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Catalog Number:
47358
CAS Number:
870992-10-2
1,3,5,7-Tetramethyl-8-(4-hydroxyphenyl)BODIPY
Purity:
≥ 95%
Documents
$520.00 /250MG
Pack Size Availability Price
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Product Information

1,3,5,7-Tetramethyl-8-(4-hydroxyphenyl)BODIPY is a versatile fluorescent dye known for its exceptional photostability and high quantum yield, making it an ideal choice for various applications in biological imaging and analytical chemistry. This compound exhibits strong absorption and emission properties in the visible spectrum, allowing researchers to utilize it in fluorescence microscopy, flow cytometry, and other imaging techniques. Its unique structure enhances its solubility in organic solvents, facilitating its use in a wide range of experimental conditions.

Moreover, 1,3,5,7-Tetramethyl-8-(4-hydroxyphenyl)BODIPY serves as an effective probe for studying cellular processes and interactions due to its ability to selectively bind to specific biomolecules. This capability opens avenues for applications in drug discovery, environmental monitoring, and the development of biosensors. With its robust performance and adaptability, this compound stands out as a valuable tool for researchers seeking reliable and efficient fluorescent markers in their work.

CAS Number
870992-10-2
Purity
≥ 95%
Molecular Formula
CC19H19BF2N2O
Molecular Weight
340.18
MDL Number
MFCD34167208
PubChem ID
139137151
Appearance
Red solid
Conditions
Store at RT
General Information
CAS Number
870992-10-2
Purity
≥ 95%
Molecular Formula
CC19H19BF2N2O
Molecular Weight
340.18
MDL Number
MFCD34167208
PubChem ID
139137151
Appearance
Red solid
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,3,5,7-Tetramethyl-8-(4-hydroxyphenyl)BODIPY is widely utilized in research focused on:

  • Fluorescent Imaging: This compound is an excellent fluorescent dye, making it ideal for biological imaging applications. Researchers use it to label cells and tissues, allowing for detailed visualization under a fluorescence microscope.
  • Photodynamic Therapy: Its strong absorption properties make it suitable for photodynamic therapy in cancer treatment. By targeting cancer cells and activating the dye with light, it can help destroy malignant tissues while minimizing damage to surrounding healthy cells.
  • Sensor Development: The compound is used in the development of sensors for detecting metal ions and other analytes. Its fluorescent properties change in response to specific environmental conditions, providing a reliable method for monitoring pollutants.
  • Bioconjugation: Researchers leverage its reactive functional groups for bioconjugation, allowing for the attachment of biomolecules. This is particularly useful in creating targeted drug delivery systems and enhancing the efficacy of therapeutic agents.
  • Solar Energy Applications: The compound's unique optical properties are being explored in the development of organic solar cells. Its ability to absorb light efficiently can improve the energy conversion efficiency of solar panels.

Citations