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About This Item
Linear Formula:
CH2=CHCOOC12H25
CAS Number:
Molecular Weight:
240.38
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
218-463-4
Beilstein/REAXYS Number:
1779069
MDL number:
grade
technical grade
Quality Level
assay
90%
contains
50-200 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
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).
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
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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Grafting polyacrylates on natural rubber latex, by miniemulsion polymerization
Ragupathy L, et al.
Colloid and Polymer Science, 289, 229?235-229?235 (2011)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 447315-100ML | 04061832286938 |
| 447315-500ML | 04061832286952 |

