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Phenazopyridine hydrochloride

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Catalog No. T1386Cas No. 136-40-3
Alias Urodine, Pyridium, Phenazopyridine HCl

Phenazopyridine hydrochloride (Pyridium) is used orally as a urinary tract analgesic. Side effects of phenazopyridine hydrochloride administration can include nausea, interference with the oxygen-carrying capacity of red blood cells (methemoglobinemia), hemolytic anemia as well as renal and hepatic toxicity. It is reasonably anticipated to be a human carcinogen.

Phenazopyridine hydrochloride

Phenazopyridine hydrochloride

🥰Excellent
Purity: 99.83%
Catalog No. T1386Alias Urodine, Pyridium, Phenazopyridine HClCas No. 136-40-3
Phenazopyridine hydrochloride (Pyridium) is used orally as a urinary tract analgesic. Side effects of phenazopyridine hydrochloride administration can include nausea, interference with the oxygen-carrying capacity of red blood cells (methemoglobinemia), hemolytic anemia as well as renal and hepatic toxicity. It is reasonably anticipated to be a human carcinogen.
Pack SizePriceAvailabilityQuantity
50 mg36 €In Stock
100 mg44 €In Stock
200 mg62 €In Stock
1 mL x 10 mM (in DMSO)47 €In Stock
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Purity:99.83%
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Product Introduction

Bioactivity
Description
Phenazopyridine hydrochloride (Pyridium) is used orally as a urinary tract analgesic. Side effects of phenazopyridine hydrochloride administration can include nausea, interference with the oxygen-carrying capacity of red blood cells (methemoglobinemia), hemolytic anemia as well as renal and hepatic toxicity. It is reasonably anticipated to be a human carcinogen.
In vitro
Phenazopyridine directly inhibits the mechanical sensitivity of Aδ-fibers in the bladders of normal rats.
In vivo
Phenazopyridine enhances cell viability, strengthens neuronal cell differentiation, synchronizes the state of cell differentiation, and reduces the number of non-neuronal and undifferentiated cells.
AliasUrodine, Pyridium, Phenazopyridine HCl
Chemical Properties
Molecular Weight249.7
FormulaC11H12ClN5
Cas No.136-40-3
SmilesCl.Nc1ccc(\N=N\c2ccccc2)c(N)n1
Relative Density.1.2645 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 10 mg/mL (40.05 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.0048 mL20.0240 mL40.0481 mL200.2403 mL
5 mM0.8010 mL4.0048 mL8.0096 mL40.0481 mL
10 mM0.4005 mL2.0024 mL4.0048 mL20.0240 mL
20 mM0.2002 mL1.0012 mL2.0024 mL10.0120 mL

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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
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