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291811

Sigma-Aldrich

Lauryl methacrylate

contains 500 ppm MEHQ as inhibitor, 96%

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Synonym(s):
Dodecyl 2-methyl-2-propenoate, Dodecyl methacrylate
Linear Formula:
CH2=C(CH3)COO(CH2)11CH3
CAS Number:
Molecular Weight:
254.41
Beilstein:
1708160
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Assay

96%

contains

500 ppm MEHQ as inhibitor

refractive index

n20/D 1.445 (lit.)

bp

142 °C/4 mmHg (lit.)

mp

−7 °C (lit.)

density

0.868 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCOC(=O)C(C)=C

InChI

1S/C16H30O2/c1-4-5-6-7-8-9-10-11-12-13-14-18-16(17)15(2)3/h2,4-14H2,1,3H3

InChI key

GMSCBRSQMRDRCD-UHFFFAOYSA-N

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This Item
169919447315347485
Lauryl methacrylate contains 500 ppm MEHQ as inhibitor, 96%

Sigma-Aldrich

291811

Lauryl methacrylate

Isobutyl methacrylate 97%

Sigma-Aldrich

169919

Isobutyl methacrylate

Lauryl acrylate technical grade, 90%

Sigma-Aldrich

447315

Lauryl acrylate

contains

500 ppm MEHQ as inhibitor

contains

≤15 ppm monomethyl ether hydroquinone as inhibitor

contains

60-100 ppm monomethyl ether hydroquinone as inhibitor

contains

≤100 ppm BHT as inhibitor

refractive index

n20/D 1.445 (lit.)

refractive index

n20/D 1.420 (lit.)

refractive index

n20/D 1.445 (lit.)

refractive index

n20/D 1.428 (lit.)

bp

142 °C/4 mmHg (lit.)

bp

155 °C (lit.)

bp

-

bp

-

mp

−7 °C (lit.)

mp

-

mp

-

mp

-

density

0.868 g/mL at 25 °C (lit.)

density

0.886 g/mL at 25 °C (lit.)

density

0.884 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

General description

Lauryl methacrylate is a monomer that belongs to the class of methacrylate esters, is extensively employed in the manufacturing of diverse polymer materials. Polymers derived from lauryl methacrylate can be employed in personal care products, where they contribute to the formulation′s rheology, stability, and film-forming properties.

Application

Lauryl methacrylate can be used as a monomer:
  • To prepare polymeric co-stabilizer by free-radical copolymerization.
  • To fabricate fluorine-less superhydrophobic cotton fabrics via graft polymerization process.
  • In the synthesis of prepolymers that are used in oil absorbents.
It can also be used to prepare organic polymeric monolithic columns for capillary electrochromatography. Lauryl methacrylate along with dibutyl itaconate used to synthesize copolymers via emulsion polymerization. The copolymers formed from these monomers are specifically targeted for the development of sustainable pressure-sensitive adhesives. It is also used in the fabrication of asymmetrically superhydrophobic cotton fabrics via the mist polymerization process. As a result, the incorporation of lauryl methacrylate through mist polymerization enables the creation of asymmetrically superhydrophobic cotton fabrics, which find potential applications in self-cleaning textiles, water-resistant coatings, and other related fields.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

224.6 °F - closed cup

Flash Point(C)

107 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Comparison of thermal and photo polymerization of lauryl methacrylate monolithic columns for CEC
Bernabe Zafon V, et al.
Electrophoresis, 30(11), 1939-1936 (2009)
Efficiency of ligands in atom transfer radical polymerization of lauryl methacrylate and block copolymerization with methyl methacrylate
Raghunadh VD, et al.
Polymer, 45(10), 3149-3155 (2004)
Zheng Xing et al.
Physical chemistry chemical physics : PCCP, 19(32), 21426-21435 (2017-08-02)
This work investigates the effect of atmosphere on pyrolysis of a polymer matrix (precursor) for directing its transformation towards more disordered graphene species and smaller graphitic nanograins. These two structural characteristics are crucial to the generation of nano-channels (NCs) pertinent
The Fabrication of Very Small Miniemulsion Latexes from N-Stearoylglutamate and Lauryl Methacrylate: Evidence for Droplet Budding
Yildiz U, et al.
Macromolecular Chemistry and Physics, 204(16), 1966-1970 (2003)
Dennis L Waldron et al.
Nanotechnology, 28(9), 095205-095205 (2017-01-07)
The results are presented for luminescent solar concentrators (LSCs) fabricated with poly(lauryl methacrylate-co-ethylene glycol dimethacrylate) (P(LMA-co-EGDMA)) and Angstrom Bond, Inc. AB9093 acrylic epoxy matrix, high quantum yield (> 70%) PbSe quantum dots (QDs) and silicon photovoltaic (Si PV) cells. LSCs

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