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PRODUCTION
Prepared by agitating alkali cellulose with ethyl chloride et
60C for several hours.
STRUCTURE:
NONPROPRIETARY NAMES
BP: Ethylcellulose
PhEur: Ethylcellulosum
USPNF: Ethylcellulose
SYNONYMS
Aquacoat ECD;
Aqualon; E462;
Ethocel;
Surelease
FUNCTIONAL CATEGORY:
Coating agent; flavoring fixative; tablet binder; tablet filler;
viscosity-increasing agent.
HISTORY
SOLUBILITY:
Insoluble in water, glycerin and propylene glycol and soluble
in some organic solvents such as alcohol, ether, ketone, ester,
aromatic hydrocarbon.
STABLITY:
Stable against light, heat, oxygen, wetness and alkali, dilute
acid and salting liquid.
It undergoes oxidative degradation in the presence of
sunlight or UV light at elevated temperatures. Use of
antioxidant and chemical additives that absorb light in the
230–340nm range can prevent it.
COMPATIBLE WITH:
Many celluloses, resin and nearly all plasticizers.
INCOMPATIBLE WITH:
Incompatible with paraffin wax and microcrystalline wax.
MOISTURE CONTENT:
It absorbs very little water from humid air or during
immersion, and that small amount evaporates readily
OTHER PROPERTIES:
Density-0.4 g/cm3
Specific gravity- 1.07- 1.18,
Glass Transition Temperature-129–1338C(26)
Non flammable, Flexible
ETHYL CELLULOSE PLASTICS
Thermoplastics,
Toughest,
Lightest ,
Ease of molding,
light weight,
good dielectric strength,
Retention of flexibility over a wide range of temp.
SAFETY
Nontoxic, Non allergenic and Nonirritating material.
Because ethyl cellulose is not metabolized
it is not recommended for parenteral products; parenteral
use may be harmful to the kidneys.
REGULATORY STATUS
GRAS listed. Accepted for use as a food additive in Europe.
Included in the FDA Inactive Ingredients Guide (oral
capsules, suspensions and tablets; topical emulsions and
vaginal preparations).
Included in non-parenteral medicines licensed in
Europe. Included in the Canadian List of Acceptable Non-
medicinal Ingredients.