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F8129

Sigma-Aldrich

Acid Fuchsin

Powder

Synonyme(s) :

Acid Violet 19, Fuchsin S, Fuchsin acid, Rubine S

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About This Item

Formule empirique (notation de Hill):
C20H17N3Na2O9S3
Numéro CAS:
Poids moléculaire :
585.54
Numéro C.I. (Colour Index):
42685
Numéro Beilstein :
4111656
Numéro CE :
Code UNSPSC :
12171500
ID de substance PubChem :
Nomenclature NACRES :
NA.47

product name

Acid Fuchsin, used in tissue staining

Niveau de qualité

Forme

powder

Composition

Dye content, ~70%

Couleur

blue-green

Solubilité

H2O: 1 mg/mL

Application(s)

diagnostic assay manufacturing
hematology
histology

Température de stockage

room temp

Chaîne 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

InChI

1S/C20H19N3O9S3.2Na/c1-10-6-13(9-18(20(10)23)35(30,31)32)19(11-2-4-14(21)16(7-11)33(24,25)26)12-3-5-15(22)17(8-12)34(27,28)29;;/h2-9,23H,21-22H2,1H3,(H,24,25,26)(H,27,28,29)(H,30,31,32);;/q;2*+1/p-2

Clé InChI

WZRZTHMJPHPAMU-UHFFFAOYSA-L

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Description générale

Acid Fuchsin is mainly used as a diachrome and is part of the connective tissue stains. It also works as a pH indicator.

Application

Acid Fuchsin has been used in tissue sections for Masson′s trichrome staining. It has been used as a marker to trace ingestion of solutions by green peach aphids.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Roberto Luongo et al.
The International journal of periodontics & restorative dentistry, 28(6), 551-557 (2009-01-17)
Platform switching is a concept recently introduced in implant dentistry. It is intended to reduce the crestal bone loss that is commonly found around implants exposed to the oral environment. The aim of this study was to examine biopsy specimens
Fanling Meng et al.
Journal of molecular biology, 400(3), 555-566 (2010-05-11)
Islet amyloid polypeptide (IAPP), also known as amylin, is responsible for amyloid formation in type 2 diabetes. The formation of islet amyloid is believed to contribute to the pathology of the disease by killing beta-cells, and it may also contribute
Jong-Hwan Lee et al.
Neuroscience letters, 325(2), 129-133 (2002-06-05)
Ginsenosides are known to attenuate glutamate-induced cell injuries in vitro. We investigated the in vivo effect of ginsenosides on kainic acid (KA)-induced neurotoxicity in rat hippocampus using the methods of acid fuchsin (AF) staining and heat-shock protein-70 (HSP-70) immunoreactivity to
Shili Xiao et al.
ACS applied materials & interfaces, 1(12), 2848-2855 (2010-04-02)
We report a facile approach to synthesizing and immobilizing zero-valent iron nanoparticles (ZVI NPs) onto polyelectrolyte (PE) multilayer-assembled electrospun polymer nanofibers for potential environmental applications. In this approach, negatively charged cellulose acetate (CA) nanofibers fabricated by electrospinning were assembled with
Hongtao Huang et al.
Nanotechnology, 23(10), 105502-105502 (2012-03-01)
Zn-doped SnO(2) nanorods have been prepared by a simple hydrothermal method on a large scale. The as-prepared samples were characterized by x-ray powder diffraction, scanning electron microscope, transmission electron microscope, energy dispersive spectrometer, x-ray photoelectron spectroscopy, UV-vis absorption spectra and

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