CAS 6108-05-0 Local Anesthetic Drugs Lidocaine Hydrochloride Lidocaine HCL
Product Name: Linocaine hydrochloride
Melting point : 75-79℃
form : solid
color : white
White crystal, odorless, slightly bitter and taste. Easily soluble in water, ethanol and organic solvents, but insoluble in ether. Aqueous solution in acid, alkali case does not decompose, repeated little autoclave deterioration.
Surface anesthesia with 2% ~ 5% solution. Infiltration anesthesia with 0.25% ~ 0.5% solution. Conductive anesthesia with 2% lidocaine hydrochloride solution, each injection point, horse, cow 8 to 12 ml, sheep 3 to 4 ml. Epidural anesthesia 2% solution, horse, cow 8 to 12 ml, dogs and cats 0.22 ml per kilogram of body weight. Subcutaneous injection with 2% solution, the maximum amount of pigs, sheep 80 ml, horses, cattle 400 ml, dogs 25 ml, cat 8.5 ml.
Treatment of arrhythmia, intravenous injection: the first dose of 2 to 4 mg per kilogram of body weight dogs, followed by intravenous infusion of 25 to 75 micrograms per minute, cat first dose of 250 to 500 micrograms, followed by intravenous infusion of 20 micrograms per minute.
Lidocaine hydrochloride in the role of local anesthetic amide. For local anesthetics and anti-arrhythmic drugs. Mainly used:
(1) Infiltration anesthesia, epidural anesthesia, topical anesthesia (including mucosal anesthesia for thoracoscopy or peritoneal surgery), and nerve block.
(2) Treatment of premature ventricular contractions and ventricular tachycardia after AMI, and digitalis poisoning, cardiac surgery, cardiac catheterization-induced ventricular arrhythmias, but are generally ineffective for supraventricular arrhythmias.
Lidocaine hydrochloride has the characteristics of strong penetration, strong dissemination, rapid onset of action, twice the anesthetic potency and procaine, and a toxicity of 1. 5 minutes after treatment can occur anesthesia, anesthesia for 1 to 1.5 hours, 50% longer than procaine. After absorption can inhibit the central nervous system, and can inhibit ventricular autonomy, shortening refractory period, can be used to control ventricular tachycardia, premature ventricular contractions, ventricular tachycardia and ventricular fibrillation and other arrhythmia symptoms. Right heart disease or cardiac arrhythmia caused by cardiac glycosides are effective, supraventricular tachycardia is not effective. This product is fast, short duration, oral invalid, often as intravenous injection.
Our other main products:
|Melanotan II (MT-2)
|p-aminobenzene sulfonic acid, (Sulfanilic acid)
|sodium dimethyl dithiocarbamate
|Gamma butyrolactone (GBL)
|1, 2 - adipic alcohol
|Lidocaine hydrochloride(Lidocaine HCL)
|Benzyl alcohol (BA)
|IGF 1 LR3
|TB500 (5 mg)
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