Bluedark| Lidocaine | |
|---|---|
 |
| Salts [] | |
|---|---|
| Lidocaine tosylate | |
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| Lidocaine hydrochloride | |
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| Lidocaine carbonate | |
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| Lidocaine bicarbonate | |
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| Lidocaine iminodiacetic acid | |
| |
| Lidocaine maleate | |
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| Lidocaine sulfate | |
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| Molecular structure via molpic | |
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| |
| Molecular formula | C14H22N2O |
|---|---|
| Molecular mass | 234.34 g/mol |
| Appearance | Needles from benzene or alcohol |
| Odor | Characteristic odor |
| Predicted LogP | 2.3 |
| Melting point | 68 °C |
| Boiling point | 159-160 °C at 2.00E+00 mm Hg |
| Decomposition | When heated to decomposition it emits toxic fumes of /nitrogen oxides/. |
| Solubility | >35.2 [ug/mL] (The mean of the results at pH 7.4) |
| Chirality | achiral |
| Identifiers [] | |
|---|---|
| IUPAC name | 2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide |
| SMILES | CCN(CC)CC(=O)NC1=C(C=CC=C1C)C |
| InChI | InChI=1S/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17) |
| InChIKey | NNJVILVZKWQKPM-UHFFFAOYSA-N |
Lidocaine
Lidocaine (also known as Lignocaine, 2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide, Xylocaine, Lidoderm, Duncaine, Esracaine, Xylestesin, Alphacaine, Cappicaine or Gravocain)
Chemistry
Lidocaine is typically found in the form of its tosylate, hydrochloride, carbonate, bicarbonate, iminodiacetic acid, maleate and sulfate salts.