BDP® FL alkyne

Cat. # Quantity Price Lead time
A14B0 1 mg $125 in stock
B14B0 5 mg $260 in stock
C14B0 10 mg $325 in stock
D14B0 25 mg $510 in stock
E14B0 50 mg $895 in stock
F14B0 100 mg $1490 in stock
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Alkyne derivative of BDP FL. BDP FL is a borondipyrromethene dye, a bright and photostable fluorophore which emits in fluorescein (FAM) channel. Unlike FAM, BDP FL is very photostable. Its brightness is similar to fluorescein.

This alkyne can be conjugated with a number of azide-containing molecules by copper-catalyzed click chemistry.

BDP FL absorption and emission spectra

BDP FL absorption and emission spectra

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BDP® FL NHS ester

Amino-reactive BDP FL, a very bright and photostable dye for fluorescein channel.
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BDP® TMR NHS ester

Amine reactive NHS ester of BDP TMR, bright borondipyrromethene dye for TAMRA channel especially suitable for fluorescence polarization assays.

General properties

Appearance: orange solid
Mass spec M+ increment: 329.1
Molecular weight: 329.15
CAS number: 302795-84-2, 2006345-30-6
Molecular formula: C17H18BF2N3O
Solubility: Good in organic solvents (DMF, DMSO, dichlromethane), limited in water
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: 503
ε, L⋅mol−1⋅cm−1: 92000
Emission maximum, nm: 509
Fluorescence quantum yield: 0.97
CF260: 0.015
CF280: 0.027

Product citations

  1. Fong, C.K.; Andersen, M.J.; Kunesh, E.; Leonard, E.; Durand, D.; Coombs, R.; Flores-Mireles, A.L.; Howell, C. Removal of Free Liquid Layer from Liquid-Infused Catheters Reduces Silicone Loss into the Environment while Maintaining Adhesion Resistance. medRxiv, 2023, preprint. doi: 10.1101/2023.09.14.23295548
  2. Charoen-Rajapark, P.; Clarke, D.R. Confocal microscopy observations of electrical pre-breakdown of bi-layer elastomer dielectrics. Extreme Mechanics Letters, 2021, 49, 101473. doi: 10.1016/j.eml.2021.101473
  3. Abukar, T.; Rahmani, S.; Thompson, N.K.; Antonescu, C.N.; Wakarchuk, W.W. Development of BODIPY labelled sialic acids as sialyltransferase substrates for direct detection of terminal galactose on N- and O-linked glycans. Carbohydrate Research, 2021, 500, 108249. doi: 10.1016/j.carres.2021.108249
  4. Merlo, R.; Caprioglio, D.; Cillo, M.; Valenti, A.; Mattossovich, R.; Morrone, C.; Massarotti, A.; Rossi, F.; Miggiano, R.; Leonardi, A.; Minassi, A.; Perugino, G. The SNAP-tag technology revised: an effective chemo-enzymatic approach by using a universal azide-based substrate. Journal of Enzyme Inhibition and Medicinal Chemistry, 2021, 36(1), 85–97. doi: 10.1080/14756366.2020.1841182
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