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In California, Rhodamine B is suspected to be carcinogenic and thus products containing it must contain a warning on its label.<ref>[http://www.brown.edu/Departments/Visual_Art/documents/NavalJelly.pdf Naval Jelly msds with Rhodamine B]</ref>
In California, Rhodamine B is suspected to be carcinogenic and thus products containing it must contain a warning on its label.<ref>[http://www.brown.edu/Departments/Visual_Art/documents/NavalJelly.pdf Naval Jelly msds with Rhodamine B]</ref>


In New Jersey, MSDS files state that there is limited evidence of carcinogenicity in laboratory animal, and no evidence at all in humans.<ref>[http://www.jtbaker.com/msds/englishhtml/r5400.htm J.T. Baker Rhodamine B MSDS]</ref>
In New Jersey, MSDS files state that there is limited evidence of carcinogenicity in laboratory animal, and no evidence at all in humans.<ref>[http://hazard.com/msds/mf/baker/baker/files/r5400.htm J.T. Baker Rhodamine B MSDS]</ref>


==References==
==References==

Revision as of 12:18, 31 July 2011

Rhodamine B
Names
IUPAC name
[9-(2-carboxyphenyl)-6-diethylamino-3-xanthenylidene]-diethylammonium chloride
Other names
Rhodamine 610, C.I. Pigment Violet 1, Basic Violet 10, C.I. 45170
Identifiers
3D model (JSmol)
ECHA InfoCard 100.001.259 Edit this at Wikidata
KEGG
  • CCN(CC)C1=CC2=C(C=C1)C(=C3C=CC(=[N+](CC)CC)C=C3O2)C4=CC=CC=C4C(=O)O.[Cl-]
Properties
C28H31ClN2O3
Molar mass 479.02
Appearance red to violet powder
Melting point 210 - 211 °C (Decomposes)
~50 g/L
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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An example of Beer–Lambert law, a green laser lighting in a solution of Rhodamine 6B, the beam becomes weaker as it progresses inward

Rhodamine B (Template:Pron-en) is a chemical compound and a dye. It is often used as a tracer dye within water to determine the rate and direction of flow and transport. Rhodamine dyes fluoresce and can thus be detected easily and inexpensively with instruments called fluorometers. Rhodamine dyes are used extensively in biotechnology applications such as fluorescence microscopy, flow cytometry, fluorescence correlation spectroscopy and ELISA.

Rhodamine B is used in biology as a staining fluorescent dye, sometimes in combination with auramine O, as the auramine-rhodamine stain to demonstrate acid-fast organisms, notably Mycobacterium.

Rhodamine B is tunable around 610 nm when used as a laser dye [1]. Its luminescence quantum yield is 0.65 in basic ethanol[2], 0.49 in ethanol [3], 1.0 [4], and 0.68 in 94% ethanol [5]. The fluorescence yield is temperature dependent.[6]

Solubility

The solubility of Rhodamine B in water is ~50 g/L. However, the solubility in acetic acid solution (30 vol.%) is ~400 g/L. Chlorinated tap water decomposes rhodamine B. Rhodamine B solutions adsorb to plastics and should be kept in glass [7].

Other uses

Rhodamine B is being tested for use as a biomarker in oral rabies vaccines for wildlife, such as raccoons, to identify animals that have eaten a vaccine bait. The rhodamine is incorporated into the animal's whiskers and teeth. [8]

It is also often mixed with herbicides to show where they have been used.

Safety and health

In California, Rhodamine B is suspected to be carcinogenic and thus products containing it must contain a warning on its label.[9]

In New Jersey, MSDS files state that there is limited evidence of carcinogenicity in laboratory animal, and no evidence at all in humans.[10]

References

  1. ^ Rhodamine B
  2. ^ Kubin, R (1983). "Fluorescence quantum yields of some rhodamine dyes". Journal of Luminescence. 27 (4): 455–462. doi:10.1016/0022-2313(82)90045-X.
  3. ^ Casey, Kelly G.; Quitevis, Edward L. (1988). "Effect of solvent polarity on nonradiative processes in xanthene dyes: Rhodamine B in normal alcohols". The Journal of Physical Chemistry. 92 (23): 6590–6594. doi:10.1021/j100334a023.
  4. ^ Kellogg, R. E.; Bennett, R. G. (1964). "Radiationless Intermolecular Energy Transfer. III. Determination of Phosphorescence Efficiencies". The Journal of Chemical Physics. 41 (10): 3042. doi:10.1063/1.1725672.
  5. ^ Snare, M (1982). "The photophysics of rhodamine B". Journal of Photochemistry. 18 (4): 335–346. doi:10.1016/0047-2670(82)87023-8.
  6. ^ Karstens, T.; Kobs, K. (1980). "Rhodamine B and rhodamine 101 as reference substances for fluorescence quantum yield measurements". The Journal of Physical Chemistry. 84 (14): 1871–1872. doi:10.1021/j100451a030.
  7. ^ "Detection and prevention of leaks from dams" By Antonio Plata Bedmar and Luís Araguás Araguás, Taylor & Francis, 2002, ISBN 9058093557
  8. ^ Slate, Dennis; Algeo, Timothy P.; Nelson, Kathleen M.; Chipman, Richard B.; Donovan, Dennis; Blanton, Jesse D.; Niezgoda, Michael; Rupprecht, Charles E. (2009). Bethony, Jeffrey M. (ed.). "Oral Rabies Vaccination in North America: Opportunities, Complexities, and Challenges". PLoS Neglected Tropical Diseases. 3 (12): e549. doi:10.1371/journal.pntd.0000549. PMC 2791170. PMID 20027214.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  9. ^ Naval Jelly msds with Rhodamine B
  10. ^ J.T. Baker Rhodamine B MSDS

See also