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447315

Sigma-Aldrich

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
Beilstein:
1779069
EC Number:
218-463-4
MDL number:
MFCD00042871
UNSPSC Code:
12162002
PubChem Substance ID:
24868332
NACRES:
NA.23

grade

technical grade

Quality Level

100

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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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
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H411

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

447315-BULK:
447315-VAR:
447315-500ML:
447315-100ML:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP9694
MKCP7106
MKCP2684
MKCK9518
MKCH5359

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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)
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