biological source
wood (pulp cellulose)
form
powder
autoignition temp.
698 °F
concentration
48.0-49.5%
extent of labeling
48-49.5% ethoxy content
refractive index
n20/D 1.47 (lit.)
viscosity
~45 cP, 5 % in toluene/ethanol 80:20(25 °C)(lit.)
density
1.14 g/mL at 25 °C (lit.)
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Application
Ethyl cellulose is generated by converting a variable number of hydroxyl groups on the repeating glucose units to ethyl ether groups. Ethylcellulose is used in the preparation of biostructures such as matrices, microspheres, microparticles, pellets and tablets for use in drug delivery.
Legal Information
Ethocel is a registered trademark of The Dow Chemical Company or an affiliated company of Dow
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Niklas Sandler et al.
Scientific reports, 4, 4020-4020 (2014-02-08)
The developments in printing technologies allow fabrication of micron-size nano-layered delivery systems to personal specifications. In this study we fabricated layered polymer structures for drug-delivery into a microfluidic channel and aimed to interferometrically assure their topography and adherence to each
Francisco Flores-Céspedes et al.
Journal of agricultural and food chemistry, 60(4), 1042-1051 (2012-01-10)
Imidacloprid, a systemic insecticide that has a water solubility of 610 mg L(-1), has been formulated in lignin-polyethylene glycol matrices by a melting process. This formulation was coated in a Wurster type fluidized-bed equipment using ethylcellulose and dibutyl sebacate. Imidacloprid
Yutaka Okuda et al.
International journal of pharmaceutics, 423(2), 351-359 (2011-12-06)
The aim of this study is to design a new orally disintegrating tablet (ODT) containing micronized ethylcellulose (MEC). The new ODT was prepared by physical mixing of rapidly disintegrating granules (RDGs) with MEC. To obtain RDGs, mannitol was spray-coated with
Ghulam Murtaza
Acta poloniae pharmaceutica, 69(1), 11-22 (2012-05-12)
Ethylcellulose (EC) based microencapsulated drug delivery systems are being extensively studied throughout the world for achieving extended drug release and protecting the core substance from degradation. The in vitro evaluation of EC microcapsules have elucidated that their particle characteristics are
Oguzhan Gunduz et al.
Pharmaceutical research, 30(1), 225-237 (2012-09-08)
To investigate a new microfluidic method for the continuous preparation of hollow-shell nanoparticles of a hydrophobic polymer and the simultaneous encapsulation within these of a hydrophilic active pharmaceutical ingredient. A specially designed and constructed microfluidic device which facilitates at a
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