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AAT Bioquest

XFD680 azide

Product key features

  • Ex/Em: 681/704 nm
  • Extinction coefficient:184,000 cm-1M-1
  • Superior Fluorescence Performance: High quantum yield, exceptional photostability, and pH-independent fluorescence across pH 4–11.
  • Reactive Group: Azide
  • Click Chemistry Conjugation: Efficiently and rapidly labels terminal alkynes via CuAAC and copper-free SPAAC
  • High Water-Solubility: Prevents aggregation and enhances signal clarity for advanced imaging and live-cell applications

Product description

XFD680, manufactured by AAT Bioquest, is a bright near-infrared fluorescent dye structurally equivalent to Alexa Fluor™ 680 (ThermoFisher). It exhibits a high fluorescence quantum yield, excellent photostability, and superior aqueous solubility, ensuring consistent and reliable performance in various applications. Its pH-independent fluorescence across a broad range (pH 4–11) allows it to maintain stability under diverse experimental conditions. The dye also enables high molar ratio protein conjugation with minimal self-quenching, producing brighter conjugates and enhancing detection sensitivity. Its long-wavelength emission minimizes interference from autofluorescent background signals, enabling accurate detection in complex biological systems.

XFD680 is optimized for red laser excitation and is compatible with flow cytometers equipped with spectral detection systems. It delivers robust and uniform labeling, with high signal intensity and reproducibility, making it ideal for fluorescence imaging, flow cytometry, and other analytical techniques. XFD680 is also widely utilized in advanced applications such as multiplexed western blot detection and stochastic optical reconstruction microscopy (STORM), where its superior photophysical properties enhance resolution and sensitivity.

The azide derivative of XFD680 is widely used for labeling terminal alkynes on peptides, antibodies, and other biomolecules via click chemistry. It participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO- or BCN-containing molecules.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
XFD488 azide *Same Structure to Alexa Fluor™ 488 azide*499520710000.9210.300.11
XFD555 azide5535681500000.110.080.08
XFD635 azide633647140,000---
XFD647 Azide6506712700000.331-0.03
XFD680 TCO6817041840000.3610.000.05
XFD680 Tetrazine6817041840000.3610.000.05
XFD700 azide6967191920000.2510.000.07
XFD750 azide7527762400000.1210.000.04
XFD790 azide782805260,000-0.090.08
Page updated on April 15, 2025

Ordering information

Price
Unit size
Catalog Number70104
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Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
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Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.00

Correction Factor (280 nm)

0.05

Extinction coefficient (cm -1 M -1)

184000

Excitation (nm)

681

Emission (nm)

704

Quantum yield

0.361

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
Schematic illustrating the azide–alkyne cycloaddition (“click chemistry”) between an azide‐functionalized dye and an alkyne‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions and tolerates a wide range of functional groups.
Schematic illustrating the azide–alkyne cycloaddition (“click chemistry”) between an azide‐functionalized dye and an alkyne‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions and tolerates a wide range of functional groups.
Schematic illustrating the azide–alkyne cycloaddition (“click chemistry”) between an azide‐functionalized dye and an alkyne‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions and tolerates a wide range of functional groups.