Coumarin 343 azide

This product is discontinued, and no longer available.
 We recommend AF 343 (Coumarin) X azide as a substitute

This product will be discontinued soon in favor of Coumarin 343 X azide. We may still have some material in stock (please see availability above).

This greenish-blue emitting fluorophore can be used as a FRET donor for FAM. Azide derivative is suitable for click chemistry.

Coumarin 343 absorption and emission spectra

Coumarin 343 absorption and emission spectra

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sulfo-Cyanine3 amine

Water soluble cyanine dye with bright fluorescence and high extinction coefficient. Contains an amino group for the conjugation with electrophiles and enzymatic transamination labeling.

Cyanine2 NHS ester minimal dye

Cyanine2 NHS ester minimal dye for protein labeling

BDP 630/650 X NHS ester

BDP 630/650 is a borondipyrromethene fluorophore tuned to Cyanine5 excitation and emission channels. The dye is bright and highly photostable. It is useful for fluorescence polarization assays. This is an amine-reactive NHS ester derivative.

General properties

Appearance: yellow powder
Molecular weight: 441.48
CAS number: 1807503-82-7
Molecular formula: C22H27N5O5
Solubility: Good in organic solvents (DCM, chloroform, DMF, DMSO, MeCN, alcohols), poor in water
Quality control: NMR 1H (95%) TLC, functional testing
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/absorption maximum, nm: 437
ε, L⋅mol−1⋅cm−1: 39000
Emission maximum, nm: 477
Fluorescence quantum yield: 0.63
CF260: 0.29
CF280: 0.24

Product citations

  1. Musiol-Kroll, E.M.; Zubeil, F.; Schafhauser, T.; Härtner, T.; Kulik, A.; McArthur, J.B.; Koryakina, I.; Wohlleben, W.; Grond, S.; Williams, G.J.; Lee, S.Y.; Weber, T. Polyketide bio-derivatization using the promiscuous acyltransferase KirCII. ACS Synthetic Biology, 2017, 6(3), 421–427. doi: 10.1021/acssynbio.6b00341
  2. Teske, N.S.; Voigt, J.; Shastri, V.P. Clickable Degradable Aliphatic Polyesters via Copolymerization with Alkyne Epoxy Esters: Synthesis and Postfunctionalization with Organic Dyes. Journal of the American Chemical Society, 2014, 136(29), 10527-10533. doi: 10.1021/ja505629w
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