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Octadecyl acrylate

Basic information Safety Supplier Related

Octadecyl acrylate Basic information

Product Name:
Octadecyl acrylate
Synonyms:
  • 2-Propenoicacid,octadecylester
  • Octadecyl2-propenoate
  • octadecylacrylate(stearylacrylate)
  • STEARYL ACRYLATE
  • Octadecyl acrylate Factory COA TDS MSDS
  • N-OCTADECYL ACRYLATE
  • OCTADECYL ACRYLATE
  • Octadecylacrylat
CAS:
4813-57-4
MF:
C21H40O2
MW:
324.54
EINECS:
225-383-3
Product Categories:
  • Functional Monomer
  • 4813-57-4
Mol File:
4813-57-4.mol
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Octadecyl acrylate Chemical Properties

Melting point:
32-34 °C (lit.)
Boiling point:
402.85°C (rough estimate)
Density 
0.8 g/mL at 25 °C (lit.)
vapor pressure 
0.001Pa at 25℃
refractive index 
1.5344 (estimate)
Flash point:
>230 °F
solubility 
Insoluble in water
form 
powder to lump to clear liquid
color 
White or Colorless to Almost white or Almost colorless
Water Solubility 
260.9ng/L at 25℃
InChIKey
FSAJWMJJORKPKS-UHFFFAOYSA-N
LogP
9.08 at 25℃
CAS DataBase Reference
4813-57-4(CAS DataBase Reference)
NIST Chemistry Reference
Octadecyl acrylate(4813-57-4)
EPA Substance Registry System
Stearyl acrylate (4813-57-4)
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Safety Information

Hazard Codes 
Xi,N
Risk Statements 
41-51/53-36/37/38-43-38
Safety Statements 
26-39-61-36/37/39
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
2
TSCA 
TSCA listed
HS Code 
29161290

MSDS

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Octadecyl acrylate Usage And Synthesis

Description

Octadecyl acrylate is a versatile monomer extensively utilized in synthesizing polymer materials. It presents as a colorless and viscoelastic liquid. Its wide-ranging applications encompass coatings, adhesives, sealants, and printing inks, making it an indispensable ingredient in the polymer industry. Notably, Octadecyl acrylate contributes to the production of polymers used in various medical applications and the manufacturing of polyurethane foams. It serves as a valuable model for studying polymerization reactions, offering insights into the properties of polymer materials. During the polymerization process, Octadecyl acrylate undergoes a crucial reaction. This reaction involves the formation of covalent bonds between the monomer molecules. Precisely, addition polymerization occurs, where a monomer molecule adds to a double bond between two other monomer molecules, establishing the covalent bonds that create the polymer material.

Uses

stearyl acrylate is generally found in combination with other chemicals, it acts as a film former to help maintain moisture in the skin.

Uses

Octadecyl Acrylate is a reagent used in the synthesis of comb-like polymers which are incorporated into waterborne latexes improving barrier properties.

Application

Octadecyl acrylate undergoes surface-initiated atom transfer radical polymerization (ATRP) to form poly(octadecyl acrylate). ODA can form copolymers with cinnamoyloxy ethyl methacrylate (CEMA).

Flammability and Explosibility

Non flammable

References

[1] Stephan A. Letts, Tomlinson Fort. “Polymerization of Oriented Monolayers of Octadecyl Acrylate.” Journal of Colloid and Interface Science 202 2 (1998): Pages 341-347.
[2] Miao Yao, Yong He*, Jun Nie. “Can Chain-Reaction Polymerization of Octadecyl Acrylate Occur in Crystal?” Macromolecules 51 10 (2018): 3731–3737.

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