Rhodamine 6G

CHF 23.00
In stock
CDX-R0032-G02525 gCHF 23.00
CDX-R0032-G100100 gCHF 70.00
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Product Details
Synonyms 6-Carboxyrhodamine; Aizen Rhodamine 6GCP; Basic Red 1; C.I. 45160; Calcozine Red 6G; NSC 36345
Product Type Chemical
Properties
Formula C28H30N2O3 . HCl
MW 442.5 . 36.5
CAS 989-38-8
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (TLC)
Appearance Greenish red powder.
Solubility Soluble in methanol, water or ethanol.
Identity Determined by NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key VYXSBFYARXAAKO-WTKGSRSZSA-N
Smiles Cl.CCNC1=C(C)C=C2C(OC3=C\C(=N/CC)C(C)=CC3=C2C2=C(C=CC=C2)C(=O)OCC)=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Keep cool and dry.
Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF

Rhodamine 6G is a highly fluorescent hydrophilic pH-sensitive dye. It is often used as a tracer dye within water to determine the rate and direction of flow and transport. Rhodamine dyes are used extensively in biotechnology applications such as fluorescence microscopy, flow cytometry, fluorescence correlation spectroscopy and ELISA. The dye has a remarkably high photostability and high fluorescence quantum yield. Used as a laser dye and potential mitochondrial probe. The lasing range of the dye is 555 to 585 nm with a maximum at 566 nm. Useful in Pgp efflux assays and has been used to characterize kinetics of MRP1-mediated efflux. Spectral data: λex 528 nm| λem 551 nm (in MeOH).

Product References

(1) T. Aiuchi, et al.; Biochim. Biophys. Acta. 685, 289 (1982) | (2) R.F. Kubin & A.N. Fletcher; J. Luminesc. 27, 455 (1983) | (3) M.W. Berns, et al.; Cell Biophys. 6, 263 (1984) | (4) Y. Matsumoto, et al.; J. Neurooncol. 13, 217 (1992) | (5) M. Mandala, et al.; Anal. Biochem. 274, 1 (1999) | (6) D. Magde, et al.; Photochem. Photobiol. 75, 327 (2002) | (7) Z. Chen, et al.; J. Fluoresc. 18, 93 (2008) | (8) T. Baumgartel, et al.; Nanotechnology 21, 475205 (2010)

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