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291811

Sigma-Aldrich

Lauryl methacrylate

contains 500 ppm MEHQ as inhibitor, 96%

Synonym(s):

Dodecyl 2-methyl-2-propenoate, Dodecyl methacrylate

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About This Item

Linear Formula:
CH2=C(CH3)COO(CH2)11CH3
CAS Number:
142-90-5
Molecular Weight:
254.41
Beilstein/REAXYS Number:
1708160
EC Number:
205-570-6
MDL number:
MFCD00008972
UNSPSC Code:
12162002
PubChem Substance ID:
24857542
NACRES:
NA.23

Quality Level

200

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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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
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
Zacharoula Iatridi et al.
ACS applied materials & interfaces, 8(51), 35059-35070 (2016-12-15)
Adequately designed multiresponsive water-soluble graft copolymers were used to serve as a multifunctional polymeric platform for the encapsulation and transfer in aqueous media of hydrophobic magnetic nanoparticles (MNPs). The backbone of the graft copolymers was composed of hydrophilic sodium methacrylate
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