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200697

Sigma-Aldrich

Ethyl cellulose

viscosity 22 cP, 5 % in toluene/ethanol 80:20(lit.), extent of labeling: 48% ethoxyl

Synonym(s):

Ethylcellulose

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12162002
NACRES:
NA.23

form

powder

Quality Level

autoignition temp.

698 °F

concentration

47.5-49.5%

extent of labeling

48% ethoxyl

refractive index

n20/D 1.47 (lit.)

viscosity

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

transition temp

softening point 155 °C

density

1.14 g/mL at 25 °C (lit.)

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General description

Ethyl cellulose is a non-toxic polysaccharide type gelator widely used in surface coatings and biomedical applications.

Application

Ethyl cellulose can be used:
  • To prepare oleogels for the ophthalmic delivery of hydrophilic drugs.
  • As a coating agent to synthesize flexible bioplastics for packaging applications.
  • To prepare CuO/Cu2O granules for thermochemical heat storage applications.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Anurag Verma et al.
Acta pharmaceutica (Zagreb, Croatia), 62(2), 237-250 (2012-07-04)
Chitosan has become a focus of major interest in recent years due to its excellent biocompatibility, biodegradability and non-toxicity. Although this material has already been extensively investigated in the design of different types of drug delivery systems, it is still
Daniela Traini et al.
International journal of pharmaceutics, 438(1-2), 150-159 (2012-09-12)
The potential of excipient coating to enhance aerosol performance of micronized drugs in carrier excipient-drug blends, used in dry powder inhalers, was investigated. Both EC (ethyl cellulose) and PVP (polyvinylpyrrolidone) were used as coating agents. Carriers were prepared via sieve
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
Kifayat Ullah Shah et al.
TheScientificWorldJournal, 2012, 842348-842348 (2012-06-01)
The design and fabrication of sustained/controlled release dosage forms, employing new excipients capable of extending/controlling the release of drugs from the dosage forms over prolonged periods, has worked well in achieving optimally enhanced therapeutic levels of the drugs. In this
Xin Li et al.
Die Pharmazie, 67(8), 695-700 (2012-09-11)
A novel osmotic pump tablet with ethyl cellulose (EC) and polyvinyl pyrrolidone (PVP) as the semipermeable membrane and isosorbide-5-mononitrate (5-ISMN) as the model drug was formulated in this study. Zero order release kinetics were attained by avoiding aging during storage.

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