6-carboxy-4',5'-dichloro-2',7'-dimethoxyfluorescein

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Reagent Code: #162439
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CAS Number 82855-40-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 505.25786 g/mol
Formula C₂₃H₁₄Cl₂O₉
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a fluorescent probe in biochemical and cellular assays due to its high sensitivity and photostability. Its carboxy and methoxy groups enhance water solubility and allow for easy conjugation to biomolecules such as antibodies, proteins, and nucleic acids. Commonly employed in fluorescence microscopy, flow cytometry, and immunoassays for detecting specific targets in complex biological samples. The dichloro substitution increases fluorescence quantum yield and improves resistance to photobleaching, making it suitable for long-term imaging experiments. Also utilized in pH sensing applications because of its fluorescence intensity changes in response to environmental pH shifts.

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Test Parameter Specification
Appearance solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,540.00
inventory 250mg
10-20 days ฿14,490.00
inventory 1g
10-20 days ฿39,990.00

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6-carboxy-4',5'-dichloro-2',7'-dimethoxyfluorescein
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Used primarily as a fluorescent probe in biochemical and cellular assays due to its high sensitivity and photostability. Its carboxy and methoxy groups enhance water solubility and allow for easy conjugation to biomolecules such as antibodies, proteins, and nucleic acids. Commonly employed in fluorescence microscopy, flow cytometry, and immunoassays for detecting specific targets in complex biological samples. The dichloro substitution increases fluorescence quantum yield and improves resistance to photo

Used primarily as a fluorescent probe in biochemical and cellular assays due to its high sensitivity and photostability. Its carboxy and methoxy groups enhance water solubility and allow for easy conjugation to biomolecules such as antibodies, proteins, and nucleic acids. Commonly employed in fluorescence microscopy, flow cytometry, and immunoassays for detecting specific targets in complex biological samples. The dichloro substitution increases fluorescence quantum yield and improves resistance to photobleaching, making it suitable for long-term imaging experiments. Also utilized in pH sensing applications because of its fluorescence intensity changes in response to environmental pH shifts.

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