-enoate