N-(3-Triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide

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N-(3-Triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide

N-(3-Triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide | 149838-22-2

Catalog Number A16-0079
Category Nerve Terminal Probes
Molecular Formula C30H49Br2N3
Molecular Weight 611.55
Catalog Number Size Price Quantity
A16-0079 -- $--

Product Introduction

A membrane-permeant fluorescent probe that is useful in cell biology and neurobiology for investigation of synaptic activity at synapses and at neuromuscular junctions. This probe is non-fluorescent until it binds to membrane.

Chemical Information

Synonyms NeurotransGreen C4; MM1-43; 3-[4-[(E)-2-[4-(dibutylamino)phenyl]ethenyl]pyridin-1-ium-1-yl]propyl-triethylazanium dibromide
Canonical SMILES CCCCN(CCCC)C1=CC=C(C=C1)C=CC2=CC=[N+](C=C2)CCC[N+](CC)(CC)CC.[Br-].[Br-]
InChI InChI=1S/C30H49N3.2BrH/c1-6-11-23-32(24-12-7-2)30-18-16-28(17-19-30)14-15-29-20-25-31(26-21-29)22-13-27-33(8-3,9-4)10-5;;/h14-21,25-26H,6-13,22-24,27H2,1-5H3;2*1H/q+2;;/p-2
InChI Key VZUVCAGXYLMFEC-UHFFFAOYSA-L
  • Product Specification
  • Application
Excitation 541
Emission 567

N-(3-Triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide is a fluorescent dye with versatile applications in biological and chemical research. Here are some key applications of this compound:

Cell Imaging: This fluorescent dye is used extensively in live cell imaging to visualize cellular structures and processes. By tagging cellular components such as proteins or membranes, researchers can observe real-time cellular dynamics under a microscope. This provides valuable insights into cellular functions, interactions, and morphological changes.

Flow Cytometry: The fluorescent properties of this compound make it suitable for use in flow cytometry, a technique used to analyze the physical and chemical characteristics of cells or particles. When conjugated to antibodies or other ligands, it allows for the identification and quantification of specific cell populations. This is crucial in immunology, cancer research, and various diagnostic applications.

Molecular Probes: N-(3-Triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide acts as a molecular probe for studying nucleic acid interactions. It can intercalate with DNA or RNA, making it useful for fluorescence-based assays that monitor nucleic acid hybridization, melting, or other conformational changes. This helps in advancing our understanding of genetic materials and their functions.

Fluorescent Sensors: This compound can be employed in the development of fluorescent sensors for detecting various analytes, such as ions, small molecules, or environmental contaminants. By designing sensors that change their fluorescence properties in response to specific targets, researchers can create sensitive and specific detection methods. These sensors have applications in environmental monitoring, medical diagnostics, and chemical analysis.

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