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    Basic Fuchsin

    Available from stock

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      Basic Fuchsin

      SKU
      F0102

      Category: Fluorescent Detection

      Synonyms
      C.I. Basic Violet 14, Fuchsine Basic, Basic Magenta, Rosaniline, C.I. 42510, Aizen Magenta
      632-99-5
      CAS-Number
      C20H20ClN3
      Molecular Formula
      337.85
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥80.0% (dye content)
      Appearance
      Green powder
      UV/Vis
      545 - 555 nm

      Properties

      Solvents
      Soluble in water, methanol or DMSO.
      Melting Point
      205° C
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Hazard statements
      H351
      Precautionary statements
      P201 - P308 + P313
      GHS Symbol
      GHS08
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      Basic Fuchsin is a triphenylmethane dye renowned for its intense magenta color. It is primarily used in microbiological and histological staining as it has a strong affinity for nucleic acids and cellular components, making it invaluable in the visualization of cell structures under a microscope. The mechanism of action of Basic Fuchsin involves its basic properties, which allow it to bind to acidic components of cells, particularly nucleic acids, through electrostatic interactions. In research, Basic Fuchsin is extensively used in the Gram staining procedure, a fundamental technique for bacterial classification and identification. In this process, it serves as a primary stain that colors all cells. However, its retention in Gram-positive bacteria, due to their thicker peptidoglycan layer, contrasts sharply with its removal from Gram-negative bacteria during a decolorization step, demonstrating its selective staining capabilities. Additionally, Basic Fuchsin is used in other histological stains, such as the Schiff reagent for the periodic acid-Schiff reaction, which is essential for identifying polysaccharides such as glycogen in tissues and is also used for staining of acid-fast bacteria (AFB). Through these applications, Basic Fuchsin continues to be a pivotal tool in both clinical diagnostics and biological research, providing critical insights into microbial morphology and cellular biochemistry.
      Smiles
      NC1=C(C)C=C(/C(C2=CC=C(N)C=C2)=C3C=CC(C=C/3)=N)C=C1.Cl
      InChi Key
      NIKFYOSELWJIOF-SVFFXJIWSA-N
      References
      (1) E. Adams; Stain Technol. 50, 227 (1975) , (2) D.K. Cooper; Histochem. J. 9, 285 (1977) , (3) K. Pihlman & E. Linder; Histochem. 79, 157 (1983) , (4) T.J. Beveridge; Biotech. Histochem. 76, 111 (2001) , (5) T. Frisch, et al.; Eur. Arch. Otorhinolaryngol. 258, 55 (2001) , (6) R. Coico, et al.; Curr. Protoc. Microbiol. Appendix 3-3C (2005) , (7) C. Gordon, et al.; Int. J. Tuberc. Lung. Dis. 13, 130 (2009) , (8) M. Chen, et al.; Bioanalysis 5, 1545 (2013) , (9) B. Pathrose, et al.; Spectrochim. Acta A Mol. Biomol. Spectrosc. 128, 522 (2014) , (10) B. Pathrose, et al.; J. Fluoresc. 24, 895 (2014)
      InChi
      InChI=1S/C20H19N3.ClH/c1-13-12-16(6-11-19(13)23)20(14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15;/h2-12,21H,22-23H2,1H3;1H

      Basic Fuchsin is a triphenylmethane dye renowned for its intense magenta color. It is primarily used in microbiological and histological staining as it has a strong affinity for nucleic acids and cellular components, making it invaluable in the visualization of cell structures under a microscope. The mechanism of action of Basic Fuchsin involves its basic properties, which allow it to bind to acidic components of cells, particularly nucleic acids, through electrostatic interactions. In research, Basic Fuchsin is extensively used in the Gram staining procedure, a fundamental technique for bacterial classification and identification. In this process, it serves as a primary stain that colors all cells. However, its retention in Gram-positive bacteria, due to their thicker peptidoglycan layer, contrasts sharply with its removal from Gram-negative bacteria during a decolorization step, demonstrating its selective staining capabilities. Additionally, Basic Fuchsin is used in other histological stains, such as the Schiff reagent for the periodic acid-Schiff reaction, which is essential for identifying polysaccharides such as glycogen in tissues and is also used for staining of acid-fast bacteria (AFB). Through these applications, Basic Fuchsin continues to be a pivotal tool in both clinical diagnostics and biological research, providing critical insights into microbial morphology and cellular biochemistry.

      SKU: F0102 Category: Fluorescent Detection
      • Additional information

      Additional information

      Synonyms

      C.I. Basic Violet 14, Fuchsine Basic, Basic Magenta, Rosaniline, C.I. 42510, Aizen Magenta

      Purity

      ≥80.0% (dye content)

      Appearance

      Green powder

      CAS-Number

      632-99-5

      Molecular Formula

      C20H20ClN3

      Molecular Weight

      337.85

      Solvents

      Soluble in water, methanol or DMSO.

      Melting Point

      205° C

      Smiles

      NC1=C(C)C=C(/C(C2=CC=C(N)C=C2)=C3C=CC(C=C/3)=N)C=C1.Cl

      InChi Key

      NIKFYOSELWJIOF-SVFFXJIWSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Hazard statements

      H351

      Precautionary statements

      P201 – P308 + P313

      GHS Symbol

      GHS08

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) E. Adams; Stain Technol. 50, 227 (1975), (2) D.K. Cooper; Histochem. J. 9, 285 (1977), (3) K. Pihlman & E. Linder; Histochem. 79, 157 (1983), (4) T.J. Beveridge; Biotech. Histochem. 76, 111 (2001), (5) T. Frisch, et al.; Eur. Arch. Otorhinolaryngol. 258, 55 (2001), (6) R. Coico, et al.; Curr. Protoc. Microbiol. Appendix 3-3C (2005), (7) C. Gordon, et al.; Int. J. Tuberc. Lung. Dis. 13, 130 (2009), (8) M. Chen, et al.; Bioanalysis 5, 1545 (2013), (9) B. Pathrose, et al.; Spectrochim. Acta A Mol. Biomol. Spectrosc. 128, 522 (2014), (10) B. Pathrose, et al.; J. Fluoresc. 24, 895 (2014)

      InChi

      InChI=1S/C20H19N3.ClH/c1-13-12-16(6-11-19(13)23)20(14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15;/h2-12,21H,22-23H2,1H3;1H

      Quantity

      25 g, 100 g, Bulk

      cdx-UV/Vis

      545 – 555 nm

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