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iFluor® 594 amine

Product key features

  • Ex/Em: 587/603 nm
  • Extinction coefficient: 200,000 cm-1M-1
  • Reactive Group: Amine
  • Versatile Conjugation: Efficiently labels carboxyl groups and also serves as an amine donor for enzymatic transamination labeling
  • High Photostability & Brightness – Delivers strong fluorescence signals with minimal photobleaching, ideal for imaging and flow cytometry applications.
  • Broad pH Stability – Maintains consistent fluorescence across a wide pH range (pH 3–11), enabling use in diverse biological environments.

Product description

iFluor® 594 amine is a bright, red-fluorescent dye functionalized with a primary amine group for covalent conjugation to activated carboxyl groups. It is engineered for high-efficiency labeling via carbodiimide-mediated coupling reactions, such as EDC/NHS activation, resulting in the formation of stable amide linkages. The dye exhibits excitation and emission maxima at approximately 588 nm and 604 nm, respectively, with spectral properties comparable to Texas Red® and Alexa Fluor® 594, enabling seamless integration into existing fluorescence-based workflows. iFluor® 594 demonstrates excellent photostability, high quantum yield, and pH-independent fluorescence across a broad range (pH 3–11), making it suitable for a wide range of applications including fluorescence microscopy, flow cytometry, and high-throughput screening.

In addition to conventional coupling strategies, the primary amine of iFluor® 594 is compatible with enzymatic transamination reactions, facilitating site-specific protein labeling under mild, physiologically relevant conditions. When used to generate tandem conjugates with donor proteins such as R-phycoerythrin (PE), iFluor® 594 significantly enhances FRET efficiency and reduces spectral crosstalk compared to traditional PE–Texas Red® conjugates. These attributes make iFluor® 594 amine a robust and versatile fluorophore for the development of advanced probes in complex, multicolor analytical and imaging assays.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
iFluor® 350 amine3454502000010.9510.830.23
iFluor® 405 amine4034273700010.9110.480.77
iFluor® 488 amine4915167500010.910.210.11
iFluor® 555 amine55757010000010.6410.230.14
iFluor® 594 Styramide *Superior Replacement for Alexa Fluor 594 tyramide*58760320000010.5310.050.04
iFluor® 594 TCO58760320000010.5310.050.04
iFluor® 594 Tetrazine58760320000010.5310.050.04
iFluor® 647 amine65667025000010.2510.030.03
iFluor® 660 amine66367825000010.2610.070.08
iFluor® 680 amine68470122000010.2310.0970.094
iFluor® 700 amine69071322000010.2310.090.04
iFluor® 710 amine71673915000010.6010.120.07
iFluor® 750 amine75777927500010.1210.0440.039
iFluor® 790 amine78781225000010.1310.10.09
Show More (5)

References

View all 50 references: Citation Explorer
Na-Ag Ion-Exchanged Glass Substrates for Plasmon-Enhanced Fluorescence Imaging of Neutrophils.
Authors: Inozemtsev, Vladimir A and Dokukin, Maxim E and Sgibnev, Yevgeniy M and Sherstyukova, Ekaterina A and Kandrashina, Snezhanna S and Shvedov, Mikhail A and Shelaev, Artem V and Nikonorov, Nikolay V and Sergunova, Viktoria A and Baryshev, Alexander V
Journal: Sensors (Basel, Switzerland) (2025)
Correlative super-resolution microscopy with deep UV reactivation.
Authors: Prakash, Kirti
Journal: Journal of microscopy (2023)
Amphiphilic Poly(2-oxazoline)s with Glycine-Containing Hydrophobic Blocks Tailored for Panobinostat- and Imatinib-Loaded Micelles.
Authors: Göppert, Natalie E and Quader, Sabina and Van Guyse, Joachim F R and Weber, Christine and Kataoka, Kazunori and Schubert, Ulrich S
Journal: Biomacromolecules (2023): 5915-5925
Anatomical analyses of collateral prefrontal cortex projections to the basolateral amygdala and the nucleus accumbens core in rats.
Authors: Shih, Cheng-Wei and Chang, Chun-Hui
Journal: Brain structure & function (2023)
A model eye for fluorescent characterization of retinal cultures and tissues.
Authors: Ferraro, G and Gigante, Y and Pitea, M and Mautone, L and Ruocco, G and Di Angelantonio, S and Leonetti, M
Journal: Scientific reports (2023): 10983
Page updated on June 29, 2025

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Catalog Number1089
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Physical properties

Molecular weight

1017.08

Solvent

DMSO

Spectral properties

Absorbance (nm)

587

Correction Factor (260 nm)

0.05

Correction Factor (280 nm)

0.04

Extinction coefficient (cm -1 M -1)

2000001

Excitation (nm)

587

Emission (nm)

603

Quantum yield

0.531

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 representation of carbodiimide-mediated coupling between an amine-functionalized dye and a carboxylated biomolecule. Reagents like EDC activate carboxyl groups to form reactive intermediates that react with primary amines, forming stable amide bonds. This approach enables efficient covalent labeling of peptides, proteins, and nucleic acids for bioanalytical applications
Schematic representation of carbodiimide-mediated coupling between an amine-functionalized dye and a carboxylated biomolecule. Reagents like EDC activate carboxyl groups to form reactive intermediates that react with primary amines, forming stable amide bonds. This approach enables efficient covalent labeling of peptides, proteins, and nucleic acids for bioanalytical applications
Schematic representation of carbodiimide-mediated coupling between an amine-functionalized dye and a carboxylated biomolecule. Reagents like EDC activate carboxyl groups to form reactive intermediates that react with primary amines, forming stable amide bonds. This approach enables efficient covalent labeling of peptides, proteins, and nucleic acids for bioanalytical applications