CAS 137-58-6 Lidocaine High Quality and Best Deivery

【Quality】 99.8% High purity
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CAS 137-58-6 Lidocaine High Quality and Best Deivery
Product Description
Product Name Lidocaine
Synonyms 2-(Diethylamino)-2′,6′-acetoxylidide;2-(diethylamino)-2’,6’-acetoxylidide;2-(diethylamino)-n-(2,6-dimethylphenyl)-acetamid;2′,6′-AcetoChemicalbookxylidide,2-(diethylamino)-;6’-acetoxylidide,2-(diethylamino)-2;Acetamide,2-(diethylamino)-N-(2,6-dimethylphenyl)-;Ligoncaine;Maricaine
CAS NO 137-58-6
Molecular Formula C14H22N2O
Molecular Weight 234.34
EINECS 205-302-8
Melting Point 66-69°C
Boiling Point bp4 180-182°; bp2 159-160°
Flash Point 9
Density 0.9944 (rough estimate)
Assay 99%
Grade Pharmaceutical Grade
Solubility Practically insoluble in water
Appearance White to slightly yellow powder
Storage Store at RT
Payment Western union, Bitcoin, XMR, USDT, TT
Delivery By sea, by air, all express modes (EMS,UPS,DHL,TNT,Fedex), 3-5 days after payment
Shipping adress Provide your valid and correct destination address info with post office code, phone number and consignee
Package Choose the most appropriate way according to quantity and safety degree
CAS 137-58-6 Usage

Lidocaine is an amide local anesthetic. Widely used in surface anesthesia, infiltration anesthesia, conduction anesthesia and epidural anesthesia

General description

Lidocaine is a local anesthetic and an effective antiarrhythmia agent. It occurs as solutions of crystalline colorless solid for injections, that has a short half-life within plasma.

Biochem/physiol Actions

Lidocaine, a neuroprotective agent, mediates blockage of sodium (Na+) channels.It prevents the influx of sodium ions leading to depolarization of sodium channels and metabolically inactivated in liver. Lidocaine has positive effect on cerebral ischemia. It is also used in the treatment of ventricular tachycardia. Lidocaine is an efficient anesthetic agent in ophthalmic surgeries as it is highly potent and has good tissue penetrability. Na+ channel blocker; class IB antiarrhythmic that is rapidly absorbed after parenteral administration.

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