Ascorbic Acid


Ascorbic acid occurs as a white to light-yellow-colored, nonhygroscopic, odorless, crystalline powder or colorless crystals with a sharp, acidic taste. It gradually darkens in color upon exposure to light.

Nonproprietary Names

BP: Ascorbic Acid
JP: Ascorbic Acid
PhEur: Ascorbic Acid
USP: Ascorbic Acid
Acidum ascorbicum; C-97; cevitamic acid; 2,3-didehydro-L-threohexono- 1,4-lactone; E300; 3-oxo-L-gulofuranolactone, enol form; vitamin C.
Synonyms

Acidum ascorbicum; C-97; cevitamic acid; 2,3-didehydro-L-threohexono- 1,4-lactone; E300; 3-oxo-L-gulofuranolactone, enol form; vitamin C.

Chemical Name and CAS Registry Number

L-(รพ)-Ascorbic acid [50-81-7]
Empirical Formula and Molecular Weight
C6H8O6 176.13
Functional Category
Antioxidant; therapeutic agent.

Applications in Pharmaceutical Formulation or Technology

Ascorbic acid is used as an antioxidant in aqueous pharmaceutical formulations at a concentration of 0.01–0.1% w/v. Ascorbic acid has been used to adjust the pH of solutions for injection, and as an adjunct for oral liquids. It is also widely used in foods as an antioxidant. Ascorbic acid has also proven useful as a stabilizing agent in mixed micelles containing tetrazepam.

Typical Properties

Acidity/alkalinity: pH = 2.1–2.6 (5% w/v aqueous solution)
Density (bulk): 0.7–0.9 g/cm3 for crystalline material; 0.5–0.7 g/cm3 for powder.
Density (particle): 1.65 g/cm3
Density (tapped): 1.0–1.2 g/cm3 for crystalline material; 0.9–1.1 g/cm3 for powder.
Density (true): 1.688 g/cm3
Dissociation constant: pKa1 = 4.17; pKa2 = 11.57.
Melting point: 1908°C (with decomposition)
Moisture content: 0.1% w/w

Method of Manufacture

Ascorbic acid is prepared synthetically or extracted from various vegetable sources in which it occurs naturally, such as rose hips, blackcurrants, the juice of citrus fruits, and the ripe fruit of Capsicum annuum L. A common synthetic procedure involves the hydrogenation of D-glucose to D-sorbitol, followed by oxidation using Acetobacter suboxydans to form L-sorbose. A carboxyl group is then added at C1 by air oxidation of the diacetone derivative of Lsorbose and the resulting diacetone-2-keto-L-gulonic acid is converted to L-ascorbic acid by heating with hydrochloric acid.




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