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Catalog Number:
47556
CAS Number:
14696-39-0
1,1'-Diethyl-3,3,3',3'-tetramethylindocarbocyanine iodide
Purity:
≥ 98% (HPLC)
Synonym(s):
Astrophloxine
Documents
$127.20 /1G
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Product Information

1,1'-Diethyl-3,3,3',3'-tetramethylindocarbocyanine iodide is a highly versatile fluorescent dye known for its exceptional photostability and strong absorption properties. This compound is widely utilized in various applications, particularly in biological research, where it serves as a vital tool for fluorescence microscopy and flow cytometry. Its ability to emit bright fluorescence makes it ideal for labeling cells and biomolecules, allowing researchers to visualize and track cellular processes with precision. Additionally, its unique structure provides a high degree of specificity in binding to target molecules, enhancing the accuracy of experimental results.

In the field of diagnostics, 1,1'-Diethyl-3,3,3',3'-tetramethylindocarbocyanine iodide is employed in assays and imaging techniques, facilitating the detection of specific proteins and nucleic acids. Its compatibility with various imaging systems further broadens its application scope, making it a preferred choice among researchers and industry professionals. With its robust performance and reliability, this compound stands out as an essential reagent for advancing scientific discovery and innovation.

Synonyms
Astrophloxine
CAS Number
14696-39-0
Purity
≥ 98% (HPLC)
Molecular Formula
C27H33IN2
Molecular Weight
512.48
MDL Number
MFCD22573598
PubChem ID
9871053
Appearance
Red to purple powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Astrophloxine
CAS Number
14696-39-0
Purity
≥ 98% (HPLC)
Molecular Formula
C27H33IN2
Molecular Weight
512.48
MDL Number
MFCD22573598
PubChem ID
9871053
Appearance
Red to purple powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,1'-Diethyl-3,3,3',3'-tetramethylindocarbocyanine iodide is widely utilized in research focused on:

  • Fluorescent Imaging: This compound is commonly used as a fluorescent dye in biological imaging, allowing researchers to visualize cellular processes and structures with high sensitivity and specificity.
  • Flow Cytometry: It serves as a vital reagent in flow cytometry applications, helping to analyze cell populations by tagging specific cellular components, thus providing insights into cell health and function.
  • Bioconjugation: The chemical is effective for labeling biomolecules, enabling the study of protein interactions and cellular pathways, which is crucial in drug development and molecular biology.
  • Photodynamic Therapy: Its properties make it suitable for applications in photodynamic therapy, where it can be used to target and destroy cancer cells through light activation.
  • Environmental Monitoring: The compound can be employed in environmental studies to track pollutants and understand their effects on ecosystems, making it valuable for researchers in environmental science.

Citations