logo
AAT Bioquest

ATTO 425 azide

Product key features

  • Ex/Em: 438/484 nm
  • Extinction coefficient: 45,000 cm-1M-1
  • Reactive group: azide
  • Precise Conjugation: Readily and selectively labels alkyne targets via click chemistry
  • High Quantum Yield & Photostability: Delivers strong, stable fluorescence for sensitive applications
  • Enhanced Signal Separation: Minimal excitation and emission overlap reduces background interference

Product description

ATTO 425 azide is manufactured by AAT Bioquest for research and development use. ATTO 425 is a coumarin-based fluorescent dye characterized by its high fluorescence quantum yield, large Stokes shift, excellent photostability, and low molecular weight. It exhibits moderate hydrophilicity and is optimally excited in the 405-455 nm wavelength range. These properties make ATTO 425 particularly suitable for applications in single-molecule detection and high-resolution microscopy techniques, including PALM, dSTORM, and STED microscopy. Additionally, ATTO 425 is well-suited for use in flow cytometry (FACS), fluorescence in situ hybridization (FISH), and various other biological assays.

The azide derivative of ATTO 425 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

References

View all 4 references: Citation Explorer
Ratiometric Fluorescent Biosensor Based on Self-Assembled Fluorescent Gold Nanoparticles and Duplex-Specific Nuclease-Assisted Signal Amplification for Sensitive Detection of Exosomal miRNA.
Authors: Sun, Zhiwei and Li, Juan and Yang, Yufei and Tong, Yao and Li, Hui and Wang, Chuanxin and Du, Lutao and Jiang, Yanyan
Journal: Bioconjugate chemistry (2022): 1698-1706
Ratiometric Fluorescence Detection of Colorectal Cancer-Associated Exosomal miR-92a-3p with DSN-Assisted Signal Amplification by a MWCNTs@Au NCs Nanoplatform.
Authors: Sun, Zhiwei and Li, Juan and Tong, Yao and Zhao, Li and Zhou, Xiaoyu and Li, Hui and Wang, Chuanxin and Du, Lutao and Jiang, Yanyan
Journal: Biosensors (2022)
Avidin/Biotin Bioinspired Platform for Dual In Vivo 18F-PET/NIRF Molecular Imaging.
Authors: Damont, Annelaure and Boisgard, Raphael and Dollé, Frédéric and Hollocou, Morgane and Kuhnast, Bertrand
Journal: Bioconjugate chemistry (2017): 2524-2529
Fluorescence of dyes in solutions with high absorbance. Inner filter effect correction.
Authors: Fonin, Alexander V and Sulatskaya, Anna I and Kuznetsova, Irina M and Turoverov, Konstantin K
Journal: PloS one (2014): e103878
Page updated on May 19, 2025

Ordering information

Price
Unit size
Catalog Number70213
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

Molecular weight

601.70

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.19

Correction Factor (280 nm)

0.17

Extinction coefficient (cm -1 M -1)

45000

Excitation (nm)

438

Emission (nm)

484

Quantum yield

0.90

Storage, safety and handling

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

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12352200
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.
Gallery Image 2