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N3-TFBA-O2Oc
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Catalog No. T89751Cas No. 1993119-45-1
N3-TFBA-O2Oc is a photochemical probe comprising azide and aryl groups. This type of azidoaryl compound serves as a classical precursor to nitro compounds and has been utilized by Fleet et al as a versatile photophore for probing biological receptors. Specifically, N3-TFBA-O2Oc functions as a photo-crosslinker (λmax=258 nm) in studies involving estrogen receptors and for direct surface coating of carbon and organic polymers. Additionally, as a click chemistry reagent, N3-TFBA-O2Oc contains an azide group that reacts with molecules featuring an alkyne group through a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc). It can also engage in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups.
N3-TFBA-O2Oc
😃Good
Catalog No. T89751Cas No. 1993119-45-1
N3-TFBA-O2Oc is a photochemical probe comprising azide and aryl groups. This type of azidoaryl compound serves as a classical precursor to nitro compounds and has been utilized by Fleet et al as a versatile photophore for probing biological receptors. Specifically, N3-TFBA-O2Oc functions as a photo-crosslinker (λmax=258 nm) in studies involving estrogen receptors and for direct surface coating of carbon and organic polymers. Additionally, as a click chemistry reagent, N3-TFBA-O2Oc contains an azide group that reacts with molecules featuring an alkyne group through a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc). It can also engage in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
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Chemical Properties
Storage & Solubility Information
| Description | N3-TFBA-O2Oc is a photochemical probe comprising azide and aryl groups. This type of azidoaryl compound serves as a classical precursor to nitro compounds and has been utilized by Fleet et al as a versatile photophore for probing biological receptors. Specifically, N3-TFBA-O2Oc functions as a photo-crosslinker (λmax=258 nm) in studies involving estrogen receptors and for direct surface coating of carbon and organic polymers. Additionally, as a click chemistry reagent, N3-TFBA-O2Oc contains an azide group that reacts with molecules featuring an alkyne group through a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc). It can also engage in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups. |
| Molecular Weight | 380.25 |
| Formula | C13H12F4N4O5 |
| Cas No. | 1993119-45-1 |
| Smiles | [N-]=[N+]=NC1=C(F)C(F)=C(C(=O)NCCOCCOCC(=O)O)C(F)=C1F |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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