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Tetracaine-d6

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Catalog No. TMIJ-0246Cas No. 756771-02-5

Tetracaine-d6 is a deuterated compound of Tetracaine. Tetracaine has a CAS number of 94-24-6. Tetracaine is a powerful local anesthetic that alters the function of calcium releasing channels (lanine receptors) that control the release of calcium stored in cells.

Tetracaine-d6
Other Forms of Tetracaine-d6:
Tetracaine hydrochlorideT1198136-47-0
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Tetracaine-d6

😃Good
Catalog No. TMIJ-0246Cas No. 756771-02-5
Tetracaine-d6 is a deuterated compound of Tetracaine. Tetracaine has a CAS number of 94-24-6. Tetracaine is a powerful local anesthetic that alters the function of calcium releasing channels (lanine receptors) that control the release of calcium stored in cells.
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Product Introduction

Bioactivity
Description
Tetracaine-d6 is a deuterated compound of Tetracaine. Tetracaine has a CAS number of 94-24-6. Tetracaine is a powerful local anesthetic that alters the function of calcium releasing channels (lanine receptors) that control the release of calcium stored in cells.
Chemical Properties
Molecular Weight270.40
FormulaC15H18D6N2O2
Cas No.756771-02-5
Storage & Solubility Information
StorageShipping with blue ice.

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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