Trimecaine

Names
IUPAC name N2,N2-Diethyl-N1-(2,4,6-trimethylphenyl)glycinamide
Systematic IUPAC name 2-(Diethylamino)-N-(2,4,6-trimethylphenyl)acetamide
Other names N2,N2-diethyl-N-mesitylglycinamide
Identifiers
CAS Number	616-68-2 Y
3D model (JSmol)	Interactive image
ChemSpider	11533
ECHA InfoCard	100.009.535
EC Number	210-487-3
KEGG	D08640
MeSH	D014288
PubChem CID	12028
UNII	IN1233R0JO Y
CompTox Dashboard (EPA)	DTXSID6048410
InChI InChI=1S/C15H24N2O/c1-6-17(7-2)10-14(18)16-15-12(4)8-11(3)9-13(15)5/h8-9H,6-7,10H2,1-5H3,(H,16,18) Key: GOZBHBFUQHMKQB-UHFFFAOYSA-N
SMILES CCN(CC)CC(=O)NC1=C(C=C(C=C1C)C)C
Properties
Chemical formula	C15H24N2O
Molar mass	248.36386
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Trimecaine (systematic name (2,4,6-trimethylphenylcarbamoylmethyl)diethylammonium chloride, chemical formula C₁₅H₂₅ClN₂O) is an organic compound used as a local anesthetic and cardial antiarrhythmic. It is white crystalline powder readily soluble in water and ethanol.^[1] It is an active ingredient in products available under trademarks Mesdicain, Mesocain, Mesokain and others.^[2]

Trimecaine is probably a Czech discovery (in light of complex pharmacological and clinical evaluation and practical deployment) although its preparation was published by Löfgren in 1946.^[2]

Like other local anesthetics belonging in the amide group trimecaine decreases the cell membrane permeability, causes depolarization and shortens the action potential.^[3] Anesthetic effect starts within 15 minutes and remains 60–90 minutes. Its biological half-life is ca. 90 minutes. 10% of trimecaine is excreted unchanged (90% as its metabolites). It passes through the hematoencephalic and placental barriers.^[4]

Trimecaine has two main application fields. The first one is local anesthesia (topical, infiltrational, topical mucosal and inhalational, spinal and Bier's intravenous). It is used in concentrations 0.4 up to 4%, in some cases (e.g. in stomatology) in mixtures with adrenaline. The other field is prophylaxis and therapy of ventriculous arrhythmia on myocardial infarction and in cardiosurgery. It is used also for prophylaxis of sympathetic reaction during tracheal intubations.^[3][4]

Trimecaine must not be used at hypersensitivity on amide anesthetics, hypervolemia, hypotension, cardial conduction defects, asystole, cardiogenic shock and malignant hyperthermia in anamnesis.^[3][4]

Rarely allergic reactions may occur (from dermal or mucosal symptoms to anaphylactic shock). At overdosing a toxical reaction arises - excitation, agitation, dishevelment, visual defects, buzzing in ears, muscle thrill to tremor, in more severe cases somnolence, hyporeflexia, breathing defects to apnea, convulsions.^[3][4]