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Sulfachloropyridazine-d4

Catalog No. TMIH-0532

Sulfachloropyridazine-d4 is a deuterated compound of Sulfachloropyridazine. Sulfachloropyridazine has a CAS number of 80-32-0. Sulfachloropyridazine is a sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.

Sulfachloropyridazine-d4
Other Forms of Sulfachloropyridazine-d4:
Sulfachloropyridazine sodiumT7853623282-55-5
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SulfachloropyridazineT218480-32-0
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Sulfachloropyridazine-d4

Catalog No. TMIH-0532
Sulfachloropyridazine-d4 is a deuterated compound of Sulfachloropyridazine. Sulfachloropyridazine has a CAS number of 80-32-0. Sulfachloropyridazine is a sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.
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1 mg$1777-10 days
5 mgInquiry7-10 days
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Product Introduction

Bioactivity
Description
Sulfachloropyridazine-d4 is a deuterated compound of Sulfachloropyridazine. Sulfachloropyridazine has a CAS number of 80-32-0. Sulfachloropyridazine is a sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.
Chemical Properties
Molecular Weight288.75
FormulaC10H5D4ClN4O2S
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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