Cyanine5 amine

Cat. # Quantity Price Lead time
130C0 1 mg $110.00 in stock
230C0 5 mg $210.00 in stock
430C0 25 mg $410.00 in stock
530C0 50 mg $695.00 in stock
630C0 100 mg $1190.00 in stock

Cyanine5 amine is a reactive dye which contains amino group, an analog of Cy5® amine. This reagent can be coupled with a variety of activated esters and other electrophilic reagents. For example, this amine can be coupled with EDC-activated carboxylic groups.

This bright and photostable dye is suitable for many different methods of fluorescence detection. Colorful fluorophore can also be easily detected in small quantities (nanomols) by naked human eye.

Cyanine5 amine absorbance and emission spectra

Cyanine5 amine absorbance and emission spectra

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General properties

Appearance: dark blue powder
Molecular weight: 653.77
CAS number: 1807529-70-9
Molecular formula: C38H54Cl2N4O
IUPAC name: 3H-​Indolium, 2-​[5-​[1-​[6-​[(6-​aminohexyl)​amino]​-​6-​oxohexyl]​-​1,​3-​dihydro-​3,​3-​dimethyl-​2H-​indol-​2-​ylidene]​-​1,​3-​pentadien-​1-​yl]​-​1,​3,​3-​trimethyl-
Solubility: moderate solubility in water, good in polar organic solvents (DMF, DMSO, alcohols)
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.
MSDS: Download
Product specifications

Spectral properties

Excitation maximum, nm: 646
ε, L⋅mol−1⋅cm−1: 250000
Emission maximum, nm: 662
Fluorescence quantum yield: 0.2
CF260: 0.03
CF280: 0.04

Product citations

  1. Kántor, I.; Aparaschivei, D.; Todea, A.; Biró, E.; Babos, G.; Szerényi, D.; Kakasi, B.; Péter, F:; Şişu, Eugen and Feczkó, T. Biocatalytic synthesis of poly[ε-caprolactone-co-(12-hydroxystearate)] copolymer for sorafenib nanoformulation useful in drug delivery. Catalysis Today, in press. doi: 10.1016/j.cattod.2020.05.005
  2. McCrorie, P.; Mistry, J.; Taresco, V.; Lovato, T.; Fay, M.; Ward, I.; Ritchie, A.A.; Clarke, P.A.; Smith, S.J.; Marlow, M.; Rahman, R. Etoposide and olaparib polymer-coated nanoparticles within a bioadhesive sprayable hydrogel for post-surgical localised delivery to brain tumours. European Journal of Pharmaceutics and Biopharmaceutics, 2020, 157, 108–120. doi: 10.1016/j.ejpb.2020.10.005
  3. Hortelão, Ana C. and García-Jimeno, S.; Cano-Sarabia, M.; Patiño, T.; Maspoch, D.; Sanchez, S. LipoBots: Using Liposomal Vesicles as Protective Shell of Urease-Based Nanomotors. Advanced Functional Materials, 2020, 30(42), 2002767. doi: 10.1002/adfm.202002767
  4. Mahmoud, A.M.; Morrow, J.P.; Pizzi, D.; Azizah, A.M.; Davis, T.P.; Tabor, R.F.; Kempe, K. Tuning Cellular Interactions of Carboxylic Acid Side Chain Containing Polyacrylates: The Role of Cyanine Dye Label and Side Chain Type. Biomacromolecules, 2020, 21(8), 3007–3016. doi: 10.1021/acs.biomac.0c00244
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