logo
AAT Bioquest

ATTO 532 PEG4 DBCO

Product key features

  • Ex/Em: 531/552 nm
  • Extinction coefficient: 115,000 cm-1M-1
  • Reactive group: DBCO
  • Click Chemistry: enables copper-free, bioorthogonal labeling of azide-functionalized biomolecules
  • High Quantum Yield & Photostability: ensures intense fluorescence signals for reliable detection and imaging
  • Excellent Hydrophilicity: Prevents aggregation and enhances signal clarity in live-cell applications
  • Advanced Imaging Performance: Suitable for single-molecule detection and super-resolution techniques, including SIM and STED

Product description

ATTO 532 PEG4 DBCO is manufactured by AAT Bioquest for research and development use. ATTO 532 is a rhodamine-based fluorescent dye notable for its high molar absorptivity and fluorescence quantum yield (0.90), providing robust signal intensity in fluorescence applications. Its combination of photostability, aqueous solubility, and sufficient Stokes shift makes it suitable for single-molecule detection and high-resolution microscopy techniques, including SIM and STED microscopy. ATTO 532 is also effective in flow cytometry, FISH, and a variety of biological assays, offering flexibility for diverse fluorescence-based experimental protocols. The dye is optimally excited within the 515-545 nm range, with a frequency-doubled Nd:YAG laser at 532 nm serving as an ideal excitation source.

The DBCO derivative of ATTO 532 is a highly reactive cycloalkyne optimized for copper-free click chemistry (SPAAC, strain-promoted azide-alkyne cycloaddition). This derivative exhibits a significantly higher reaction rate with azides compared to other cyclooctynes and copper-catalyzed click reactions (CuAAC). Uniquely, DBCO does not react with tetrazines, allowing for its use in bioorthogonal reactions alongside trans-cyclooctenes and tetrazines. For applications where the presence of copper is problematic, ATTO 532 DBCO serves as an effective alternative to copper-dependent fluorescent alkynes.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 514 PEG4 DBCO510531115,0000.850.210.08
ATTO 594 PEG4 DBCO6026211200000.850.260.51
ATTO 647 PEG4 DBCO6466661200000.200.080.04
ATTO 647N PEG4 DBCO6456631500000.6510.060.05
ATTO 655 PEG4 DBCO6616791250000.310.240.08
ATTO 680 PEG4 DBCO6796961250000.300.300.17
ATTO 700 PEG4 DBCO6997151200000.250.260.41

References

View all 4 references: Citation Explorer
Extending the Palette of Green Coumarin Photocages - Oligonucleotide Fragmentation and Superior 5'-Caps.
Authors: Kaufmann, Janik and Wolf, Jonas and Heckel, Alexander
Journal: Chemistry (Weinheim an der Bergstrasse, Germany) (2023): e202300390
DNA-Programmed Lipid Nanoreactors for Synthesis of Carbohydrate Mimetics by Fusion of Aqueous Sub-attoliter Compartments.
Authors: Tian, Xinwei and Risgaard, Nikolaj Alexander and Löffler, Philipp M G and Vogel, Stefan
Journal: Journal of the American Chemical Society (2023)
Click chemistry for the conservation of cellular structures and fluorescent proteins: ClickOx.
Authors: Löschberger, Anna and Niehörster, Thomas and Sauer, Markus
Journal: Biotechnology journal (2014): 693-7
Clickable degradable aliphatic polyesters via copolymerization with alkyne epoxy esters: synthesis and postfunctionalization with organic dyes.
Authors: Teske, Nele S and Voigt, Julia and Shastri, V Prasad
Journal: Journal of the American Chemical Society (2014): 10527-33
Page updated on May 19, 2025

Ordering information

Price
Unit size
Catalog Number2821
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

1189.40

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.22

Correction Factor (280 nm)

0.11

Extinction coefficient (cm -1 M -1)

115000

Excitation (nm)

531

Emission (nm)

552

Quantum yield

0.90

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
UNSPSC12352200
Product Image
Product Image
Gallery Image 1
Schematic illustrating the strain‐promoted azide–alkyne cycloaddition (SPAAC) between a dibenzocyclooctyne (DBCO)–dye conjugate and an azide‐modified biomolecule. The DBCO’s ring strain drives the copper‐free reaction with the azide to form a stable 1,2,3-triazole linkage, avoiding potential toxicity of copper catalysts. This bioorthogonal labeling strategy proceeds efficiently under mild conditions, making it especially valuable for live‐cell imaging, in vivo studies, and other sensitive bioconjugation applications.