TAMRA alkyne, 5-isomer

Alkynes TAMRA (TMR, Tetramethylrhodamine) Click chemistry
Cat. # Quantity Price Lead time
A71B0 1 mg –   in stock
B71B0 5 mg $260 in stock
C71B0 10 mg $325 in stock
D71B0 25 mg $410 in stock
E71B0 50 mg $695 in stock
F71B0 100 mg $890 in stock
Sample request
Found better price? Let us know and we will propose the way forward!

TAMRA alkyne for click chemistry, pure 5-isomer. TAMRA (TMR, tetramethylrhodamine) is a xanthene dye. It forms a FRET pair with fluorescein.

This alkyne is suitable for сopper-catalyzed сlick chemistry (CuAAC).

TAMRA alkyne, 5-isomer, E71B0
TAMRA alkyne, 5-isomer, E71B0
TAMRA alkyne, 5-isomer, E71B0
Structure of TAMRA alkyne, 5-isomer
Download in
ChemDraw format

Absorption and emission spectra of 5-TAMRA

Absorption and emission spectra of 5-TAMRA

Recommended protocol

Calculator

Customers also purchased with this product

TAMRA alkyne, 6-isomer

Terminal alkyne for copper-catalyzed click chemistry. Tetramethylrhodamine (TAMRA) is a rhodamine dye which is popular in qPCR and other applications. TAMRA is a also a FRET acceptor for FAM.

Cyanine3 alkyne

Cyanine3 alkyne is a fluorescent dye alkyne for сlick сhemistry.

Cyanine5.5 alkyne

Cyanine5.5 alkyne is a NIR (near infrared) dye azide for copper-catalyzed сlick сhemistry.
Add this product to your cart and
get free express delivery

General properties

Appearance: violet solid
Mass spec M+ increment: 467.2
Molecular weight: 467.51
CAS number: 945928-17-6
Molecular formula: C28H25N3O4
Solubility: good in DMF, DMSO, low 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.
MSDS: Download
Product specifications

Spectral properties

Excitation/absorption maximum, nm: 541
ε, L⋅mol−1⋅cm−1: 84000
Emission maximum, nm: 567
Fluorescence quantum yield: 0.1
CF260: 0.32
CF280: 0.19

Product citations

  1. Guarin, M.; Faelens, R.; Giusti, A.; De Croze, N.; Léonard, M.; Cabooter, D.; Annaert, P.; de Witte, P.; Ny, A. Spatiotemporal Imaging and Pharmacokinetic of Fluorescent Compounds in Zebrafish Eleuthero-Embryos After Different Routes of Administration. Scientific Reports, 2021, 11(1), 12229. doi: 10.1038/s41598-021-91612-6.
  2. Guarin, M.; Ny, A.; De Croze, N.; Maes, J.; Léonard, M.; Annaert, P.; de Witte, P. A. M. Pharmacokinetics in Zebrafish Embryos (ZFE) Following Immersion and Intrayolk Administration: A Fluorescence-Based Analysis. Pharmaceuticals, 2021, 14(6), 576. doi: 10.3390/ph14060576
  3. Guarin, M.; Faelens, R.; Giusti, A.; De Croze, N.; Léonard, M.; Cabooter, D.; Annaert, P.; de Witte, P.; Ny, A. Spatiotemporal imaging and pharmacokinetics of fluorescent compounds in zebrafish eleuthero-embryos after different routes of administration. Scientific Reports, 2021, 11, 12229. doi: 10.1038/s41598-021-91612-6
  4. Rojas-Sánchez, L.; Sokolova, V.; Riebe, S.; Voskuhl, J.; Epple, M. Covalent Surface Functionalization of Calcium Phosphate Nanoparticles with Fluorescent Dyes by Copper-Catalysed and by Strain-Promoted Azide-Alkyne Click Chemistry. ChemNanoMat, 2019, 5(4), 436–446. doi: 10.1002/cnma.201800509
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.
Short link - lumiprobe.com/sh/p/24
Your item has been added. View your cart or proceed to checkout
The count of items is incorrect.