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ATTO 514 Tetrazine

Product key features

  • Ex/Em: 510/531 nm
  • Extinction coefficient: 115,000 cm-1M-1
  • Reactive group: Tetrazine
  • Click Chemistry Conjugation: Offers high yield and rapid, copper-free labeling of TCO-modified biomolecules
  • Superior Brightness & Stability: Provides robust quantum yield with high photostability and thermal stability
  • Excellent Hydrophilicity: Prevents aggregation and enhances signal clarity for advanced imaging and live-cell applications

Product description

ATTO 514 Tetrazine is manufactured by AAT Bioquest for research and development use. ATTO 514 tetrazine is particularly useful for labeling TCO-modified biomolecules under copper-free conditions, with the bright, green fluorescent ATTO 514 dye. It reacts with TCO-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.

ATTO 514 is a hydrophilic fluorescent dye characterized by excellent aqueous solubility, strong molar absorptivity, high fluorescence quantum yield, and notable thermal and photostability. These properties make it well-suited for advanced imaging techniques, including single-molecule detection and super-resolution microscopy methods such as PALM, dSTORM, and STED. ATTO 514 is also compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and other fluorescence-based assays. The dye is optimally excited within the 510–535 nm range, with the 514 nm line of an Argon-Ion laser providing efficient excitation.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 390 Tetrazine39047524000.900.460.09
ATTO 425 Tetrazine438484450000.900.190.17
ATTO 488 Tetrazine499520900000.800.220.09
ATTO 495 Tetrazine497525800000.20.450.37
ATTO 514 acid510531115,0000.850.210.08
ATTO 514 alkyne510531115,0000.850.210.08
ATTO 514 azide510531115,0000.850.210.08
ATTO 514 maleimide510531115,0000.850.210.08
ATTO 514 TCO510531115,0000.850.210.08
ATTO 532 Tetrazine5315521150000.900.220.11
ATTO 550 Tetrazine5535741200000.800.230.10
ATTO 565 Tetrazine5625891200000.900.270.12
ATTO 590 Tetrazine5926211200000.800.390.43
ATTO 594 Tetrazine6026211200000.850.260.51
ATTO 610 Tetrazine6156321500000.700.030.06
ATTO 620 Tetrazine61964112000010.510.040.06
ATTO 633 Tetrazine6296511300000.6410.040.05
ATTO 647 Tetrazine6466661200000.200.080.04
ATTO 647N Tetrazine6456631500000.6510.060.05
ATTO 655 Tetrazine6616791250000.310.240.08
ATTO 680 Tetrazine6796961250000.300.300.17
ATTO 700 Tetrazine6997151200000.250.260.41
Show More (13)

References

View all 50 references: Citation Explorer
Efficient Drug Release from Liposomes Introduced Tetrazine Derivatives with Pyrimidine Rings Using Click Chemistry.
Authors: Yamasaki, Mizuho and Munekane, Masayuki and Kannaka, Kento and Sano, Kohei and Yamasaki, Toshihide and Mukai, Takahiro
Journal: Chemical & pharmaceutical bulletin (2025): 108-111
Bioorthogonal Post-Labeling Reveals Nuclear Localization of a Highly Cytotoxic Half-sandwich Ir(III) Tetrazine Complex in Live Cells.
Authors: Annunziata, Alfonso and Amhaz, Sadek and Forté, Jérémy and Gontard, Geoffrey and Morichon, Romain and Sobczak-Thépot, Joëlle and Salmain, Michele
Journal: Chembiochem : a European journal of chemical biology (2025): e202500090
A Tetrazine Amplification System for Visual Detection of Trace Analytes via Click-Release Reactions.
Authors: Li, Jing and Cheng, Mingxin and Zhang, Hongbo and Wang, Yichen and Guo, Weiwei and Zheng, Yueqin
Journal: Angewandte Chemie (International ed. in English) (2025): e202414246
Lanthanide-tetrazine probes for bio-imaging and click chemistry.
Authors: Woolley, Benjamin and Wu, Yue and Xiong, Li and Chau, Ho-Fai and Zhang, Junhui and Law, Ga-Lai and Wong, Ka-Leung and Long, Nicholas J
Journal: Chemical science (2025)
Co-aggregation as A Simple Strategy for Preparing Fluorogenic Tetrazine Probes with On-Demand Fluorogen Selection.
Authors: Segawa, Shinsuke and Wu, Jiajie and Kwok, Ryan T K and Wong, Terence T W and He, Xuewen and Tang, Ben Zhong
Journal: Angewandte Chemie (International ed. in English) (2024): e202313930
Page updated on May 19, 2025

Ordering information

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Catalog Number2849
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Additional ordering information

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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.21

Correction Factor (280 nm)

0.08

Extinction coefficient (cm -1 M -1)

115,000

Excitation (nm)

510

Emission (nm)

531

Quantum yield

0.85

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
Product Image
Product Image
Gallery Image 1
Schematic illustrating the strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a tetrazine–dye conjugate and a trans‐cyclooctene (TCO)–modified biomolecule. The tetrazine–dye selectively and rapidly reacts with the TCO moiety on the biomolecule to form a stable linkage, labeling the nucleic acid with the dye. This bioorthogonal “click chemistry” process is fast, selective, and well‐suited for biocompatible labeling applications.