53213-98-2

Usage

Uses

Used in Research and Laboratory Settings:
2-[(1E,3E)-5-(3,3-DIMETHYL-1-PROPYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)-1,3-PENTADIENYL]-3,3-DIMETHYL-1-PROPYL-3H-INDOLIUM IODIDE is used as a staining agent for its fluorescent properties, allowing for the visualization and analysis of biological tissues and structures.
Used in Histology and Cytochemistry:
In the field of histology and cytochemistry, 2-[(1E,3E)-5-(3,3-DIMETHYL-1-PROPYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)-1,3-PENTADIENYL]-3,3-DIMETHYL-1-PROPYL-3H-INDOLIUM IODIDE serves as a vital component in staining processes, facilitating the examination of cellular and tissue structures.
Used in Medical Imaging and Diagnostics:
2-[(1E,3E)-5-(3,3-DIMETHYL-1-PROPYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)-1,3-PENTADIENYL]-3,3-DIMETHYL-1-PROPYL-3H-INDOLIUM IODIDE is used as a potential agent in medical imaging and diagnostics, leveraging its fluorescent properties to enhance the visualization of biological processes and structures for diagnostic purposes.

InChI:InChI=1/C31H39N2.HI/c1-7-22-32-26-18-14-12-16-24(26)30(3,4)28(32)20-10-9-11-21-29-31(5,6)25-17-13-15-19-27(25)33(29)23-8-2;/h9-21H,7-8,22-23H2,1-6H3;1H/q+1;/p-1

Upstream product

• 23769-16-6 phenyl[3-phenylaminoprop-2-en-1-ylidene]ammonium chloride 
• 20205-29-2 2,3,3-trimethyl-1-propyl-3H-indolium iodide 

Relevant academic research and scientific papers

COLORED COMPOSITION, COLORED CURED FILM, AND DISPLAY ELEMENT

PROBLEM TO BE SOLVED: To provide a colored composition containing a cyanine dye as a colorant and having good storage stability. SOLUTION: The colored composition comprises (A) a colorant, (B) a binder resin, and (C) a polymerizable compound. The (A) colorant comprises a compound having a structure represented by formula (1) below and a compound having a structure represented by formula (2) below, in which the content of the compound having a structure represented by formula (2) is 0.001 mass% or more with respect to the total content of the compound having a structure represented by formula (1) and the compound having a structure represented by formula (2). In formulae (1) and (2), ring Z1, ring Z2, ring Z3, and ring Z4 each independently represent a substituted or unsubstituted heterocycle; R1 to R6 each independently represent a hydrogen atom, a halogen atom, or a substituted or unsubstituted hydrocarbon group; and when R1, R2, R4, and R5 are present in plural numbers, they can be the same or different from one another; p represents 1 or 2; and q represents an integer of 2 or more when p is 1, and represents an integer of 3 or more when p is 2. COPYRIGHT: (C)2015,JPO&INPIT

Pentamethinium fluorescent probes: The impact of molecular structure on photophysical properties and subcellular localization

The performance of fluorescent probes arises from their structural basis. In this study, we report design and synthesis of a series of novel symmetrical γ-substituted pentamethinium fluorescent probes. Relationship between structure, photophysical propert