Rhodamine B: Difference between revisions

From CAMEO
Jump to navigation Jump to search
No edit summary
 
(4 intermediate revisions by the same user not shown)
Line 5: Line 5:


[[File:Rhodamine B_abs.ems.jpg|thumb|Absorption and fluorescence emission spectra]]
[[File:Rhodamine B_abs.ems.jpg|thumb|Absorption and fluorescence emission spectra]]
[[[SliderGallery rightalign|PV001 sun rhodamine b 221-0035.TIF~FTIR 221-0035(MFA)|PV1 rhodamine b (magruder mm0107-dc).TIF~FTIR mm0107-dc(MFA)|Pv1 rhodamine B (magruder mm0122-dc).TIF~FTIR mm0122-dc(MFA)|Pv1 rhodamine B (magruder mm1219-dc).TIF~FTIR mm1219-dc(MFA)|Rhodamine (Forbes MFA 44) copy.tif~Raman (MFA)|f44sem.jpg~SEM|f44edsbw.jpg~EDS|rhodamine b.jpg~Chemical structure]]]
== Synonyms and Related Terms ==
== Synonyms and Related Terms ==


Line 11: Line 10:


== Comparisons ==
== Comparisons ==
Rhodamine B variations with some properties and descriptions
{| class="wikitable"  
{| class="wikitable"  
|-
|-
! Name
! CI Number
! Formula
! Other names
! Other names
! Laked form
! Laked form
! Comments
! Comments
|-
|-
| [[Rhodamine B]]
| Rhodamine 610; Basic Violet 10
| 45170
| C28H31CIN2O3
| Rhodamine 610
|
| rowspan="2" | fluorescence microscopy and laser dyes, pH  indicators; water tracer
|-
|
|
|
| Basic Violet 10
|  
|  
| identification by fluorescence microscopy and laser dyes; used as pH  indicator and water tracer
|-
|-
|
|
|
| D&C Red #19
| D&C Red #19
|  
|  
| formerly used in drugs and  cosmetics but was removed from list in 1984 as a suspected carcinogen
| formerly used in drugs and  cosmetics but was removed from list in 1984 as a suspected carcinogen
|-
|-  
|
|
|
| Solvent red 49
| Solvent red 49
|  
|  
| fluorescent red dye used in wood stains and  coating, printing inks and leather finishes.
| fluorescent red dye used in wood stains and  coating, printing inks and leather finishes.
|-
|-
|
|
|
| Pigment Violet 1
| Pigment Violet 1
| phosphotungstomolybdic  acid salt
| phosphotungstomolybdic  acid salt
| bright reddish-violet with high color strength and good lightfastness; used in printing inks, textile  printing, and, in some cases, plastics due to its high gloss and vivid shade
| introduced in 1924; bright reddish-violet with high color strength and good lightfastness; used in printing inks, textile  printing, and, in some cases, plastics due to its high gloss and vivid shade
|-
|-  
|
| Pigment  Red 173; Rhodamine Red; Cosmetic Rubine
|
|
| Pigment  Red 173
| aluminum  salt
| aluminum  salt
| brilliant pink to magenta used in  inks, powder coatings, industrial  paints, colored glass and plastic  industries; Extensively used in cosmetic  products; also called Rhodamine red and Cosmetic Rubine
| brilliant pink to magenta used in  inks, powder coatings, industrial  paints, colored glass and plastics; Extensively used in cosmetic  products
|}
|}
<!--{| class="wikitable"
<!--{| class="wikitable"
Line 73: Line 49:
|-
|-
|}-->
|}-->
[[[SliderGallery rightalign|PV001 sun rhodamine b 221-0035.TIF~FTIR 221-0035(MFA)|PV1 rhodamine b (magruder mm0107-dc).TIF~FTIR mm0107-dc(MFA)|Pv1 rhodamine B (magruder mm0122-dc).TIF~FTIR mm0122-dc(MFA)|Pv1 rhodamine B (magruder mm1219-dc).TIF~FTIR mm1219-dc(MFA)|Rhodamine (Forbes MFA 44) copy.tif~Raman (MFA)|f44sem.jpg~SEM|f44edsbw.jpg~EDS|rhodamine b.jpg~Chemical structure]]]


== Risks ==
== Risks ==

Latest revision as of 14:56, 18 April 2026

Rhodamine

Description

rhodamine at 100x

A strong, bright red fluorescent dye. Rhodamine B is a basic dye that was developed in 1887 by Ceresole. It is used as textile and paper dye, as a pigment, and as a staining reagent for the detection of fats and oils. Some oil modified materials such as alkyds and urethanes will also stain with rhodamine (Wolbers et al 1990). Rhodamine B has been used as a fluorescent colorant in inks (ballpoint, printing), wood stains, distemper paints, colored glass, plastics, and shoe polish.

