1-(5-Carboxypentyl)-2-(2-(3-(2-(1-(5-carboxypentyl)-3,3-dimethylindolin-2-ylidene)ethylidene)-2-chlorocyclohex-1-en-1-yl)vinyl)-3,3-dimethyl-3H-indol-1-ium bromide

98%

Reagent Code: #163744
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CAS Number 172971-76-5

science Other reagents with same CAS 172971-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 764.24 g/mol
Formula C₄₂H₅₂BrClN₂O₄
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a near-infrared fluorescent probe in biological imaging due to its strong absorption and emission in the NIR region. Ideal for detecting cellular structures and monitoring biological processes in real time, especially in deep tissue imaging where longer wavelengths reduce background autofluorescence and light scattering. Its carboxyl groups allow for easy conjugation to biomolecules such as antibodies, peptides, or proteins, enabling targeted labeling in immunoassays and molecular sensing. Also applied in photodynamic therapy research and as a sensor in fluorescence-based detection systems for metal ions or pH changes in living cells.

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Test Parameter Specification
Appearance Light green to green or purple solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,080.00
inventory 250mg
10-20 days ฿15,810.00
inventory 1g
10-20 days ฿46,510.00
inventory 100mg
10-20 days ฿8,560.00

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1-(5-Carboxypentyl)-2-(2-(3-(2-(1-(5-carboxypentyl)-3,3-dimethylindolin-2-ylidene)ethylidene)-2-chlorocyclohex-1-en-1-yl)vinyl)-3,3-dimethyl-3H-indol-1-ium bromide
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Used as a near-infrared fluorescent probe in biological imaging due to its strong absorption and emission in the NIR region. Ideal for detecting cellular structures and monitoring biological processes in real time, especially in deep tissue imaging where longer wavelengths reduce background autofluorescence and light scattering. Its carboxyl groups allow for easy conjugation to biomolecules such as antibodies, peptides, or proteins, enabling targeted labeling in immunoassays and molecular sensing. Also a

Used as a near-infrared fluorescent probe in biological imaging due to its strong absorption and emission in the NIR region. Ideal for detecting cellular structures and monitoring biological processes in real time, especially in deep tissue imaging where longer wavelengths reduce background autofluorescence and light scattering. Its carboxyl groups allow for easy conjugation to biomolecules such as antibodies, peptides, or proteins, enabling targeted labeling in immunoassays and molecular sensing. Also applied in photodynamic therapy research and as a sensor in fluorescence-based detection systems for metal ions or pH changes in living cells.

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