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Dimethylaminoethyl methacrylate

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Identification
Molecular formula
C8H15NO2
CAS number
2867-47-2
IUPAC name
2-(dimethylamino)ethyl 2-methylprop-2-enoate
State
State

At room temperature, Dimethylaminoethyl methacrylate is in a liquid state.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
173.00
Boiling point (Kelvin)
446.15
General information
Molecular weight
157.21g/mol
Molar mass
157.2100g/mol
Density
0.9464g/cm3
Appearence

Dimethylaminoethyl methacrylate is a clear, colorless liquid with a slight amine-like odor. It is often used in the polymer industry and can react easily with acids.

Comment on solubility

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

The solubility of 2-(dimethylamino)ethyl 2-methylprop-2-enoate is an important characteristic that affects its behavior in various applications. This compound is known to be a type of amino ester, which generally shows a notable affinity for polar solvents.

  • Water Solubility: The polar nature of the amino group suggests that it may have some degree of solubility in water, especially considering the ethyl moiety, which can interact favorably with water molecules.
  • Solvent Compatibility: It is often more soluble in organic solvents such as methanol, ethanol, and acetone, due to its alkyl groups that enhance solvation in non-polar environments.
  • Effects of Temperature: Generally, the solubility can increase with temperature as molecular interactions become more energetic, facilitating dissolution.

In conclusion, while the specific solubility characteristics of 2-(dimethylamino)ethyl 2-methylprop-2-enoate can vary based on conditions, its structure indicates a propensity towards solubility in both polar and non-polar environments. The interaction of its functional groups plays a critical role, making it an interesting compound for further exploration in chemical applications.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl 2-methylprop-2-enoate

The compound 2-(dimethylamino)ethyl 2-methylprop-2-enoate, often referred to for its distinctive chemical structure and functional groups, is a fascinating compound that is commonly utilized in various fields of chemistry and industry. Here are some captivating aspects of this compound:

  • Versatility in Chemical Reactions: This compound is a versatile intermediate used in the synthesis of various chemical derivatives. Its unique structure allows for easy modification, making it an essential tool for organic chemists.
  • Role in Polymer Chemistry: Derivatives of this compound can be used in the production of polymers, particularly in the creation of materials with specific properties such as flexibility, durability, and responsiveness to stimuli.
  • Biological Activity: The dimethylamino group in its structure is known to impart significant biological activity, which may be useful in pharmaceutical applications. This feature has led researchers to explore its potential as a drug candidate.
  • Importance in Research: The compound has gained attention in research for its potential applications in drug delivery systems, offering enhanced efficiency in targeting specific cells. Its unique characteristics are being investigated for developing innovative therapeutic strategies.
  • Environmental Considerations: As scientists shift their focus toward sustainable practices, compounds like 2-(dimethylamino)ethyl 2-methylprop-2-enoate are evaluated for their environmental impact in various industrial processes, paving the way for greener alternatives.

In summary, 2-(dimethylamino)ethyl 2-methylprop-2-enoate is not only a compound of interest in organic synthesis but also exhibits properties that may lead to advancements in pharmaceuticals and materials science. As research continues, this compound may unveil even more exciting applications and possibilities.

Synonyms
2-(N,N-Dimethylamino)ethyl methacrylate
NSC-20959
2-(Dimethylamino)ethyl methacrylate
2867-47-2
Dimethylaminoethyl methacrylate
Ageflex FM-1
DMAEMA
N,N-DIMETHYLAMINOETHYL METHACRYLATE
USAF RH-3
2-Dimethylaminoethyl methacrylate
2-Propenoic acid, 2-methyl-, 2-(dimethylamino)ethyl ester
2-(dimethylamino)ethyl 2-methylprop-2-enoate
Methacrylic acid, 2-(dimethylamino)ethyl ester
N,N-Dimethylethanolamine methacrylate
NSC 20959
(Dimethylamino)ethyl methacrylate
Ethanol, 2-(dimethylamino)-, methacrylate
O0V97PV2G1
DTXSID1027504
2-Dimethylaminoethylester kyseliny methakrylove
N,N-(Dimethylamino)ethyl methacrylate
.beta.-(Dimethylamino)ethyl methacrylate
2-(Dimethylamino)ethyl methacrylate (stabilized with MEHQ)
.beta.-(N,N-Dimethylamino)ethyl methacrylate
Methacrylic acid 2-(dimethylamino)ethyl ester
2-(Dimethylamino)ethyl Methacrylate (Stabilized with 0.2% 4-methoxyphenol)
CCRIS 872
HSDB 5464
beta-Dimethylaminoethyl methacrylate
EINECS 220-688-8
UN2522
BRN 1757048
UNII-O0V97PV2G1
Basic Butylated Methacrylate Copolymer Imp. C (EP); 2-(Dimethylamino)ethyl Methacrylate; Basic Butylated Methacrylate Copolymer Impurity C
MFCD00008589
Ethanol, methacrylate
2-Dimethylaminoethylester kyseliny methakrylove [Czech]
2-(Dimethylamino)ethyl 2-methyl-2-propenoate
EC 220-688-8
dimethylaminoethylmethacrylate
Sipomer 2M1M (Salt/Mix)
SCHEMBL14984
4-04-00-01432 (Beilstein Handbook Reference)
DTXCID307504
CHEMBL1883484
WLN: 1UY1&VO2N1&1
NSC20959
N,N-di-methylaminoethyl methacrylate
Tox21_201694
methacryloyloxyethyl-N,N-dimethylamine
AKOS005207198
2-(dimethylamino)ethyl methylpropenoate
AT33769
FD37322
UN 2522
NCGC00164097-01
NCGC00164097-02
NCGC00259243-01
LS-13486
2-(Dimethylamino)ethyl 2-methylacrylate #
CAS-2867-47-2
M0082
NS00002830
N,N-DIMETHYLAMINOETHYL METHACRYLATE [HSDB]
Q27285181
2-Dimethylaminoethyl methacrylate [UN2522] [Poison]
2-methyl-2-propenoic acid 2-(dimethylamino)ethyl ester
2-(Dimethylamino)ethyl Methacrylate, (stabilized with MEHQ)
2-(Dimethylamino)ethyl Methacrylate (Stabilized with 0.2per cent 4-methoxyphenol)
2-(Dimethylamino)ethyl methacrylate, European Pharmacopoeia (EP) Reference Standard
2-(Dimethylamino)ethyl methacrylate, contains 700-1000 ppm monomethyl ether hydroquinone as inhibitor, 98%