Absorption and fluorescence emission spectra

Synonyms and Related Terms

Basic Violet 10; CI 45170; tetraethylrhodamine; D&C Red No. 19, Solvent Red 49; Pigment Violet 1 (phosphotungstomolybdic acid salt); Pigment Red 173 (aluminum salt); Rhodamine (Deut.); Rodamina B (Esp.); rodamina B (Port.); rhodamine B (Fr.)

Comparisons

Rhodamine B variations with some properties and descriptions

Other names Laked form Comments
Rhodamine 610; Basic Violet 10 identification by fluorescence microscopy and laser dyes; used as pH indicator and water tracer
D&C Red #19 formerly used in drugs and cosmetics but was removed from list in 1984 as a suspected carcinogen
Solvent red 49 fluorescent red dye used in wood stains and coating, printing inks and leather finishes.
Pigment Violet 1 phosphotungstomolybdic acid salt introduced in 1924; bright reddish-violet with high color strength and good lightfastness; used in printing inks, textile printing, and, in some cases, plastics due to its high gloss and vivid shade
Pigment Red 173; Rhodamine Red; Cosmetic Rubine aluminum salt brilliant pink to magenta used in inks, powder coatings, industrial paints, colored glass and plastics; Extensively used in cosmetic products

FTIR 221-0035(MFA)

PV001 sun rhodamine b 221-0035.TIF

FTIR mm0107-dc(MFA)

PV1 rhodamine b (magruder mm0107-dc).TIF

FTIR mm0122-dc(MFA)

Pv1 rhodamine B (magruder mm0122-dc).TIF

FTIR mm1219-dc(MFA)

Pv1 rhodamine B (magruder mm1219-dc).TIF

Raman (MFA)

Rhodamine (Forbes MFA 44) copy.tif

SEM

F44sem.jpg

EDS

F44edsbw.jpg

Chemical structure

Rhodamine b.jpg


Risks

  • Listed as carcinogen and mutagen.
  • Harmful if swallowed
  • Can cause eye damage and allergic reactions in skin
  • Store in glass containers as it is absorbed by plastics
  • ThermoFisher: SDS

Physical and Chemical Properties

  • Soluble in water, alcohols, and polar solvents.
  • Decomposes in chlorinated solutions.
  • Maximum absorption wavelength = 545 nm.
  • Maximum emission wavelength = 625 nm.
  • Composition = C28H31ClN2O3 (mol. wt. = 478.68 g/mol)
  • CAS = 81-88-9
  • Melting Point = 210-211 C

Resources and Citations

  • A. Schaening, M. Schreiner, D. Jembrih-Simbuerger, 'Identification and Classification of Synthetic Organic Pigments of a Collection of the 19th and 20th century by FTIR' The Sixth Infrared and Raman Users Group Conference (IRUG6), Florence Italy, 2004.
  • R. Wolbers, N. Sterman and C. Stavroudis, "Notes for Workshop on New Methods in the Cleaning of Paintings", 1990, GCI, Los Angeles.
  • Website for absorption/fluorescent spectra: http://www.omlc.ogi.edu/spectra/PhotochemCAD/html/rhodamineB.html
  • Reed Kay, The Painter's Guide To Studio Methods and Materials, Prentice-Hall, Inc., Englewood Cliffs, NJ, 1983
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Monona Rossol, The Artist's Complete Health and Safety Guide, Allworth Press, New York, 1994
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 8349
  • Dye History: www.straw.com/sig/dyehist - discovered 1887
  • Aldrich Chemical Catalog Comment: p. 1299
  • Colour Index International online at www.colour-index.org
  • CHSOS: Spectra (XRF, Raman, Reflectance) on PR 173
  • Wikipedia: Rhodamine B Accessed Dec. 2025