Skip to main content

Lauroyl methacrylate

ADVERTISEMENT
Identification
Molecular formula
C16H30O2
CAS number
142-90-5
IUPAC name
dodecyl 2-methylprop-2-enoate
State
State
At room temperature, lauroyl methacrylate is generally in a liquid state due to its relatively low melting point of -12°C. It can be described as a clear and slightly viscous liquid.
Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
254.41g/mol
Molar mass
254.4130g/mol
Density
0.8777g/cm3
Appearence

Lauroyl methacrylate is generally a colorless or pale yellow liquid. It is clear and has a characteristically acrid odor. The compound may appear as viscous due to its liquid state at room temperature.

Comment on solubility

Solubility of Dodecyl 2-methylprop-2-enoate

Dodecyl 2-methylprop-2-enoate, a compound with a long hydrophobic alkyl chain, exhibits intriguing solubility characteristics. Its solubility can be influenced by various factors:

  • Polarity: The compound is largely non-polar due to its dodecyl group, which makes it less soluble in polar solvents such as water.
  • Solvent Type: It tends to be soluble in non-polar organic solvents like hexane or chloroform, where similar non-polar interactions occur.
  • Temperature Effects: Increasing temperature can enhance solubility in organic solvents as it disrupts intermolecular forces, allowing for better interaction.
  • Concentration:** The degree of solubility is also dependent on the concentration of the solvent; higher concentrations may lead to saturation of the solute.

To summarize, dodecyl 2-methylprop-2-enoate is largely insoluble in water but finds a suitable environment in non-polar organic solvents. The unique structure of this compound imparts distinctive solubility traits that can be leveraged in various applications.

Interesting facts

Interesting Facts about Dodecyl 2-methylprop-2-enoate

Dodecyl 2-methylprop-2-enoate, a fascinating compound, is a type of alkyl methacrylate that offers an array of intriguing properties and applications in the field of chemistry.

Chemical Characteristics

  • Versatile Monomer: This compound can be polymerized to form various types of polymers, which are used in many industrial applications.
  • Hydrophobic Nature: Its long dodecyl chain makes it highly hydrophobic, lending itself to applications in surface modification and coatings.
  • Reactivity: As an unsaturated ester, it can readily undergo copolymerization with other monomers, allowing for the design of materials with tailored properties.

Applications

  • Coatings and Adhesives: Dodecyl 2-methylprop-2-enoate is often utilized in the production of adhesives and coatings due to its excellent bonding characteristics.
  • Biomedical Uses: Its biocompatibility makes it a candidate for biomedical applications, particularly in drug delivery systems.
  • Surface Modifications: The compound is instrumental in modifying surfaces to enhance water repellency and reduce friction.

Fun Facts

  • The term "dodecyl" refers to a twelve-carbon alkyl chain, showcasing the compound's structural complexity.
  • It is part of the methacrylate family, which is known for its widespread use in producing acrylic glass and other clear plastics.
  • In studies, polymers derived from this compound have shown remarkable strength and durability, making them suitable for various engineering applications.

As a long-chain alkyl methacrylate, dodecyl 2-methylprop-2-enoate demonstrates the significant impact that small structural variations can have on the overall properties of polymers. Its potential for innovation in diverse fields continues to be a subject of research among scientists and industry professionals alike.

Synonyms
Dodecyl methacrylate
142-90-5
LAURYL METHACRYLATE
Dodecyl 2-methylacrylate
2-Propenoic acid, 2-methyl-, dodecyl ester
Metazene
N-Dodecyl methacrylate
Dodecyl 2-methyl-2-propenoate
dodecyl 2-methylprop-2-enoate
Sipomer LMA
LAMA
Ageflex FM 246
Methacrylic acid, lauryl ester
GE 410 (methacrylate)
Methacrylic acid, dodecyl ester
Caswell No. 521
Dodecyl-2-methylacrylate
Laurylester kyseliny methakrylove
NSC 5188
SR 313
Acrylic acid, 2-methyl-, dodecyl ester
HSDB 5417
EINECS 205-570-6
EPA Pesticide Chemical Code 053101
UNII-B6L83074BZ
BRN 1708160
n-Lauryl methacrylate
AI3-08765
B6L83074BZ
NSC-5188
2-Methyl-2-propenoic acid, dodecyl ester
Methacrylic Acid Dodecyl Ester
DTXSID4027103
EC 205-570-6
Dodecyl methacrylate (stabilized with MEHQ)
DTXCID107103
Laurylmethacrylate
CAS-142-90-5
LMA
C16H30O2
Laurylester kyseliny methakrylove [Czech]
MFCD00008972
Ageflex FM-12
1-Dodecyl methacrylate
1-Dodecanol methacrylate
Lauryl methacrylate(LMA)
Dodecyl 2-methylacrylate #
SCHEMBL14995
WLN: 12OVYU1
Methacrylic Acid Lauryl Ester
EPA pesticide code 053101
CHEMBL1903701
NSC5188
Tox21_201903
Tox21_303316
N-DODECYL METHACRYLATE [HSDB]
AKOS015903634
CS-W012588
Methyl-2-propenoic acid, dodecyl ester
USEPA/OPP Pesticide Code: 053101
2-methyl-2-propenoic acid dodecyl ester
Lauryl methacrylate(5cp(25 degrees c))
NCGC00164408-01
NCGC00164408-02
NCGC00257059-01
NCGC00259452-01
170292-57-6
AS-76599
Propenoic acid, 2-methyl-, dodecyl ester
DB-042652
Dodecyl ester of 2-methyl-2-propenoic acid
M0083
NS00004091
Dodecyl Methacrylate, (stabilized with MEHQ)
Lauryl methacrylate, purum, >=95.0% (GC)
E75856
LAURYL METHACRYLATE(STABILIZED WITH MEHQ)
Q3395664
Lauryl methacrylate, contains 500 ppm MEHQ as inhibitor, 96%