1,4-CIS-1-(1-CYCLOOCTEN-1-YLMETHYL)-4-[[(2,7-DICHLORO-9H-XANTHEN-9-YL)CARBONYL]AMINO]-1-ETHYLPIPERIDINIUM IODIDE

98%

Reagent Code: #156707
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CAS Number 353791-85-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 655.44 g/mol
Formula C₃₀H₃₇Cl₂IN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a fluorescent probe in biological imaging and cellular assays. Its structure allows it to bind selectively to specific cellular components, making it valuable for tracking membrane dynamics and studying receptor localization. The compound’s fluorescence properties change in response to environmental polarity, enabling researchers to monitor changes in cellular microenvironments. It is also employed in flow cytometry and confocal microscopy due to its strong emission signal and photostability. Its iodide salt form enhances solubility in aqueous buffers, facilitating use in live-cell imaging with minimal cytotoxicity at working concentrations.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿18,900.00
inventory 50mg
10-20 days ฿50,000.00

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1,4-CIS-1-(1-CYCLOOCTEN-1-YLMETHYL)-4-[[(2,7-DICHLORO-9H-XANTHEN-9-YL)CARBONYL]AMINO]-1-ETHYLPIPERIDINIUM IODIDE
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Used primarily as a fluorescent probe in biological imaging and cellular assays. Its structure allows it to bind selectively to specific cellular components, making it valuable for tracking membrane dynamics and studying receptor localization. The compound’s fluorescence properties change in response to environmental polarity, enabling researchers to monitor changes in cellular microenvironments. It is also employed in flow cytometry and confocal microscopy due to its strong emission signal and photostab

Used primarily as a fluorescent probe in biological imaging and cellular assays. Its structure allows it to bind selectively to specific cellular components, making it valuable for tracking membrane dynamics and studying receptor localization. The compound’s fluorescence properties change in response to environmental polarity, enabling researchers to monitor changes in cellular microenvironments. It is also employed in flow cytometry and confocal microscopy due to its strong emission signal and photostability. Its iodide salt form enhances solubility in aqueous buffers, facilitating use in live-cell imaging with minimal cytotoxicity at working concentrations.

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