2,3-Bis(4-methoxyphenyl)-5-(4-cyanophenyl)tetrazolium Chloride

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Reagent Code: #147372
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CAS Number 151390-91-9

science Other reagents with same CAS 151390-91-9

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scatter_plot Molecular Information
Weight 419.87 g/mol
Formula C₂₂H₁₈ClN₅O₂
badge Registry Numbers
MDL Number MFCD00060131
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a vital reagent in cell viability and proliferation assays, particularly in tetrazolium-based assay formats such as the MTT assay. It serves as an electron acceptor that is reduced by metabolically active cells into a colored formazan product, which can be quantified spectrophotometrically. This allows researchers to assess cell health, cytotoxicity, and the effectiveness of pharmaceutical compounds in vitro. Due to its ability to penetrate cell membranes and undergo enzymatic reduction primarily in mitochondria, it is widely employed in cancer research, drug screening, and toxicology studies. The presence of the cyanophenyl and methoxyphenyl groups enhances solubility and stability, improving assay sensitivity and reproducibility.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿740.00
inventory 50mg
10-20 days ฿1,281.50
inventory 100mg
10-20 days ฿3,950.00

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2,3-Bis(4-methoxyphenyl)-5-(4-cyanophenyl)tetrazolium Chloride
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Used as a vital reagent in cell viability and proliferation assays, particularly in tetrazolium-based assay formats such as the MTT assay. It serves as an electron acceptor that is reduced by metabolically active cells into a colored formazan product, which can be quantified spectrophotometrically. This allows researchers to assess cell health, cytotoxicity, and the effectiveness of pharmaceutical compounds in vitro. Due to its ability to penetrate cell membranes and undergo enzymatic reduction primarily

Used as a vital reagent in cell viability and proliferation assays, particularly in tetrazolium-based assay formats such as the MTT assay. It serves as an electron acceptor that is reduced by metabolically active cells into a colored formazan product, which can be quantified spectrophotometrically. This allows researchers to assess cell health, cytotoxicity, and the effectiveness of pharmaceutical compounds in vitro. Due to its ability to penetrate cell membranes and undergo enzymatic reduction primarily in mitochondria, it is widely employed in cancer research, drug screening, and toxicology studies. The presence of the cyanophenyl and methoxyphenyl groups enhances solubility and stability, improving assay sensitivity and reproducibility.

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