705314
Poly(glycidyl methacrylate)
Mn 10,000-20,000
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About This Item
Formule linéaire :
[C7H10O3]n
Numéro CAS:
Numéro MDL:
Code UNSPSC :
12162002
Nomenclature NACRES :
NA.23
Produits recommandés
Forme
solid
Niveau de qualité
Poids mol.
Mn 10,000-20,000
Indice de réfraction
n20/D 1.381
Pf
274-280 °C
InChI
1S/C7H10O3/c1-5(2)7(8)10-4-6-3-9-6/h6H,1,3-4H2,2H3
Clé InChI
VOZRXNHHFUQHIL-UHFFFAOYSA-N
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Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Eye Irrit. 2
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Ran Tao et al.
Langmuir : the ACS journal of surfaces and colloids, 28(48), 16580-16587 (2012-11-15)
Initiated chemical vapor deposition (iCVD) of poly(glycidyl methacrylate) from supersaturated monomer vapor is reported. Rapid film growth rates, up to 600 nm/min, were observed. Films grown from supersaturated monomer exhibited distinct surface undulations. The temporal evolution of surface features during
Peng Tao et al.
ACS applied materials & interfaces, 3(9), 3638-3645 (2011-08-10)
Visibly highly transparent indium tin oxide (ITO)/epoxy nanocomposites were prepared by dispersing polyglycidyl methacrylate (PGMA) grafted ITO nanoparticles into a commercial epoxy resin. The oleic acid stabilized, highly crystalline, and near monodisperse ITO nanoparticles were synthesized via a nonaqueous synthetic
Y Hu et al.
ACS applied materials & interfaces, 5(3), 703-712 (2012-12-29)
The biocleavable star-shaped vectors (CD-SS-PGEAs) consisting of nonionic β-cyclodextrin (β-CD) cores and disulfide-linked low-molecular-weight poly(glycidyl methacrylate) (PGMA) derivative arms with plentiful flanking secondary amine and hydroxyl groups were successfully proposed for highly efficient gene delivery. A simple two-step method was
Ying Shen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(43), 13755-13761 (2012-09-19)
The development of magnetic nanoparticles with multiple functions has been an ever-growing field because of their diverse applications in drug delivery, biosensing, cell labeling, and so on. In this study, a facile method was developed to construct multifunctional magnetic nanocomposites.
Peggy Scholtysek et al.
Langmuir : the ACS journal of surfaces and colloids, 28(44), 15651-15662 (2012-10-11)
Semitelechelic poly(glycerol methacrylate)s having a perfluoroalkyl end group (PGMA(n)-F(9)) were synthesized by ATRP. The interactions of these polymers with different degrees of polymerization with chiral or racemic dipalmitoylphosphatidylcholine (l-DPPC, d-DPPC, or rac-DPPC) monolayers at the air/water interface were studied. Langmuir
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