sulfo-Cyanine3 amine

Amines sulfo-Cyanine3

Cat. #	Quantity	Price	Lead time
113C0	1 mg	$115	in stock
213C0	5 mg	$285	in stock
413C0	25 mg	$680	in stock
513C0	50 mg	$1270	in stock
613C0	100 mg	$1990	in stock

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A water-soluble dye with an amino group that is useful for the conjugation with electrophiles and for enzymatic transamination labeling.

sulfo-Cyanine3 is a sulfonated analog of Cy3®, which is compatible with various fluorescence measuring equipment. The dye is highly photostable. It is also easily detectable by the naked eye.

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Sulfo-Cy3 absorbance and emission spectra

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Cyanine3 azide

Azide derivative of Cyanine3 fluorescent dye for сlick сhemistry.

BDP 630/650 is a bright fluorophore for far red part of the spectrum. This dye is perfect for microscopy and fluorescence polarization assays. This is a carboxylic acid that can be activated for the coupling, or used as a control.

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AF 488 azide

AF 488 azide is a fluorophore with emission in the green spectrum range. It reacts with alkynes in copper-catalyzed cycloaddition reactions.

General properties

Appearance:	dark red solid
Molecular weight:	714.94
CAS number:	2183440-43-7
Molecular formula:	C₃₆H₅₀N₄O₇S₂
IUPAC name:	3H-Indolium, 1-[6-[(6-aminohexyl)amino]-6-oxohexyl]-2-[3-(1,3-dihydro-1,3,3-trimethyl-5-sulfo-2H-indol-2-ylidene)-1-propen-1-yl]-3,3-dimethyl-5-sulfo-, inner salt
Solubility:	well soluble in water (0.49 M = 350 g/L), alcohols, DMSO, DMF
Quality control:	NMR ¹H, HPLC-MS (95%)
Storage conditions:	Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate.
MSDS:	Download
	Product specifications

Spectral properties

Excitation/absorption maximum, nm:	548
ε, L⋅mol⁻¹⋅cm⁻¹:	162000
Emission maximum, nm:	563
Fluorescence quantum yield:	0.1
CF₂₆₀:	0.03
CF₂₈₀:	0.06

Product citations

Henry, W.S.; Müller, S.; Yang, J.-S.; Innes-Gold, S.; Das, S.; Reinhardt, F.; Sigmund, K.; Phadnis, V.V.; Wan, Z.; Eaton, E.; Sampaio, J.L.; Bell, G.W.; Viravalli, A.; Hammond, P.T.; Kamm, R.D.; Cohen, A.E.; Boehnke, N.; Hsu, V.W.; Levental, K.R.; Rodriguez, R.; Weinberg, R.A. Ether lipids influence cancer cell fate by modulating iron uptake. bioRxiv, 2024, preprint. doi: 10.1101/2024.03.20.585922
Bos, I.; Timmerman, M.; Sprakel, J. FRET-Based Determination of the Exchange Dynamics of Complex Coacervate Core Micelles. Macromolecules, 2021, 54(1), 398–411. doi: 10.1021/acs.macromol.0c02387
Zhang, Q.; Scigliano, A.; Biver, T.; Pucci, A.; Swager, T.M. Interfacial Bioconjugation on Emulsion Droplet for Biosensors. Bioorganic & Medicinal Chemistry, 2018, 26(19), 5307–5313. doi: 10.1016/j.bmc.2018.04.020
Sobotzki, N.; Schafroth, M.A.; Rudnicka, A.; Koetemann, A.; Marty, F.; Goetze, S.; Yamauchi, Y.; Carreira, E.M.; Wollscheid, B. HATRIC-based identification of receptors for orphan ligands. Nature Communications, 2018, 9, 1519. doi: 10.1038/s41467-018-03936-z

This Product is offered and sold for research purposes only. It has not been tested for safety and efficacy in food, drug, medical device, cosmetic, commercial or any other use. Supply does not express or imply authorization to use for any other purpose, including, without limitation, in vitro diagnostic purposes, in the manufacture of food or pharmaceutical products, in medical devices or in cosmetic products.