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Dimethylaminoethyl methacrylate

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Identification
Molecular formula
C8H15NO2
CAS number
2867-47-2
IUPAC name
2-(dimethylamino)ethyl prop-2-enoate
State
State
This compound is in a liquid state at room temperature. It is generally stored in airtight containers due to its sensitivity to air and moisture.
Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
157.21g/mol
Molar mass
157.2110g/mol
Density
0.9496g/cm3
Appearence

Dimethylaminoethyl methacrylate is a clear, colorless liquid. It has a distinct amine-like odor. This liquid is commonly used in polymer synthesis due to its reactivity with acids and ability to form polymers.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl prop-2-enoate

The solubility of 2-(dimethylamino)ethyl prop-2-enoate, also known as a zwitterionic compound, is noteworthy due to its unique structural features. Its solubility is significantly influenced by various factors, including its functional groups and the solvent used. Here are some key points to consider:

  • Polarity: The presence of the dimethylamino group enhances the compound's polarity, allowing it to dissolve well in polar solvents such as water.
  • Hydrogen Bonding: The ability of the dimethylamino group to participate in hydrogen bonding further contributes to improved solubility in aqueous environments.
  • Hydrophobic Character: The prop-2-enoate portion introduces some hydrophobic characteristics, which can impact solubility in non-polar solvents.
  • Temperature Effects: Like many chemical compounds, the solubility of 2-(dimethylamino)ethyl prop-2-enoate increases with temperature, making it more favorable for dissolution at elevated temperatures.

In summary, the solubility of 2-(dimethylamino)ethyl prop-2-enoate is enhanced by its polar characteristics and ability to form hydrogen bonds. It is particularly soluble in polar solvents, with solubility behavior that can be further modulated by temperature and solvent interactions.

Interesting facts

Interesting Facts About 2-(Dimethylamino)ethyl Prop-2-enoate

2-(Dimethylamino)ethyl prop-2-enoate, often referred to by its more common name, is a fascinating compound in the realm of chemistry. This compound exhibits a range of intriguing properties and applications that make it significant in various fields.

Chemical Structure and Properties

This compound features a vinyl group, which lends it unique reactivity. Some noteworthy points include:

  • Reactive Monomer: The compound can polymerize, making it useful in the production of polymers and resins.
  • Nucleophilicity: The dimethylamino group enhances the nucleophilic character of the molecule, allowing it to participate in a variety of chemical reactions.
  • Hydrophilicity: The presence of the amino group increases its solubility in polar solvents, expanding its applications in different environments.

Applications in Industry

2-(Dimethylamino)ethyl prop-2-enoate is utilized in numerous industries:

  • Coatings: Its ability to form strong bonds makes it ideal for coatings that require durability.
  • Adhesives: The compound is often a component in adhesives due to its adhesive properties when polymerized.
  • Biomedical Applications: Research is ongoing into its potential use in drug delivery systems, owing to its ability to modify interactions with biological membranes.

Safety and Handling

As with many chemical compounds, safety is a priority:

  • Personal Protective Equipment (PPE): Always wear appropriate PPE such as gloves and goggles when handling this compound.
  • Ventilation: Work in a well-ventilated area to avoid inhalation of vapors.

In summary, 2-(dimethylamino)ethyl prop-2-enoate is not just an ordinary chemical compound; it is a vital building block in various chemical reactions and industrial applications. Its unique structure and reactivity open doors for innovation in synthetic applications and materials science.

Synonyms
2-(DIMETHYLAMINO)ETHYL ACRYLATE
2439-35-2
Dimethylaminoethyl acrylate
N,N-Dimethylaminoethyl acrylate
Adame
2-Propenoic acid, 2-(dimethylamino)ethyl ester
Acrylic acid, 2-(dimethylamino)ethyl ester
NSC 20952
CCRIS 4797
EINECS 219-460-0
5YES121FTL
2-Dimethylaminoethyl acrylate
BRN 1099119
DTXSID5025100
NORSOCRYL ADAME
AI3-08751
NSC-20952
DTXCID705100
EC 219-460-0
ACRYLOYLOXYETHYLDIMETHYLAMINE
DIMETHYLAMINO)ETHYL ACRYLATE, 2-(
(2-(ACRYLOYLOXY)ETHYL)DIMETHYLAMINE
219-460-0
2-(dimethylamino)ethyl prop-2-enoate
2-(N,N-dimethylamino)ethyl acrylate
Dimethylaminoethyl acrylate(1.3 cp)
Ageflex FA-1
dimethylaminoethylacrylate
UNII-5YES121FTL
2-dimethylaminoethyl prop-2-enoate
MFCD00038233
SCHEMBL15115
CHEMBL2135857
DPBJAVGHACCNRL-UHFFFAOYSA-
acryloyloxyethyl-N,N-dimethylamine
NSC20952
Tox21_200307
AKOS005207197
2-(Dimethylamino)ethyl acrylate, 99%
CS-W016416
NCGC00091752-01
NCGC00091752-02
NCGC00257861-01
Acrylic acid, 2-dimethyl aminoethyl ester
BS-42346
Acrylic Acid 2-(Dimethylamino)ethyl Ester
CAS-2439-35-2
A1235
NS00001817
D78266
Q15632909
2-(Dimethylamino)ethyl Acrylate (stabilized with MEHQ)
2-(Dimethylamino)ethyl Acrylate, (stabilized with MEHQ)
2-(DIMETHYLAMINO)ETHYL ACRYLATE(STABILIZED WITH MEHQ)
2-(Dimethylamino)ethyl acrylate, contains <2,000 ppm MEHQ as inhibitor, 98%
InChI=1/C7H13NO2/c1-4-7(9)10-6-5-8(2)3/h4H,1,5-6H2,2-3H3