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Catalog Number:
41883
CAS Number:
76877-33-3
7-Diéthylamino-3-(4-maléimidophényl)-4-méthylcoumarine
Grade:
adapté à l'hématologie et à l'histologie
Purity:
≥ 95 % (HPLC)
Synonym(s):
1 H -Pyrrole-2,5-dione, 1-(4-(7-(diéthylamino)-4-méthyl-2-oxo-2 H -1-benzopyran-3-yl)phényl)-
Temperature Sensitive
Documents
$412.82 /25 mg
Taille
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Product Information

7-Diethylamino-3-(4-maleimidophenyl)-4-methylcoumarin is a versatile fluorescent dye widely utilized in bioconjugation and imaging applications. This compound features a unique maleimide group that allows for selective conjugation to thiol-containing biomolecules, making it an excellent choice for labeling proteins, peptides, and antibodies. Its strong fluorescence properties enable researchers to visualize cellular processes and track biomolecular interactions with high sensitivity and specificity.

In addition to its applications in research, this compound is also valuable in the development of diagnostic tools and therapeutic agents. Its ability to form stable conjugates with various biomolecules enhances the efficacy of drug delivery systems and targeted therapies. With its exceptional photostability and brightness, 7-Diethylamino-3-(4-maleimidophenyl)-4-methylcoumarin stands out among similar compounds, providing researchers with a reliable tool for advancing their studies in molecular biology and biochemistry.

Synonyms
1 H -Pyrrole-2,5-dione, 1-(4-(7-(diéthylamino)-4-méthyl-2-oxo-2 H -1-benzopyran-3-yl)phényl)-
CAS Number
76877-33-3
Purity
≥ 95 % (HPLC)
Grade
adapté à l'hématologie et à l'histologie
Molecular Formula
C24H22N2O4
Molecular Weight
402.44
MDL Number
MFCD00077334
PubChem ID
122042
Appearance
Solide jaune
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
1 H -Pyrrole-2,5-dione, 1-(4-(7-(diéthylamino)-4-méthyl-2-oxo-2 H -1-benzopyran-3-yl)phényl)-
CAS Number
76877-33-3
Purity
≥ 95 % (HPLC)
Grade
adapté à l'hématologie et à l'histologie
Molecular Formula
C24H22N2O4
Molecular Weight
402.44
MDL Number
MFCD00077334
PubChem ID
122042
Appearance
Solide jaune
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

7-Diethylamino-3-(4-maleimidophenyl)-4-methylcoumarin is widely utilized in research focused on:

  • Fluorescent Probes: This compound is used as a fluorescent probe in biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Bioconjugation: Its maleimide group enables efficient conjugation to thiol-containing biomolecules, making it valuable in the development of targeted drug delivery systems and diagnostic tools.
  • Photodynamic Therapy: The compound's fluorescence properties are harnessed in photodynamic therapy, where it can help in the treatment of cancer by selectively targeting tumor cells.
  • Sensor Development: It serves as a key component in the creation of sensors for detecting specific biomolecules, enhancing the accuracy and reliability of biosensors in clinical diagnostics.
  • Research in Molecular Biology: This chemical facilitates studies in molecular biology, particularly in tracking protein interactions and dynamics within live cells, providing insights into cellular mechanisms.

Citations