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ATTO 514 alkyne

Product key features

  • Ex/Em: 510/531 nm
  • Extinction coefficient: 115,000 cm-1M-1
  • Reactive group: alkyne
  • Efficient Conjugation: Click chemistry labeling of azides on peptides, antibodies, and other 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 alkyne is manufactured by AAT Bioquest for research and development use. ATTO 514 alkyne is widely used for labeling azides on peptides, antibodies, and other biomolecules via click chemistry with the bright, green fluorescent ATTO 514 dye. It participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with azide-containing molecules.

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 alkyne39047524000.900.460.09
ATTO 425 alkyne438484450000.900.190.17
ATTO 488 alkyne499520900000.800.220.09
ATTO 495 alkyne497525800000.20.450.37
ATTO 514 TCO510531115,0000.850.210.08
ATTO 514 Tetrazine510531115,0000.850.210.08
ATTO 532 alkyne5315521150000.900.220.11
ATTO 550 alkyne5535741200000.800.230.10
ATTO 565 alkyne5625891200000.900.270.12
ATTO 590 alkyne5926211200000.800.390.43
ATTO 594 alkyne6026211200000.850.260.51
ATTO 610 alkyne6156321500000.700.030.06
ATTO 620 alkyne61964112000010.510.040.06
ATTO 633 alkyne6296511300000.6410.040.05
ATTO 647N alkyne6456631500000.6510.060.05
ATTO 655 alkyne6616791250000.310.240.08
ATTO 680 alkyne6796961250000.300.300.17
ATTO 700 alkyne6997151200000.250.260.41
Show More (9)

References

View all 50 references: Citation Explorer
Utilizing Alkyne-Nitrone Cycloaddition for the Convenient Multi-Component Assembly of Protein Degraders and Biological Probes.
Authors: Lin, Shiou-Ting and Wang, Chien-Hua and Chen, Ai-Lin and Andrew Wang, Tsung-Shing
Journal: Chemistry (Weinheim an der Bergstrasse, Germany) (2025): e202403184
Piezoelectrostatic Catalysis of the Azide-Alkyne Huisgen Cycloaddition.
Authors: Tang, Qiao and Sanchis-Gual, Roger and Qin, Ni and Ye, Hao and Sevim, Semih and Veciana, Andrea and Corral-Casas, Carlos and Thodkar, Kishan and Wu, Jiang and Nelson, Bradley J and Díez-Pérez, Ismael and Chen, Xiang-Zhong and Gattinoni, Chiara and Puigmartí-Luis, Josep and Pané, Salvador and Franco, Carlos
Journal: Journal of the American Chemical Society (2025): 8289-8299
Multicomponent Reaction Integrating Selenium(II)-Nitrogen Exchange (SeNEx) Chemistry and Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC).
Authors: Hou, Wei and Zhou, Xiaohui and Yang, Zhikun and Xia, Huhui and Wang, Yan and Xu, Keren and Hou, Shaoneng and Zhang, Shuning and Cui, Dongmei and Ma, Peixiang and Zhou, Wei and Xu, Hongtao
Journal: Angewandte Chemie (International ed. in English) (2025): e202500942
Enantioselective Synthesis of Inherently Chiral Pillar[5]Arenes Through Copper-Catalyzed Azide-Alkyne Cycloaddition.
Authors: Zhou, Wen-Guang and Xi, Long-Long and Zhang, Mei-Ru and Wang, Hao-Ran and An, Mei and Li, Jia-Hao and Liu, Ren-Rong
Journal: Angewandte Chemie (International ed. in English) (2025): e202502381
Combination of atom transfer radical polymerization and alkyne-azide click-chemistry for the synthesis of phosphonic acid cation exchange materials.
Authors: Schipplick, Luca and Kahler, Philipp and Seubert, Andreas
Journal: Journal of chromatography. A (2025): 465675
Page updated on May 19, 2025

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Catalog Number2846
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Physical properties

Molecular weight

891.90

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 azide–alkyne cycloaddition (“click chemistry”) between an alkyne‐functionalized dye and an azide‐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, tolerates a wide range of functional groups, and is frequently used to label proteins, nucleic acids, and other biomolecules for imaging, proteomics, and high‐throughput assays.