Date published: 2025-11-4

1-800-457-3801

SCBT Portrait Logo
Seach Input

New Fuchsin (CAS 3248-91-7)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Basic Violet 2; Fuchsin N, Magenta™ III
CAS Number:
3248-91-7
Molecular Weight:
365.91
Molecular Formula:
C22H24ClN3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

New Fuchsin is an organic dye extensively employed in scientific research, specifically in biochemistry. As a member of the triphenylmethane group of dyes, it exhibits a strong attraction towards proteins, rendering it invaluable for examining protein structure and function. Although the precise mechanism of action remains partially elusive, it is presumed to be linked to its affinity for proteins. By binding to proteins, New Fuchsin enables easy staining and visualization. Furthermore, the dye displays interaction capabilities with various molecules, including DNA, enabling its utilization in the detection of their presence within a sample.


New Fuchsin (CAS 3248-91-7) References

  1. In situ hybridization for the detection of chicken anaemia virus in experimentally-induced infection and field outbreaks.  |  Nielsen, OL., et al. 1995. Avian Pathol. 24: 149-55. PMID: 18645772
  2. Western blot analysis for 4-hydroxy-2-nonenal (HNE)-modified proteins in paraquat-treated mice.  |  Kurisaki, E. and Hiraiwa, K. 2009. Leg Med (Tokyo). 11 Suppl 1: S431-3. PMID: 19261533
  3. Mineral trioxide aggregate for direct pulp capping: a histologic comparison with calcium hydroxide in rat molars.  |  Dammaschke, T., et al. 2010. Quintessence Int. 41: e20-30. PMID: 20165737
  4. Ovariectomized mouse uterotrophic assay of 36 chemicals.  |  Ohta, R., et al. 2012. J Toxicol Sci. 37: 879-89. PMID: 23037998
  5. Physicochemical properties and photodynamic activity of novel derivatives of triarylmethane and thiazine.  |  Montes de Oca, MN., et al. 2013. Arch Pharm (Weinheim). 346: 255-65. PMID: 23494746
  6. Standardization of the Feulgen-Schiff technique. Staining characteristics of pure fuchsin dyes; a cytophotometric investigation.  |  Schulte, E. and Wittekind, D. 1989. Histochemistry. 91: 321-31. PMID: 2732097
  7. Identification of synthetic dyes magenta III (new fuchsin) and rhodamine B as common adulterants in commercial saffron.  |  Bhooma, V., et al. 2020. Food Chem. 309: 125793. PMID: 31699557
  8. Hydrophilic dyes as photosensitizers for photopolymerization of dental adhesives.  |  Abedin, F., et al. 2020. J Dent. 99: 103405. PMID: 32522687
  9. Separation of fuchsin homologs using high performance liquid chromatography.  |  Sehlinger, TE. and Nettleton, GS. 1987. Stain Technol. 62: 291-7. PMID: 3424392
  10. The alkaline phosphatase anti-alkaline phosphatase technique in dermatopathology.  |  Schaumburg-Lever, G. 1987. J Cutan Pathol. 14: 6-9. PMID: 3549814
  11. Separation of fuchsin analogs using thin layer chromatography.  |  Nettleton, GS. and Martin, AW. 1979. Stain Technol. 54: 213-6. PMID: 516091
  12. Staining mycobacteria with carbolfuchsin: properties of solutions prepared with different samples of basic fuchsin.  |  Harada, K., et al. 1976. Microsc Acta. 78: 21-7. PMID: 58364
  13. Histologic study of the attachment of muscles to the rat mandible.  |  Chong, DA. and Evans, CA. 1982. Arch Oral Biol. 27: 519-27. PMID: 6957168
  14. Improved double immunohistochemical staining method for cryostat and paraffin wax sections, combining alkaline phosphatase anti-alkaline phosphatase and indirect immunofluorescence.  |  Tao, Q., et al. 1994. J Clin Pathol. 47: 597-600. PMID: 8089213

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

New Fuchsin, 25 g

sc-487586
25 g
$82.00