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Merck
CN

447315

Lauryl acrylate

technical grade, 90%

Synonym(s):

Dodecyl acrylate

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About This Item

Linear Formula:
CH2=CHCOOC12H25
CAS Number:
2156-97-0
Molecular Weight:
240.38
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24868332
EC Number:
218-463-4
Beilstein/REAXYS Number:
1779069
MDL number:
MFCD00042871

Key Documents

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Product Name

Lauryl acrylate, technical grade, 90%

InChI key

PBOSTUDLECTMNL-UHFFFAOYSA-N

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

SMILES string

CCCCCCCCCCCCOC(=O)C=C

grade

technical grade

assay

90%

refractive index

n20/D 1.445 (lit.)

density

0.884 g/mL at 25 °C (lit.)

contains

50-200 ppm monomethyl ether hydroquinone as inhibitor

Quality Level

100

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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).

General description

Lauryl acrylate monomers are extremely hydrophobic in nature.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ2893
MKCW9121
MKCW0585
MKCT8553
MKCT2203

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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)
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)
Grafting polyacrylates on natural rubber latex, by miniemulsion polymerization
Ragupathy L, et al.
Colloid and Polymer Science, 289, 229?235-229?235 (2011)
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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