Organic carbonic acids
Organic carbonic acids are a class of compounds that contain both carboxylic acid and carbonate functional groups. These molecules play significant roles in various chemical processes, particularly in biological systems where they facilitate the transport and regulation of bicarbonate ions (HCO??) within cells and tissues. Common examples include malonic acid, succinic acid, and oxaloacetic acid, which are essential intermediates in metabolic pathways such as the citric acid cycle.
These acids exhibit unique properties due to their dual nature, enabling them to act as proton donors or acceptors depending on environmental pH. Their ability to form salts with bases also makes them useful in various synthetic reactions. In industrial applications, organic carbonic acids find use in pharmaceuticals, food additives, and analytical reagents, where they are valued for their stability and reactivity.
Overall, the properties of organic carbonic acids make them valuable tools across multiple disciplines within chemistry and biology.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Carbonate, hydrogen(8CI,9CI) | 71-52-3 | CHO3 |
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Almagate | 66827-12-1 | CH11AlMg3O12 |
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Sevelamer Carbonate, Technical Grade | 845273-93-0 | C7H14ClNO4 |
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Erbium(III) carbonate hydrate | 22992-83-2 | CH4ErO4 |
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Neodymium carbonate | 38245-38-4 | C3H2Nd2O10 |
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Cerium(III) carbonate hydrate | 54451-25-1 | C3H2Ce2O10 |
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europium(iii) carbonate hydrate | 86546-99-8 | CH4EuO4 |
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Potassium carbonate | 584-08-7 | CK2O3 |
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Nickel(II) Carbonate Tetrahydroxide | 12607-70-4 | CHNiO4 |
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Ammonium Carbonate-15N | 402835-84-1 | CH8N2O3 |
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