Chemodex

Alizarin Red S

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Product Details
Synonyms 3,4-Dihydroxy-9,10-dioxo-2-anthracenesulfonic acid sodium salt; C.I. 58005; Alizarin Carmine; Alizarin Red; Alizarinsulfonate; Ahcoquinone Red S; Alizarin sulfonate sodium; Chrome Red Alizarine
Product Type Chemical
Properties
Formula C14H7NaO7S
MW 342.26
CAS 130-22-3
RTECS CB1095300
Source/Host Chemicals Synthetic
Purity Chemicals ≥70% (Dye content)
Appearance Brownish yellow powder.
Solubility Soluble in DMSO (10mg/ml) or water (1mg/ml).
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key HFVAFDPGUJEFBQ-UHFFFAOYSA-M
Smiles [Na+].Oc1c(O)c(cc2C(=O)c3ccccc3C(=O)c12)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
Description
Alizarin Red S is a well-established anionic anthraquinone dye widely used as a pH indicator or for the detection and quantification of calcium and other divalent metal ions. It forms a bright red to orange-red complex with calcium salts, making it a standard reagent for histological staining and cell culture assays involving mineralization. In biomedical research, Alizarin Red S is most commonly used to assess osteogenic differentiation by staining calcium deposits in cultured cells and tissue sections. The dye is also employed in analytical chemistry and materials science for metal ion binding studies due to its strong chelation properties. Its strong color response and reliable metal-binding properties make it an excellent choice for osteogenesis studies, histological staining, and spectrophotometric analysis in both research and quality control laboratories. It acts as a colorometric pH indicator. 1st transition range: pH 4.3 - pH 6.3 Lightly yellow - pink/red. 2nd transition range: pH 9.4 - pH 12.0 Brown orange - violet.
Product References
[1] K.F. Adkins; Stain Technol. 40, 69 (1965) | [2] H. Puchtler, et al.; J. Histochem. Cytochem. 17, 110 (1969) | [3] P. Virtanen & K. Isotupa; Acta Anat. 108, 202 (1980) | [4] F. Eggelmeijer, et al.; Clin. Exp. Rheumatol. 9, 11 (1991) | [5] K. Basavaiah, et al.; Talanta 50, 887 (1999) | [6] G. Springsteen & B. Wang; Chem. Commun. 7, 1608 (2001) | [7] I. Sahin & N. Nakiboglu; Anal. Chim. Acta 572, 253 (2006) | [8] S.A. Sangsefedi, et al.; J. Fluoresc. 28, 815 (2018) | [9] W. Ma, et al.; Polymers 11, 165 (2019) | [10] A. Bernar, et al.; Int. J. Mol. Sci. 24, 723 (2022) | [11] C.A.N. Catalan, et al.; Molecules 30, 3286 (2025)
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