
|
Prepared at the 17th JECFA (1973), published in FNP 4 (1978) and in FNP 52 (1992) |
|
SYNONYMS |
INS No. 404 |
DEFINITION |
Calcium Alginate, the calcium salt of alginic acid, is a colloidal substance. The alginic acid is a linear high-polymer consisting mainly of ß-(1→4) linked D-mannuronic acid in the pyranose ring form, with part of the mannuronic acid replaced by L-guluronic acid. |
C.A.S. number |
9005-35-0 |
Chemical formula |
(C6 H7 Ca1/2 O6)n |
Structural formula |
![]()
![]()
|
Formula weight |
Structural unit: 195.16 (theoretical), 219 (actual average) Macromolecule: 32,000 - 250,000 |
Assay |
Not less than 18.0% and not more than 21.0% of carbon dioxide (CO2), equivalent to not less than 89.6% and not more than 104.5% of calcium alginate (C6H7Ca1/2 O6)n. |
DESCRIPTION |
White to yellowish brown filamentous, grainy, granular and powdered forms |
FUNCTIONAL USES |
Stabilizer and thickener. |
CHARACTERISTICS | |
IDENTIFICATION | |
Solubility |
Insoluble in water and ether; slightly soluble in ethanol; slowly soluble in solutions of sodium polyphosphate, sodium carbonate, and substances that combine with the calcium. |
Specific rotation |
Clarify a 0.5% solution of the sample in sodium hydroxide TS with kieselguhr, and determine the rotation in a 20-cm tube. The specific rotation is not less than -0.8o at 20o. |
Precipitate formation with calcium chloride |
To a 0.5% solution of the sample in sodium hydroxide TS add one-fifth of its volume of a 2.5% solution of calcium chloride. A voluminous, gelatinous precipitate is formed. This test distinguishes ammonium alginate from gum arabic, sodium carboxymethyl cellulose, carrageenan, gelatin, gum ghatti, karaya gum, carob bean gum, methyl cellulose and tragacanth gum. |
Precipitate formation with ammonium sulfate |
To a 0.5% solution of the sample in sodium hydroxide TS add one-half of its volume of a saturated solution of ammonium sulfate. No precipitate is formed. This test distinguishes ammonium alginate from agar, sodium carboxymethyl cellulose, carrageenan, de-esterified pectin, gelatin, carob bean gum, methyl cellulose and starch. |
Colour reaction |
Passes test Moisten 1-5 mg of the sample with water, and add 1 ml of acid ferric sulfate TS. Within 5 min, a cherry-red colour develops that finally becomes deep purple. |
Test for calcium |
Passes test Dissolve the sulfated ash of the sample in dilute acetic acid TS and filter. Treat the filtrate with ammonium oxalate TS. The white precipitate formed is soluble in hydrochloric acid. |
PURITY | |
Loss on drying |
Not more than 15% (105o, 4 h) |
Phosphate |
Not detectable To an 0.5% aqueous solution of the sample add one-fifth of its volume of 4 N nitric acid and 1 volume of ammonium molybdate TS and warm. No yellow precipitate should be formed. |
Total ash |
Not less than 13% and not more than 24% on the dried basis |
Arsenic |
Not more than 3 % mg/kg (Method II) |
Lead |
Not more than 10 mg/kg Prepare a sample solution as directed for organic compounds in the Limit Test, using 10 µg of lead ion (Pb) in the control |
Heavy metals |
Not more than 40 mg/kg Test 0.5 g of the sample as directed under the Limit Test (Method II) |
METHOD OF ASSAY |
Decarboxylation methodProceed as directed under Carbon Dioxide Determination by Decarboxylation in the General Methods. Each ml of 0.25 N sodium hydroxide consumed is equivalent to 5.5 mg of carbon dioxde (CO2) or 27.38 mg of calcium alginate (equivalent weight 219.00).
Gravimetric methodDissolve 0.500 g of the sample in 10 ml of sodium hydroxide TS, add 90 ml of water, and filter if necessary. Add 15 ml of 4 N hydrochloric acid and 100 ml of 90% v/v ethanol. Allow this mixture to stand for 2 h, decant the supernatant liquid as far as possible, and centrifuge. Decant the liquid and replace it by 90% v/v ethanol. Mix well, centrifuge and decant again. This washing is repeated until the hydrochloric acid is removed. Then transfer the precipitate by mean of 90% v/v ethanol to a fine glass filter, wash with dry acetone, place the filter in a vacuum desiccator, and dry to constant weight at 100o.
Calculate the percent purity of the sample by the formula:
% Purity = (200 x F x W ) / % dry substance in sample x 100
in which F is a conversion factor specified as 1.108 and W is the weight (in grams) of the dried precipitate. |