Lidocaine hydrochloride (73-78-9)

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  5 mg
  $140.00

  50 mg
  $1120.00

Most-cited Publications

• Inactivation of Hippocampus or Caudate Nucleus with Lidocaine Differentially Affects Expression of Place and Response Learning (Neurobiology of Learning and Memory, 1996)
• AMIODARONE AS COMPARED WITH LIDOCAINE FOR SHOCK-RESISTANT VENTRICULAR FIBRILLATION (The New England Journal of Medicine, 2002)
• Lidocaine block of cardiac sodium channels. (The Journal of General Physiology, 1983)
• The inhibition of sodium currents in myelinated nerve by quaternary derivatives of lidocaine. (The Journal of General Physiology, 1973)
• Both intravenous lidocaine and morphine reduce the pain of postherpetic neuralgia (Neurology, 1991)
• Formalin-evoked activity in identified primary afferent fibers: systemic lidocaine suppresses phase-2 activity (Pain, 1996)

Areas of Application

Safety

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Trends

Alternate Names

• Lidocaine
• Xylocaine
• Lignocaine
• Octocaine
• Lidocaine Hydrocarbonate
• Xyloneural
• 2-2EtN-2MePhAcN
• Dalcaine
• Xylocitin
• Lidocaine Sulfate (1:1)
• Lidocaine Monoacetate
• Lidocaine Carbonate
• 2-(Diethylamino)-N-(2,6-Dimethylphenyl)Acetamide
• Lidocaine Monohydrochloride, Monohydrate
• Lidocaine Monohydrochloride
• Lidocaine Carbonate (2:1)
• Xylesthesin
• SMILES
  CCN(CC)CC(=O)NC1=C(C=CC=C1C)C.Cl
• InChIKey
  IYBQHJMYDGVZRY-UHFFFAOYSA-N

External Links

• Pubchem - Lidocaine hydrochloride
• Wikipedia - lidocaine hydrochloride anhydrous

Synthesis

Ethylboronic acid  +  Monoethylglycinexylidide (Chan-Lam coupling reaction)

Acetyl chloride, (diethylamino)-  +  2,6-Dimethylaniline (Schotten-Baumann amide from acid)

Synthesis of Lidocaine hydrochloride ›

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Lidocaine hydrochloride

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