China Cook-Waite Lidocaine HCl 2% with Epinephrin HCl 1: 50, 000, Find details about China Lidocaine, Lidocaina from Cook-Waite Lidocaine HCl 2% with Epinephrin HCl 1: 50, 000
Lidocaine/Lidocaina HCl Basic
Product Name | Lidocaine HCl | ||
Purity | 99% Purity | ||
CAS number | 137-58-6/ 73-78-9 | Odor | Characteristic |
Color | White crystalline powder | Cas No. | 137-58-6 |
Molecular Formula | C14H22N2O | Molecular Weight | 234.34 |
Standard | USP36 Standard or Ep86, 99% Pure | ||
Function | Main functions are as follows: 1.Local anesthetic. 2. Treating Epilepsy. 3. Treating Asthma. | ||
Applications | Main applications are as follows: Applied in pharmaceuticalfields. | ||
Packing | 1kgor 5kg/bag, 25kg/drum | ||
Shelf Life | 24 months | ||
Storage | Store in sealed containers at cool & dry place. Protect from light, moisture and pest infestation |
Lidocaine HCl Description:
Local anesthetics. Local anesthetic intensity: tetracaine>tetracaine hcl>lidocaine>lidcaine hcl> benzocaine > procaine>procaine hcl, but there are corresponding side effects. Mainly used for surface anesthesia of the eyes, nose, throat and urinary tract.
It can cause convulsions after absorption, and then it is converted to respiratory depression, and is generally not used for anesthesia such as infiltration and conduction. Widely used in hospitals, dentists, tattoos, fitness and extended male ejaculation delays
Note: Lidocaine hydrochloride is dissolved in water and is generally used as a liquid. Lidocaine is not dissolved in water and is generally used as a cream.
Lidocaine HCl Applications:
1.Lidocaine, along with ethanol, ammonia, and acetic acid, has also been proven to be effective in treating jellyfish stings, both numbing the affected area and preventing further nematocyst discharge.
2.Lidocaine crosses the blood-brain and placental barriers, presumably by passive diffusion.
3.Lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys. Biotransformation includes oxidative N-dealkylation, ring hydroxylation, cleavage of the amide linkage, and conjugation. N-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide. The pharmacological/toxicological actions of these metabolites are similar to, but less potent than, those of Lidocaine. Approximately 90% of Lidocaine administered is excreted in the form of various metabolites, and less than 10% is excreted unchanged. The primary metabolite in urine is a conjugate of 4-hydroxy-2, 6-dimethylaniline.
English name | CAS | English name | CAS |
Benzocaine hydrochloride | 23239-88-5 | Procaine Hcl | 51-05-8 |
Pramoxine hydrochloride | 637-58-1 | Benzocaine | 94-09-7 |
Tetracaine | 94-24-6 | Lignocaine | 73-78-9 |
Tetracaine HCl | 136-47-0 | lidocaine hydrochloride | 73-78-9 |
Levobupivacaine HCl | 27262-48-2 | Ropivacaine hydrochloride | 132112-35-7 |
Dibucaine hydrochloride | 61-12-1 | Dibucaine hydrochloride | 61-12-1 |
Prilocaine Base | 751-50-6 | Bupivacaine | 2180-92-9 |
Prilocaine hydrochloride | 1786-81-8 | Bupivacaine hydrochloride | 14252-80-3 |
Proparacaine hydrochloride | 5875-06-9 | Dyclonine Hcl | 536-43-6 |
Procaine | 59-46-1 | Procaine penicillin | 6130-64-9 |
Procainamide hydrochloride | 614-39-1 | Aarticaine Hcl | 23964-57-0 |
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