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About This Item
Linear Formula:
(C10H16O2)n
CAS Number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
MDL number:
InChI
1S/C10H16O2/c1-8(2)10(11)12-9-6-4-3-5-7-9/h9H,1,3-7H2,2H3
InChI key
OIWOHHBRDFKZNC-UHFFFAOYSA-N
SMILES string
CC(=C)C(=O)OC1CCCCC1
form
powder
refractive index
n20/D 1.5065 (lit.)
transition temp
Tg 104 °C
density
1.1 g/mL at 25 °C (lit.)
Quality Level
Related Categories
General description
The four relaxation process (α,β,γ,δ) of poly(cyclohexyl methacrylate) was studied by investigating its viscoelastic and dielectric properties over a range of temperatures.
Application
Poly(cyclohexyl methacrylate (PCHMA) may be used to prepare polymeric blends with polystyrene and nanocomposites with carbon nanotubes. Densely grafted PCHMA on multiwalled carbon nanotubes (MWCNTs) composites exhibits better mechanical properties and electrical resistance compared to PCHMA blended CNTs composites.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Rheological and thermodynamic study of the miscible blend polystyrene/poly (cyclohexyl methacrylate).
Friedrich C, et al.
Polymer, 37(12), 2499-2507 (1996)
Ultrahigh electrical resistance of poly (cyclohexyl methacrylate)/carbon nanotube composites prepared using surface?initiated polymerization.
Hayashida K and Tanaka H
Advances in Functional Materials, 22(11), 2338-2344 (2012)
Dielectric and mechanical-dynamical studies on poly (cyclohexyl methacrylate).
Ribes-Greus A, et al.
Polymer, 26(12), 1849-1854 (1985)
Articles
Self-assembled monolayers (SAMs) have diverse applications; article compares benefits of alkylthiolates on gold SAM systems.
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