TRIACETIN-三乙酸甘油酯(甘油三乙酸酯)
TRIACETIN
Prepared at the 46th JECFA (1996), published in FNP 52 Add 4 (1996)
superseding specifications prepared at the 19th JECFA (1975), published in
NMRS 55B (1976) and in FNP 52 (1992). Metals and arsenic specifications
revised at the 63rd JECFA...
TRIACETIN
Prepared at the 46th JECFA (1996), published in FNP 52 Add 4 (1996)
superseding specifications prepared at the 19th JECFA (1975), published in
NMRS 55B (1976) and in FNP 52 (1992). Metals and arsenic specifications
revised at the 63rd JECFA (2004). An ADI 'not specified' was established at
the 19th JECFA (1975)
SYNONYMS Glyceryl triacetate, INS No. 1518
DEFINITION
Chemical names Glyceryl triacetate
C.A.S. number 102-76-1
Chemical formula C9H14O6
Structural formula
Formula weight 218.21
Assay Not less than 98.5% on the anhydrous basis
DESCRIPTION Colourless, somewhat oily liquid having a slight, fatty odour
FUNCTIONAL USES Humectant, solvent
CHARACTERISTICS
IDENTIFICATION
Solubility (Vol. 4)
Sparingly soluble in water, soluble in ethanol
Test for glycerol Heat a few drops in a test tube with about 0.5 g of potassium bisulfate.
Pungent vapours of acrolein are evolved
Test for acetate (Vol. 4)
Passes test
To be performed on the solution resulting from the assay
PURITY
Water (Vol. 4)
Not more than 1.0% (Karl Fischer Method)
Refractive index (Vol. 4)
1.429 - 1.431 at 25o
Specific gravity (Vol. 4)
d (25, 25): 1.154 - 1.158
Distillation range (Vol. 4)
258 - 270o
Sulfated ash (Vol. 4)
Not more than 0.02%
Test 5 g of the sample (Method II)
Acidity Accurately weigh a sample of 25 g, dilute with 50 ml of neutralized ethanol,
and add 5 drops of phenolphthalein TS. Not more than 1 ml of 0.02N
sodium hydroxide is required to produce a pink colour.
Unsaturated compounds To 10 ml of the sample in a glass-stoppered tube add dropwise a 1 in 100
solution of bromine in carbon tetrachloride until a permanent yellow colour is
produced. No turbidity or precipitate appears after 18 h in the dark.
Lead (Vol. 4)
Not more than 2 mg/kg
Determine using an atomic absorption technique appropriate to the
specified level. The selection of sample size and method of sample
preparation may be based on the principles of the method described in
Volume 4, “Instrumental Methods.”
METHOD OF
ASSAY
Transfer about 1 g of the sample, accurately weighed, into a suitable
pressure bottle, add 25 ml of 1N potassium hydroxide and 15 ml of
isopropanol, stopper the bottle, and wrap securely in a canvas bag. Heat in
a water bath maintained at 98±2o for 1 h, allowing the water in the bath to
just cover the liquid in the bottle. Remove the bottle from the bath, cool in air
to room temperature, then loosen the bag, uncap the bottle to release any
pressure, and remove the bag. Add 6 to 8 drops of phenolphthalein TS, and
titrate the excess alkali with 0.5N sulfuric acid just to the disappearance of
the pink colour. Perform a blank determination. Each ml of 0.5N sulfuric acid
is equivalent to 36.37 mg of C9H14O6.
TRIACETIN
SYNONYMS
DEFINITION
Chemical names
C.A.S. number
Chemical formula
Structural formula
Formula weight
Assay
DESCRIPTION
FUNCTIONAL USES
CHARACTERISTICS
IDENTIFICATION
Test for glycerol
PURITY
Acidity
Unsaturated compounds
METHOD OF ASSAY
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