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200654

Ethyl cellulose

viscosity 300 cP, 5 % in toluene/ethanol 80:20(lit.), extent of labeling: 48% ethoxyl

Synonym(s):

Ethylcellulose, Cellulose & cellulose derivatives

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About This Item

CAS Number:
9004-57-3
UNSPSC Code:
12162002
NACRES:
NA.23
MDL number:
MFCD00131037
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autoignition temp.

698 °F

Quality Level

100

concentration

48.0-49.5%

extent of labeling

48% ethoxyl

refractive index

n20/D 1.47 (lit.)

viscosity

300 cP, 5 % in toluene/ethanol 80:20(lit.)

transition temp

softening point 157 °C

density

1.14 g/mL at 25 °C (lit.)

SMILES string

O1[C@H](C(C(C(C1COCC)OCC)OCC)OCC)O[C@@H]2C(OC(C(C2OCC)OCC)OCC)COCC

InChI

1S/C28H54O11/c1-9-29-17-19-21(31-11-3)23(32-12-4)26(35-15-7)28(38-19)39-22-20(18-30-10-2)37-27(36-16-8)25(34-14-6)24(22)33-13-5/h19-28H,9-18H2,1-8H3/t19?,20?,21?,22-,23?,24?,25?,26?,27?,28+/m1/s1

InChI key

MINRZDZESGXKDM-OLIDUAMRSA-N

General description

Ethyl cellulose (EC) is a non-toxic, biocompatible, and hydrophobic polymer used for the sustained release preparation of pharmaceutical products.

Application

Ethyl cellulose can be used to prepare polymer coatings for various applications. For example, it is used to encapsulate salt hydrates for low-temperature heat storage applications.

It can be used as an efficient carrier for multiparticulate sustained drug delivery. For example, it can be used to develop polymeric microspheres for the controlled release of Ivabradine HCL (IBH).

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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV6652
MKCR1028
MKCS0410
MKCQ3889
MKCL1365

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Dace Gao et al.
Nanoscale horizons, 5(4), 730-738 (2020-02-18)
The design and construction of 3D architectures enabled by stimuli-responsive soft materials can yield novel functionalities for next generation soft-bodied actuating devices. Apart from additive manufacturing processes, origami inspired technology offers an alternative approach to fabricate 3D actuators from planar
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
Tetsuya Ozeki et al.
Biological & pharmaceutical bulletin, 35(11), 1926-1931 (2012-11-06)
Production of drug nanoparticles is an effective strategy to enhance solubility and oral absorption of water-insoluble drugs. The handling of drug nanoparticles has been an important issue in drug formulation because nanoparticles easily aggregate each other and redispersion of these
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