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Key Documents

291811

Sigma-Aldrich

Lauryl methacrylate

contains 500 ppm MEHQ as inhibitor, 96%

Sinônimo(s):

Dodecyl 2-methyl-2-propenoate, Dodecyl methacrylate

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About This Item

Fórmula linear:
CH2=C(CH3)COO(CH2)11CH3
Número CAS:
Peso molecular:
254.41
Beilstein:
1708160
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de substância PubChem:
NACRES:
NA.23

Ensaio

96%

contém

500 ppm MEHQ as inhibitor

índice de refração

n20/D 1.445 (lit.)

pb

142 °C/4 mmHg (lit.)

pf

−7 °C (lit.)

densidade

0.868 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

GMSCBRSQMRDRCD-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Pictogramas

Exclamation markEnvironment

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

224.6 °F - closed cup

Ponto de fulgor (°C)

107 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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The Fabrication of Very Small Miniemulsion Latexes from N-Stearoylglutamate and Lauryl Methacrylate: Evidence for Droplet Budding
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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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