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Prepared at the 39th JECFA (1992), published in FNP 52 Add 1 (1992) superseding specifications published in the Compendium of Food Additive Specifications (1992) |
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SYNONYMS |
INS No. 401 |
DEFINITION |
Sodium alginate is the sodium salt of alginic acid, is a hydrophilic, colloidal substance. |
C.A.S. number |
9005-38-3 |
Chemical formula |
(C6 H7 NaO6)n |
Structural formula |
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Formula weight |
Structural unit : 198.11 (theoretical), 222 (actual average) Macromolecule : 32,000 - 250,000 (typical average) |
Assay |
Yields, on the dried basis, not less than 18.0% and not more than 21.0% of carbon dioxide (CO2), equivalent to not less than 90.8% and not more than 106.0% of sodium alginate (C6H7 NaO6)n. |
DESCRIPTION |
Occurs as white to yellowish brown filamentous, grainy, granular or powdered forms |
FUNCTIONAL USES |
Stabilizer, thickener |
CHARACTERISTICS | |
IDENTIFICATION | |
Solubility |
Dissolves slowly in water, forming a viscous solution; insoluble in ethanol, ether and chloroform |
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 Dissolve as completely as possible 0.01 g of the sample by shaking with 0.15 ml of 0.1 N sodium hydroxide and add 1 ml of acid ferric sulfate TS. Within 5 min, a cherry-red colour develops that finally becomes deep purple. |
Test for sodium |
Passes test Dissolve the sulfated ash of the sample in dilute acetic acid TS and filter. Add to the filtrate uranyl zinc acetate TS. A yellow, crystalline precipitate is formed within a few minutes. |
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. |
Water-insoluble matter |
Not more than 1% on the dried basis Disperse 2 g of the sample, weighed to the nearest 0.1 mg, in 800 ml of water in a 2,000-ml flask. Neutralize to pH 7 with sodium hydroxide TS and then add 3 ml in excess. Cover the flask, heat to boiling, and boil for 1 h with frequent stirring. Filter while hot through a tared Gooch crucible provided with a glass fibre filter (2.4-cm, No. 934AH, Reeve Angel & Co., Clifton, N.Y., or equivalent filter). If slow filtration is caused by high viscosity of the sample solution, boil until the viscosity is reduced enough to permit filtration. Wash the crucible thoroughly with hot water, dry the crucible and its contents at 105o for 1 h, cool and weigh. Calculate as percentage of the dry weight. |
Total ash |
Not less than 18% and not more than 27% on the dried basis |
Arsenic |
Not more than 3 mg/kg (Method II) |
Lead |
Not more than 10 mg/kg |
Heavy metals |
Not more than 40 mg/kg Test 0.5 g of the sample as directed in the Limit Test (Method II) |
METHOD OF ASSAY |
Proceed as directed under Carbon Dioxide Determination by Decarboxylation. Each ml of 0.25 N sodium hydroxide consumed is equivalent to 5.5 mg of carbon dioxide (CO2) or 27.75 mg of sodium alginate (equivalent weight 222). |