Bis([1, 10-Phenanthroline)(4, 5, 9, 14-Tetraaza-benzo[b]triphenylene)ruthenium (II) dichloride

98%

Reagent Code: #152068
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CAS Number 132045-66-0

science Other reagents with same CAS 132045-66-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 814.70 g/mol
Formula C₄₂H₂₆Cl₂N₈Ru
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as a luminescent probe in DNA binding studies due to its strong affinity for duplex and G-quadruplex DNA structures. Its application spans bioanalytical chemistry and molecular biology, where it serves as a fluorescent sensor for detecting nucleic acid conformation changes. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species upon light activation. Additionally, it acts as a photosensitizer in solar energy conversion systems and artificial photosynthesis setups, leveraging its long-lived excited states and efficient electron transfer properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,700.00
inventory 250mg
10-20 days ฿13,030.00
inventory 1g
10-20 days ฿35,150.00

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Bis([1, 10-Phenanthroline)(4, 5, 9, 14-Tetraaza-benzo[b]triphenylene)ruthenium (II) dichloride
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Used as a luminescent probe in DNA binding studies due to its strong affinity for duplex and G-quadruplex DNA structures. Its application spans bioanalytical chemistry and molecular biology, where it serves as a fluorescent sensor for detecting nucleic acid conformation changes. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species upon light activation. Additionally, it acts as a photosensitizer in solar energy conversion systems and artificial photosynt

Used as a luminescent probe in DNA binding studies due to its strong affinity for duplex and G-quadruplex DNA structures. Its application spans bioanalytical chemistry and molecular biology, where it serves as a fluorescent sensor for detecting nucleic acid conformation changes. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species upon light activation. Additionally, it acts as a photosensitizer in solar energy conversion systems and artificial photosynthesis setups, leveraging its long-lived excited states and efficient electron transfer properties.

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