| Customization: | Available |
|---|---|
| Powder: | Yes |
| Customized: | Non-Customized |
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Tetracaine HCl Basic Information:
| Product name | Tetracaine hcl ( Tetracaine Hrdrochloride) |
| CAS No. | 136-47-0 |
| Molecular formula | C15H25ClN2O2 |
| Molecular weight | 300.82 |
| EINECS number | 205-248-5 |
| Melting point | 149°C |
| Storage condition | Room Temperature |
| Purity | >99% |
| Standard | Pharmaceutical Grade |
| Appearance | White or almost white crystal powder |
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We guarantee that your package will be delivered to your hands 100% safely within 3-5 days to USA by DHL UPS/USPS 7~15days,Europe double clearance ways 100% DDP Success delivery . And you won't have any loss when you work with us, 100% safe and easy !
100% Safe delivery door to door service shipping.We also can supply overseas warehouses for some big orders.
The Local anesthesia Powders All EP or USP standard from GMP workshops.
All including shipping DDP 100% success delivery.
Tips: hcl soluble in water, base insoluble in water. (Some Base dissolves in hot water!)
Local anesthesia strength: the anesthesia effect of some base is stronger than hcl)
Tetracaine>Lidocaine>Benzo1caine>Procaine
Pharmaceutical-Grade Anesthetic Purity HCl Powder CAS 136-47-0 - Tetracaine Lidocaine
Lidocaine hydrochloride is swiftly metabolized by the liver, with both metabolites and the unchanged drug being excreted via the kidneys. The biotransformation process encompasses oxidative N-dealkylation, ring hydroxylation, amide linkage cleavage, and conjugation. N-dealkylation, the primary pathway, produces the metabolites monoethylglycinexylidide and glycinexylidide, which have pharmacological and toxicological actions akin to, but less potent than, Lidocaine hydrochloride. Approximately 90% of administered Lidocaine hydrochloride is excreted as various metabolites, with less than 10% excreted unchanged. The main metabolite in urine is a conjugate of 4-hydroxy-2,6-dimethylaniline.
Lidocaine HCl is a powerful amide local anesthetic.
As the dosage increases, its efficacy or potential toxicity also increases, providing an anti-convulsive effect at sub-toxic plasma concentrations.
Blood concentrations exceeding 5μg/ml may induce convulsions.
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