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Mebeverine Acid-d5

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Catalog No. TMIH-0322Cas No. 2070015-30-2

Mebeverine Acid-d5 is a deuterated compound of Mebeverine Acid. Mebeverine Acid has a CAS number of 475203-77-1. Mebeverine acid is a secondary metabolite of Mebeverine and can be used as a marker of oral exposure to Mebeverine.

Mebeverine Acid-d5

Mebeverine Acid-d5

😃Good
Catalog No. TMIH-0322Cas No. 2070015-30-2
Mebeverine Acid-d5 is a deuterated compound of Mebeverine Acid. Mebeverine Acid has a CAS number of 475203-77-1. Mebeverine acid is a secondary metabolite of Mebeverine and can be used as a marker of oral exposure to Mebeverine.
Pack SizePriceAvailabilityQuantity
1 mg$4857-10 days
5 mg$1,4507-10 days
10 mg$2,4207-10 days
25 mg$4,4907-10 days
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Product Introduction

Bioactivity
Description
Mebeverine Acid-d5 is a deuterated compound of Mebeverine Acid. Mebeverine Acid has a CAS number of 475203-77-1. Mebeverine acid is a secondary metabolite of Mebeverine and can be used as a marker of oral exposure to Mebeverine.
Chemical Properties
Molecular Weight284.41
FormulaC16H25NO3
Cas No.2070015-30-2
Relative Density.no data available
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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