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99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder

China Hangzhou Fuluo Biological Technology Co.,Ltd. certification
China Hangzhou Fuluo Biological Technology Co.,Ltd. certification
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99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder

99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder
99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder 99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder

Large Image :  99.86% Chemicals Pain Reliever Drug / Local Anesthetic Lidocaine HCL Powder

Product Details:
Place of Origin: WuHan
Brand Name: YuanCheng
Certification: ISQ9001
Model Number: lidocaine hcl
Payment & Shipping Terms:
Minimum Order Quantity: 10g
Price: bargaining
Packaging Details: Discreet packaging
Delivery Time: 4-7 working days
Payment Terms: T/T, Western Union, MoneyGram.Bitcoin
Supply Ability: 1200kg/month
Detailed Product Description
Brand: Yuancheng CAS: Lidocaine Hcl
Certificate: ISQ90001 Price: Bargaining
Packing: Discreet Packaging Appearance: White Crystalline Powder
High Light:

topical anesthetic agents


local anesthetics drugs

BP Standard Lidociane HCL Powder,99.86% Lidocaine HCL


Product Name: Lidocaine hydrochloride
CAS: 73-78-9
MF: C14H23ClN2O
MW: 270.8
EINECS: 200-803-8
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Research Chemical;Pharma materials
Mol File: 73-78-9.mol
Lidocaine hydrochloride Structure

Chemical Properties White to Off-White Solid
Usage Local anesthesic;Na+ channel blocker
Usage Anesthetic (local); antiarrhythmic (class IB). Long-acting, membrane stabilizing agent against ventricular arrhythmia. Originally developed as a local anesthetic.
Definition ChEBI: The anhydrous form of the hydrochloride salt of lidocaine.


Lidocaine hydrochloride for amide local anesthetics. After the absorption of blood or intravenous administration, there was biphasic excitatory and inhibitory effects on the central nervous system, and no precursor excited, blood concentration is low, analgesic and sleepiness, pain threshold increased; with the dose increase, enhancing effect or toxicity, have the anticonvulsant effect of inferior toxic blood concentration.

When the blood concentration of more than 5 mu g ml-1 convulsions may occur. The goods at low doses, can promote myocardial intracellular k+ outflow, reduce myocardial and self-discipline, has antiarrhythmic effect; in therapeutic doses, had no significant effect on the electrical activity of myocardial cells, the atrioventricular and myocardium contraction; blood drug concentration increased further, which can cause cardiac conduction velocity, atrioventricular block, inhibition of myocardial contractility and cardiac output decreased.


The goods after the injection, tissue distribution of fast and wide, can penetrate the blood-brain barrier and the placenta. The anesthesia of high strength, quick effect, dispersion force, from the local drug elimination takes about 2 hours, plus epinephrine can prolong the action time. Most of the first by the enzyme degradation of liver microsomes for local anesthesia is still used deethylase intermediate metabolite monoethyl glycinamide increased toxicity, xylene, followed by amide hydrolysis, excreted in the urine, about 10% in the base amount of discharge, a few appeared in bile.
Cardiac output decreased.



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