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447315

Sigma-Aldrich

Lauryl acrylate

technical grade, 90%

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Synonym(s):
Dodecyl acrylate
Linear Formula:
CH2=CHCOOC12H25
CAS Number:
Molecular Weight:
240.38
Beilstein:
1779069
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.23

grade

technical grade

Quality Level

Assay

90%

contains

60-100 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.445 (lit.)

density

0.884 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCOC(=O)C=C

InChI

1S/C15H28O2/c1-3-5-6-7-8-9-10-11-12-13-14-17-15(16)4-2/h4H,2-3,5-14H2,1H3

InChI key

PBOSTUDLECTMNL-UHFFFAOYSA-N

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234923407348408298
Lauryl acrylate technical grade, 90%

Sigma-Aldrich

447315

Lauryl acrylate

Butyl acrylate ≥99%, contains 10-60 ppm monomethyl ether hydroquinone as inhibitor

Sigma-Aldrich

234923

Butyl acrylate

assay

90%

assay

≥99%

assay

-

assay

≥ 85.0%

contains

60-100 ppm monomethyl ether hydroquinone as inhibitor

contains

10-60 ppm monomethyl ether hydroquinone as inhibitor

contains

150-350 ppm MEHQ as inhibitor

contains

1000 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.445 (lit.)

refractive index

n20/D 1.418 (lit.)

refractive index

n20/D 1.502

refractive index

n20/D 1.439 (lit.)

density

0.884 g/mL at 25 °C (lit.)

density

0.894 g/mL at 25 °C (lit.)

density

1.127 g/mL at 25 °C

density

1.016 g/mL at 25 °C (lit.)

General description

Lauryl acrylate monomers are extremely hydrophobic in nature.

Application

Lauryl acrylate can undergo atom transfer radical polymerization (ATRP) to form its polymer. Lauryl acrylate may undergo photoinitiated polymerization in the presence of N-acetyl-4-nitro-1-naphthylamine (ANNA) and N,N-dimethylaniline (DMA).

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The atom transfer radical polymerization of lauryl acrylate.
Beers KL and Matyjaszewski K
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 38(7) (2001)
Grafting polyacrylates on natural rubber latex, by miniemulsion polymerization
Ragupathy L, et al.
Colloid and Polymer Science, 289, 229?235-229?235 (2011)
Photoinitiated bulk polymerization of lauryl acrylate by N-acetyl-4-nitro-1-naphthylamine in the presence of N,N-dimethylaniline
Sastre R, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 44(1), 111-122 (1988)
Shihong Deng et al.
Advanced materials (Deerfield Beach, Fla.), 31(39), e1903970-e1903970 (2019-08-14)
3D printing has witnessed a new era in which highly complexed customized products become reality. Realizing its ultimate potential requires simultaneous attainment of both printing speed and product versatility. Among various printing techniques, digital light processing (DLP) stands out in
Fulvio Grigolato et al.
ACS nano, 11(11), 11358-11367 (2017-10-19)
Interactions between proteins and surfaces in combination with hydrodynamic flow and mechanical agitation can often trigger the conversion of soluble peptides and proteins into aggregates, including amyloid fibrils. Despite the extensive literature on the empirical effects of surfaces and mechanical

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