2,5-Dioxopyrrolidin-1-yl pyrene-1-carboxylate

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Reagent Code: #130008
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CAS Number 204705-13-5

science Other reagents with same CAS 204705-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.33 g/mol
Formula C₂₁H₁₃NO₄
badge Registry Numbers
MDL Number MFCD32069527
thermostat Physical Properties
Boiling Point 555.2±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.48±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas, Light-proof

description Product Description

Used as a fluorescent labeling agent in biochemical and analytical applications. Its pyrene moiety provides strong fluorescence with high quantum yield, making it suitable for detecting and tracking biomolecules such as proteins and nucleic acids. The compound reacts with primary amines on target molecules to form stable amide bonds, allowing for covalent attachment of the fluorophore. Commonly employed in fluorescence spectroscopy, imaging, and immunoassays where sensitive detection is required. Also utilized in the development of fluorescent probes and sensors due to its environmental sensitivity and long fluorescence lifetime.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,790.00
inventory 250mg
10-20 days ฿18,180.00
inventory 1g
10-20 days ฿46,080.00

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2,5-Dioxopyrrolidin-1-yl pyrene-1-carboxylate
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Used as a fluorescent labeling agent in biochemical and analytical applications. Its pyrene moiety provides strong fluorescence with high quantum yield, making it suitable for detecting and tracking biomolecules such as proteins and nucleic acids. The compound reacts with primary amines on target molecules to form stable amide bonds, allowing for covalent attachment of the fluorophore. Commonly employed in fluorescence spectroscopy, imaging, and immunoassays where sensitive detection is required. Also ut

Used as a fluorescent labeling agent in biochemical and analytical applications. Its pyrene moiety provides strong fluorescence with high quantum yield, making it suitable for detecting and tracking biomolecules such as proteins and nucleic acids. The compound reacts with primary amines on target molecules to form stable amide bonds, allowing for covalent attachment of the fluorophore. Commonly employed in fluorescence spectroscopy, imaging, and immunoassays where sensitive detection is required. Also utilized in the development of fluorescent probes and sensors due to its environmental sensitivity and long fluorescence lifetime.

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