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433837

Sigma-Aldrich

Ethyl cellulose

viscosity 46 cP, 5 % in toluene/ethanol 80:20(lit.), extent of labeling: 48% ethoxyl

Synonym(s):

Cellulose ethylate

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About This Item

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

description

water vapor transmission 890 g/m2/24hrs 3-mil. film (ASTM E96-66,E)

form

powder

autoignition temp.

698 °F

hardness

52-61 (Sward, 3-mil. film)

concentration

48.0-49.5%

extent of labeling

48% ethoxyl
2.25-2.58 mol ethyl per mol cellulose (D.S.)

refractive index

n20/D 1.47 (lit.)

viscosity

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

transition temp

Tg 120-124 °C

solubility

esters, aromatic hydrocarbons, alcohols and ketones: soluble

density

1.14 g/mL at 25 °C (lit.)

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Application

Film-former in coatings, hot-melt adhesives and transfer inks and as a plastic coating for a variety of substrates.

Features and Benefits

Produces transparent films, unaffected by visible and UV light. Flexible over a wide temperature range (70 to 150 °C), exhibits low flammability and can be made flame-retardant. Compatible with plasticizers and modifiers to improve adhesion, gloss, hardness and water resistance.

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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Li-Ya Huang et al.
International journal of pharmaceutics, 436(1-2), 88-96 (2012-07-14)
A drug-loaded nanofiber mesh which could achieve time-engineeringed biphasic release was fabricated through sequential electrospinning. The drug to polymer ratio of each single mesh was allocated and designed before the tri-layered meshes were created. The resultant meshes had the following
H V Adikane et al.
Applied biochemistry and biotechnology, 169(3), 1026-1038 (2013-01-09)
The chemical modification of developed ethyl cellulose-based membrane was carried out to make it suitable for bioseparation. The different reagents were used for the modification of membrane to couple protein A (PA) to study the purification of immunoglobulin G (IgG)
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
N Suwannateep et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 82(3), 485-490 (2012-09-08)
The phytochemical curcumin possesses antioxidant activity; however, it becomes unstable after being exposed to light or heat or loses activity during storage. This is especially important when curcumin is applied to the skin within a cosmetic or pharmaceutical formulation, since
Syed Umer Jan et al.
Pakistan journal of pharmaceutical sciences, 25(4), 751-756 (2012-09-27)
The aim and objective of the present study was to formulate and evaluate controlled release polymeric tablets of ibuprofen with determinations of formulation factors using various grades and types of polymer ethocel i.e. ethocel standard 10P; 10FP, 100P and100FP for
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