Chemodex

Acid Fuchsin

As low as CHF 103.00
In stock
Only %1 left
CDX-A0351-G02525 gCHF 103.00
CDX-A0351-G05050 gCHF 155.00
NEW
 

Specifications / Handling

More Information
Product Details
Synonyms C.I. Acid Violet 19; Fuchsin S; Fuchsin acid; Rubine S; C.I. 42685; Acid Red
Product Type Chemical
Properties
Formula C20H17N3Na2O9S3
MW 585.54
CAS 3244-88-0
RTECS DD4737000
Source/Host Chemicals Synthetic
Purity Chemicals ≥70% (Dye content)
Appearance Blue to green powder.
Solubility Soluble in DMSO (5 mg/ml) or water (1 mg/ml).
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 WZRZTHMJPHPAMU-UHFFFAOYSA-L
Smiles [Na+].[Na+].Cc1cc(cc(c1N)S([O-])(=O)=O)\C(c2ccc(N)c(c2)S([O-])(=O)=O)=C3/C=CC(=N)C(=C3)S(O)(=O)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
Product Specification Sheet
Datasheet Download PDF Download PDF

Scientific Background Information

Product Description
Acid Fuchsin is a magenta-colored acidic triphenylmethane dye widely used in histology, microbiology and staining applications. It selectively binds to cytoplasmic components and collagen-rich tissues, making it useful in differential staining protocols such as Masson’s trichrome. The dye is also applied in microbial staining techniques and as a biological stain in microscopy for enhanced contrast and visualization of cellular structures. Acid Fuchsin has also been described to be a potent Inhibitor of amyloid formation by human islet amyloid polypeptide.
Product-specific References
(1) W.L. Holman.; J. Inf. Dis. 15, 227 (1914) | (2) F.J. Leinweber & K.J. Monty; Methods Enzymol. 143, 160 (1987) | (3) L.F. Nielsen, et al.; Biotech. Histochem. 73, 71 (1998) | (4) K.A. Rider & L.M. Flick; Anal. Quant. Cytol. Histol. 26, 246 (2004) | (5) G. Vinitha & A. Ramalingam; Spectrochim. Acta A Mol. Biomol. Spectrosc. 69, 1160 (2008) | (6) F. Meng, et al.; J. Mol. Biol. 400, 555 (2010) | (7) K. Gupta, et al.; Biotech. Histochem. 87, 249 (2012) | (8) K.T. Clarke, et al.; Forensic Sci. Int. 363, 112198 (2024)
© 2017 Adipogen Life Sciences. Pictures: © 2012 Martin Oeggerli. All Rights Reserved.