CID 767
H2CO3
Carbonic acid
- H 2
- C 1
- O 3
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- IUPAC name
- carbonic acid
- Molar mass
- 62.0240(54) g/mol
- Atoms
- 6
- SMILES
- C(=O)(O)O
- InChIKey
- BVKZGUZCCUSVTD-UHFFFAOYSA-N
- PubChem CID
- 767
Rain, soda water and human blood each hold a little carbonic acid, made when dissolved carbon dioxide reacts with the water around it. Its molecule joins one carbon, two hydrogen and three oxygen atoms, 62.024 g/mol in all. The US National Oceanic and Atmospheric Administration (NOAA) calls it a weak acid that comes apart in water into a hydrogen ion and a bicarbonate ion. ChEBI, a database of small biological molecules, names it the conjugate acid of hydrogencarbonate, another name for bicarbonate: the acid that ion becomes when it gains a proton.
Only a sliver of the dissolved gas ever becomes the acid. Such a solution is mostly hydrated CO2, the gas loosely bound to the water around it, according to Stephen Lower’s Chem1 textbook. The acid itself cannot be isolated pure under ordinary conditions.
Structure and bonding
One carbon, three oxygens and two hydrogens make up carbonic acid. The carbon sits in the middle, bonded to all three oxygens, one by a double bond. Each hydrogen hangs from one of the other two oxygens, never from the carbon. Turned edge-on, all six atoms fall into one plane. In this computed model the angles around the carbon are uneven: about 125° between the double bond and each single C–O, about 110° between the two single ones.
Ball-and-stick shows the double bond as the shortest of the three, 1.22 Å in the model against 1.35 Å for each single C–O. That matches Chem1’s rule that multiply bonded atoms lie closer together than singly bonded ones. Stick drops the balls and keeps the flat frame. Space-filling packs the spheres tightly: three oxygens crowd round the carbon, and the hydrogens show only as small caps on two of them.
The model draws the neutral molecule, which is not what dissolved carbon dioxide mostly becomes. The small share that becomes carbonic acid splits into hydrogen ions and bicarbonate ions, HCO3−, and the viewer draws neither.
Where it turns up
Rain turns acidic on its way down. Falling drops take in carbon dioxide from the air, and part of it reacts to give carbonic acid. On Chem1’s account the same happens to all pure water left in contact with air. Freshly distilled water shows the same effect, its pH creeping downward as the gas dissolves from the air.
The tingle of soda water on your tongue is carbonic acid too. It forms where bubbles of carbon dioxide touch the mucous membranes, the moist lining of the mouth, as Chem1 describes it.
Chem1 traces the ocean’s large capacity for carbon dioxide to slightly alkaline water carrying it on to bicarbonate and carbonate ions. How far surface pH has fallen is set out on the carbon dioxide page, and what that means for shells on the calcium carbonate page.
Why it matters
ChEBI lists carbonic acid as a mouse metabolite, a substance the animal’s body chemistry produces, and human cells make it too. Every cell releases carbon dioxide as a by-product of its metabolism, and in water part of the gas reacts to form the acid. Converted to bicarbonate, it travels safely in the blood to the lungs. There carbonic acid loses water, and the carbon dioxide it gives up leaves in the breath. Carbonic acid that the body makes from food takes the same exit, most of it breathed out almost at once, Chem1 notes.
Blood is buffered, kept at a steady pH, while carbon dioxide from metabolism is added to it and then removed by the lungs. In Chem1’s account the carbonate system is the body’s main buffer, and at normal physiological pH it exists mostly as bicarbonate, not as the acid drawn in the model.
Properties
| Property | Value | Unit | Source |
|---|---|---|---|
| Molecular formula (Hill order) | CH2O3 | ||
| Molar mass | 62.0240(54) g/mol | g/mol | IUPAC/CIAAW 2024 |
| Hydrogen atoms | 2 | ||
| Carbon atoms | 1 | ||
| Oxygen atoms | 3 | ||
| Bonds | 5 | ||
| Single bonds | 4 | ||
| Double bonds | 1 | ||
| PubChem molecular weight | 62.025 g/mol | g/mol | PubChem |
Safety
Carbonic acid is a mild acid, formed from carbon dioxide and water in a nonhazardous reaction, on the description in PubChem’s carbon dioxide record. A single company’s notification to the European Chemicals Agency (ECHA) gives it the signal word Warning, calling it harmful if swallowed, inhaled or in contact with skin. The same notification lists skin irritation, serious eye irritation and possible respiratory irritation, all gathered in the PubChem Laboratory Chemical Safety Summary for carbonic acid.
Questions
Can you buy pure carbonic acid?
Not as a pure chemical. Under ordinary conditions the acid cannot be isolated on its own, and it gives up water to become carbon dioxide again. New Zealand's Environmental Protection Authority has not approved it as a chemical to be used by itself. Its salts are another matter: carbonates and hydrogen carbonates are the forms in which, according to MeSH, the acid exists.
Is carbonic acid a strong or weak acid?
Weak. In water it releases H+ and becomes the bicarbonate ion, HCO3−, in NOAA's description. As it is usually met, in a solution of carbon dioxide, Chem1 lists it with boric acid among the very weak acids. The figure usually quoted for its strength is a blend, measured on a solution that is mostly dissolved carbon dioxide, so the pure acid is considerably stronger than that figure suggests.
