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|Packing:||Discreet Ways Of Packing For Customs Pass Guaranteed||ProductionCapacity:||1000 Kilogram/Month|
|Express Way:||EMS, FedEx, TNT, DHL, Hkems||Appearance:||White Crystalline Powder|
|Molecular Formula:||C14H23N2O||Molecular Formula:||235.3447|
|Synonyms:||Lignocaine, Lidocaine, Xylocaine, Lidocaine Base||EINECS:||205-302-8|
99% Min Raw Powder Lidocaine Base CAS 137-58-6 Lidocaine For Pain Killer And Local Anesthetics
Lidocaine Quick Detail:
|Synonyms||2-(Diethylamino)-2',6'-acetoxylidide;2-(diethylamino)-2',6'-acetoxylidide;2-(diethylamino)-n-(2,6-dimethylphenyl)-acetamid;2',6'-Acetoxylidide, 2-(diethylamino)-;6'-acetoxylidide,2-(diethylamino)-2;Acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl)-;Acetamide,2-(diethylamino)-N-(2,6-dimethylphenyl)-;a-Diethylamino-2,6-acetoxylidide|
|Usage||Lidocaine (Alphacaine)is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. Histamine is responsible for many features of allergic reactions. Lidocaine (Alphacaine)is a second-generation antihistamine agent closely st|
Lidocaine is an antiarrhythmic medication of the class Ib type. Lidocaine works by blocking sodium channels and thus decreasing the rate of contractions of the heart. When used locally as a numbing agent, local neurons cannot signal the brain.
Topical lidocaine has been shown in some patients to relieve the pain of postherpetic neuralgia (a
Complication of shingles), though there is not enough study evidence to recommend it as a first-line
Treatment. IV lidocaine also has uses as a temporary fix for tinnitus. Although not completely curing
The disorder, it has been shown to reduce the effects by around two thirds.
Lidocaine hydrochloride injection administered intravenously or intramuscularly, is specifically indicated
In the acute management of ventricular arrhythmias such as those occurring in relation to acute
Myocardial infarction, or during cardiac manipulation, such as cardiac surgery.
|Arrhythmias||Initial dose: 1 to 1.5 mg/kg/dose intravenously (IV) given over 2 to 3 minutes.
Prehospital post-myocardial infarction (MI) antiarrhythmic prophylaxis: 300 mg intramusculary once.
|Ventricular Fibrillation||Initial dose: 1 to 1.5 mg/kg/dose intravenously (IV).
Prevention of ventricular fibrillation: IV bolus: 0.5 mg/kg/dose; repeat every 5 to 10 minutes to a total dose of 2 mg/kg.
|Anesthesia||Anesthesia, local injectable: Dose varies with procedure, degree of anesthesia needed, vascularity of tissue, duration of anesthesia required, and physical condition of patient; maximum dose: 4.5 mg/kg/dose; do not repeat within 2 hours.|
Suggestion:please use it with the doctor's instructions.
|Procaine||White crystalline powder; odorless, slightly bitter taste, then there is a sense of paralysis; case of light yellow color gradient.||Procaine is commonly used local anesthetic. Mucosal penetration is weak. Generally not used for topical anesthesia, often local injection for anesthesia, conduction anesthesia, spinal anesthesia and epidural anesthesia.|
|Lidocaine||Soluble in alcohol, ether, benzene, chloroform and oils, insoluble in water||It is currently the most widely used local anesthetic. At the same concentration as compared with procaine, lidocaine has a rapid onset, the role of a strong and lasting, strong penetration and a large range of security features, but no expansion of the role and the organization almost no irritation. Can be used for various forms of local anesthesia, there is all-round anesthetic known, mainly for conduction anesthesia and epidural anesthesia. The drug can also be used for the treatment of arrhythmia, procaine allergy may use this drug.|
|Tetracaine(Dicaine)||White crystal or crystalline powder; odorless, slightly bitter taste, sense of Ma tongue.
This product is soluble in water, soluble in ethanol, insoluble in ether.
|Its chemical structure is similar with Procaine, are lipids local anesthetic. The drug penetrating the mucous membrane strong, commonly used in topical anesthesia. 0.5% to 1% solution drops, no corneal damage and other adverse effects of the drug can also be used for conduction anesthesia, spinal anesthesia and epidural anesthesia, due to toxicity, generally not used for anesthesia.|
|Ropivacaine||White or white crystal or crystalline powder; odorless.
This product is soluble in ethanol, dissolved in water, almost insoluble in ether.
|Its chemical structure is similar to bupivacaine, which blocks pain stronger role and the role of the movement is weak, short duration of action, myocardial toxicity than bupivacaine, with a clear vasoconstrictor effect. Suitable for epidural, brachial plexus block and local anesthesia. Almost no effect on the uterine and placental blood flow, it applies to obstetric anesthesia.|
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