Rhodamine 110 chloride

CHF 64.00
In stock
CDX-R0016-M250250 mgCHF 64.00
CDX-R0016-G0011 gCHF 198.00
More Information
Product Details
Synonyms RH110; Rhodamine 560 Chloride; Rhodamine N; 3,6-Diamino-9-(2-carboxyphenyl)xanthylium chloride
Product Type Chemical
Properties
Formula C20H14N2O3 . HCl
MW 330.3 . 36.5
CAS 13558-31-1
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (HPLC)
Appearance Red to red-brown crystalline or powder.
Solubility Soluble in ethanol, methanol, DMSO or DMF. Slightly soluble in water.
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 JNGRENQDBKMCCR-UHFFFAOYSA-N
Smiles Cl.NC1=CC=C2C(OC3=CC(=N)C=CC3=C2C2=C(C=CC=C2)C(O)=O)=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°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 RT.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF

Fluorescent dye. Fluorophore standard that is widely used in enzyme assay systems. Precursor for a variety of R110-based enzyme substrates for flow cytometric measurements. Used as a calibration standard for R110-based enzyme substrates. Compared to AMC and AFC enzyme substrates, fluorogenic R110 substrates are generally more sensitive, giving longer absorption and fluorescence wavelength than AMC and AFC substrates. Spectral data: λex 498nm| λem 520nm in methanol.

Product References

(1) R.F. Kubin, & A.N. Fletcher; J. Luminesc. 27, 455 (1983) | (2) E. Koller; Appl. Fluoresc. Technol. 3, 20 (1991) | (3) S. Klingel, et al.; Methods Cell Biol. 41, 449 (1994) (Review) | (4) S. Ganesh, et al.; Cytometry 20, 334 (1995) | (5) H. Hug, et al.; Biochemistry 38, 13906 (1999) | (6) X. Zhang, et al.; Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 59A, 1667 (2003) | (7) H. Abe, et al.; Bioconjugate Chem. 19, 1219 (2008) | (8) R.W. Watkins, et al.; Org. Biomol. Chem. 7, 3969 (2009)

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