Citric acid
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| Citric acid | |
|---|---|
| IUPAC name | 2-hydroxypropane-1,2,3-tricarboxylic acid |
| Other names | 3-carboxy-3-hydroxypentanedioic acid |
| Identifiers | |
| CAS number | |
| PubChem | |
| DrugBank | DB04272 |
| KEGG | D00037 |
| ChEBI | CHEBI:30769 |
| SMILES | C(C(=O)O)C(CC(=O)O)(C(=O)O)O |
| Properties | |
| Molecular formula | C6H8O7 |
| Molar mass | 192.124 g/mol (anhydrous) 210.14 g/mol (monohydrate) |
| Appearance | crystalline white solid |
| Density | 1.665 g/cm3(1.5g/cm3 for monohydrate) |
| Melting point |
153 °C, 426 K, 307 °F |
| Boiling point |
175 °C, 448 K, 347 °F (decomposes) |
| Solubility in water | 73 g/100 ml (20 °C) |
| Acidity (pKa) | pKa1 = 3.09 pKa2 = 4.75 pKa3 = 5.41 [1] |
| Hazards | |
| Main hazards | skin and eye irritant |
| Related compounds | |
| Related compounds | sodium citrate, calcium citrate |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Citric acid is a weak organic acid. It can be found in citrus fruits ( like oranges). It acts like a preservative. It is also used to add a sour (acidic) taste to foods and soft drinks. In the European Union it is known as E 330, as a food additive.
Carl Wilhelm Scheele was the first who could extract citric acid from lemons, in 1782. The substance was probably known to alchemists, perhaps with a different name. The Arabian alchemist Geber is said to have discovered citric acid in the 9th century. Citric Acid contains 6 Carbon atoms, 8 Hydrogen atoms and 7 Oxygen atoms. Its chemical formula is C6H8O7.
[change] Main uses
- As a water softener
- It is often used in detergents, to avoid the smell of acid, esp. Acetic acid
- As a preserving agent
- Citric acid and its salts prevent blood clotting. Blood donations are kept liquid using citric acid.
[change] References
- ↑ Dawson, R. M. C.; et al. (1959). Data for Biochemical Research. Oxford: Clarendon Press.