Is carbonated water the same as carbonic acid?
Not quite. Carbon dioxide dissolved in a drink stays mostly as the gas, loosely bound to the water around it in what Chem1 calls a hydrate. Only a very small fraction of that hydrate combines into H2CO3, so the drink holds far more dissolved gas than acid. The acid it does hold is a mild one, as PubChem's carbon dioxide record describes it.
Made of the same elements
- HCOOH Formic acid 5 atoms, 4 bonds.
- CH2O Formaldehyde 4 atoms, 3 bonds.
- H2C2O4 Oxalic acid 8 atoms, 7 bonds.
- C2H4O3 Glycolic acid 9 atoms, 8 bonds.
- CH3COOH Acetic acid 8 atoms, 7 bonds.
- CH3OH Methanol 6 atoms, 5 single bonds.
- CH3CHO Acetaldehyde 7 atoms, 6 bonds.
- C2H4O Ethylene oxide 7 atoms, 7 single bonds.
All 51 compounds made of hydrogen, carbon and oxygen
- C2H6O2 Ethylene glycol 10 atoms, 9 single bonds.
- C3H6O3 Lactic acid 12 atoms, 11 bonds.
- CH3OCH3 Dimethyl ether 9 atoms, 8 single bonds.
- C2H5OH Ethanol 9 atoms, 8 single bonds.
- C2H5COOH Propionic acid 11 atoms, 10 bonds.
- C3H6O Acetone 10 atoms, 9 bonds.
- C3H8O3 Glycerol 14 atoms, 13 single bonds.
- C4H6O5 Malic acid 15 atoms, 14 bonds.
- C3H8O2 Propylene glycol 13 atoms, 12 single bonds.
- C3H7OH 1-Propanol 12 atoms, 11 single bonds.
- C3H7COOH Butyric acid 14 atoms, 13 bonds.
- CH3COOC2H5 Ethyl acetate 14 atoms, 13 bonds.
- C3H8O Isopropyl alcohol 12 atoms, 11 single bonds.
- C7H6O3 Salicylic acid 16 atoms, 16 bonds.
- C4H6O6 Tartaric acid 16 atoms, 15 bonds.
- C6H5COOH Benzoic acid 15 atoms, 15 bonds.
- C4H8O Butanone 13 atoms, 12 bonds.
- C6H5OH Phenol 13 atoms, 13 bonds.
- C6H5CHO Benzaldehyde 14 atoms, 14 bonds.
- C4H9OH 1-Butanol 15 atoms, 14 single bonds.
- C2H5OC2H5 Diethyl ether 15 atoms, 14 single bonds.
- C8H8O3 Methyl salicylate 19 atoms, 19 bonds.
- C8H8O3 Vanillin 19 atoms, 19 bonds.
- C6H8O6 Ascorbic acid 20 atoms, 20 bonds.
- C9H8O4 Aspirin 21 atoms, 21 bonds.
- C6H8O7 Citric acid 21 atoms, 20 bonds.
- C6H12O6 Fructose 24 atoms, 24 single bonds.
- C6H12O6 Glucose 24 atoms, 24 single bonds.
- C14H14O3 Naproxen 31 atoms, 32 bonds.
- C15H16O2 Bisphenol A 33 atoms, 34 bonds.
- C13H18O2 Ibuprofen 33 atoms, 33 bonds.
- C10H20O Menthol 31 atoms, 31 single bonds.
- C20H14O4 Phenolphthalein 38 atoms, 41 bonds.
- C12H22O11 Lactose 45 atoms, 46 single bonds.
- C12H22O11 Sucrose 45 atoms, 46 single bonds.
- C18H24O2 Estradiol 44 atoms, 47 bonds.
- C19H28O2 Testosterone 49 atoms, 52 bonds.
- C16H32O2 Palmitic acid 50 atoms, 49 bonds.
- C21H30O2 Progesterone 53 atoms, 56 bonds.
- C21H30O5 Cortisol 56 atoms, 59 bonds.
- C18H34O2 Oleic acid 54 atoms, 53 bonds.
- C27H44O Cholecalciferol 72 atoms, 74 bonds.
- C27H46O Cholesterol 74 atoms, 77 bonds.
Sources
- PubChem CID 767, carbonic acid
- IUPAC/CIAAW, Abridged Standard Atomic Weights 2024
- PubChem Laboratory Chemical Safety Summary for carbonic acid (CID 767)
- Stephen Lower, Chem1 General Chemistry, §8.2.2B Solutions of Gaseous Solutes in Liquid Solvents (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §9.2 Molecules - Properties of Bonded Atoms (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §10.2 Aqueous Solutions - pH and Titrations (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §10.3 Acid-Base Reactions à la Brønsted (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §12 Solubility Equilibria (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §13.2 Strong Monoprotic Acids and Bases (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §13.4 Conjugate Pairs and Buffers (LibreTexts, CC BY 3.0)
- Stephen Lower, Chem1 General Chemistry, §13.6 Applications of Acid-Base Equilibria (LibreTexts, CC BY 3.0)
- NOAA Education, Ocean Acidification
- PubChem CID 280, carbon dioxide