Sulforhodamine B (Highly Pure)


Catalog Number: B2012336 (5 mg)
Sulforhodamine B (Highly Pure) is a high quality Sulforhodamine B sodium salt used as an an aminoxanthene dye. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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Sulforhodamine B (Highly Pure)
Catalog number: B2012336
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 5 mg
Molecular Weight or Concentration: 580.7 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: 3,6-bis(diethylamino)-9-(2,4-disulfophenyl)-xanthylium
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Vichai V, Kirtikara K. Sulforhodamine B colorimetric assay for cytotoxicity screening Nat Protoc. 2006;1(3):1112-6.
2: Nguyen TL, Perlman CE. Sulforhodamine B and exogenous surfactant effects on alveolar surface tension under acute respiratory distress syndrome conditions J Appl Physiol (1985). 2020 Dec 1;129(6):1505-1513.
3: Wu Y, Nguyen TL, Perlman CE. Intravenous sulforhodamine B reduces alveolar surface tension, improves oxygenation, and reduces ventilation injury in a respiratory distress model J Appl Physiol (1985). 2021 May 1;130(5):1305-1316.
4: Rodrigues ET, Pardal MA, Pereira E, Monteiro JF, Certal AC, Oliveira PJ. H9c2(2-1)-based sulforhodamine B assay as a possible alternative in vitro platform to investigate effluent and metals toxicity on fish Chemosphere. 2021 Jul;275:130009.
5: Piccolo KA, McNeil B, Crouse J, Lim SJ, Bickers SC, Hopkins WS, Dieckmann T. Ligand specificity and affinity in the sulforhodamine B binding RNA aptamer Biochem Biophys Res Commun. 2020 Aug 27;529(3):666-671.
6: van Tonder A, Joubert AM, Cromarty AD. Limitations of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay when compared to three commonly used cell enumeration assays BMC Res Notes. 2015 Feb 20;8:47.
7: Voigt W. Sulforhodamine_B assay and chemosensitivity Methods Mol Med. 2005;110:39-48.
8: Chodosh J, Dix RD, Howell RC, Stroop WG, Tseng SC. Staining characteristics and antiviral activity of sulforhodamine_B and lissamine green B Methods Mol Med. 2005;110:39-48. doi: 10.1385/1-59259-869-2:039.
9: Turner PR, Yoshida M, Ali MA, Cabral JD. Melt Electrowritten Sandwich Scaffold Technique Using Sulforhodamine_B to Monitor Stem Cell Behavior Tissue Eng Part C Methods. 2020 Oct;26(10):519-527.
10: Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR. New colorimetric cytotoxicity assay for anticancer-drug screening J Natl Cancer Inst. 1990 Jul 4;82(13):1107-12.

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