Anodyne

Lidocaine
Lidocaine
Salts
[]
Lidocaine tosylate
Lidocaine tosylate
Lidocaine hydrochloride
Lidocaine hydrochloride
Lidocaine carbonate
Lidocaine carbonate
Lidocaine bicarbonate
Lidocaine bicarbonate
Lidocaine iminodiacetic acid
Lidocaine iminodiacetic acid
Lidocaine maleate
Lidocaine maleate
Lidocaine sulfate
Lidocaine sulfate
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC14H22N2O
Molecular mass234.34 g/mol
AppearanceNeedles from benzene or alcohol
OdorCharacteristic odor
Predicted LogP2.3
Melting point68 °C
Boiling point159-160 °C at 2.00E+00 mm Hg
DecompositionWhen heated to decomposition it emits toxic fumes of /nitrogen oxides/.
Solubility>35.2 [ug/mL] (The mean of the results at pH 7.4)
Chiralityachiral
Identifiers
[]
IUPAC name2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide
SMILESCCN(CC)CC(=O)NC1=C(C=CC=C1C)C
InChIInChI=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)
InChIKeyNNJVILVZKWQKPM-UHFFFAOYSA-N
Dosing

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.

Stereochemistry

Lidocaine is a achiral mixture

See also