logo
AAT Bioquest

XFD680 TCO

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: TCO
  • Click Chemistry Conjugation: Provides rapid and copper-free labeling of tetrazine-modified biomolecules
  • 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.

XFD680 TCO is particularly useful for labeling tetrazine-modified biomolecules under copper-free conditions. It reacts with tetrazine-functionalized molecules, forming a stable conjugate via a dihydropyrazine moiety. This click reaction is favored over others due to its extremely fast kinetics and higher yields under mild reaction conditions, making it a popular choice for researchers.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
XFD488 TCO499520730000.9210.30.11
XFD555 TCO5535681500000.110.080.08
XFD635 TCO633647140,000---
XFD647 TCO6506712390000.3310.000.03
XFD680 acid6817041840000.3610.000.05
XFD680 alkyne6817041840000.3610.000.05
XFD680 amine6817041840000.3610.000.05
XFD680 azide6817041840000.3610.000.05
XFD680 Tetrazine6817041840000.3610.000.05
XFD700 TCO6967191920000.2510.000.07
XFD750 TCO7527762400000.1210.000.04
XFD790 TCO782805260,000-0.090.08
Show More (3)
Page updated on April 15, 2025

Ordering information

Price
Unit size
Catalog Number70107
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
Technical SupportContact us
Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
Request quotation

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 strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a trans‐cyclooctene (TCO)–dye conjugate and a tetrazine‐modified biomolecule. The TCO–dye adduct selectively and rapidly couples with the tetrazine moiety on the biomolecule to form a stable linkage. This bioorthogonal “click chemistry” reaction is fast, selective, and well‐suited for biocompatible labeling applications.
Schematic illustrating the strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a trans‐cyclooctene (TCO)–dye conjugate and a tetrazine‐modified biomolecule. The TCO–dye adduct selectively and rapidly couples with the tetrazine moiety on the biomolecule to form a stable linkage. This bioorthogonal “click chemistry” reaction is fast, selective, and well‐suited for biocompatible labeling applications.
Schematic illustrating the strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a trans‐cyclooctene (TCO)–dye conjugate and a tetrazine‐modified biomolecule. The TCO–dye adduct selectively and rapidly couples with the tetrazine moiety on the biomolecule to form a stable linkage. This bioorthogonal “click chemistry” reaction is fast, selective, and well‐suited for biocompatible labeling applications.