Chemodex

Phenol red

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Product Details
Synonyms Phenolsulfonphthalein; Sulfonphthal; PSP; NSC 10459; 3,3-Bis(p-hydroxyphenyl)-2,1-3H-benzoxathiole 1,1-dioxide
Product Type Chemical
Properties
Formula C19H14O5S
MW 354.38
CAS 143-74-8
RTECS SJ7490000
Source/Host Chemicals Synthetic
Purity Chemicals ≥95% (Dye content)
Appearance Powder.
Solubility Soluble in DMSO. Slightly soluble in water, ethanol or methanol.
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 BELBBZDIHDAJOR-UHFFFAOYSA-N
Smiles O=S1(C2=CC=CC=C2C(C3=CC=C(O)C=C3)(C4=CC=C(O)C=C4)O1)=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
Phenol red belongs to the class of triphenylmethane dyes and is a widely used pH indicator and biological reagent, valued for its clear colorimetric response over a pH range of 6.8 to 8.4, transitioning from yellow to red. It is commonly employed in cell culture media to monitor pH changes during cell growth and metabolism, ensuring optimal conditions for biological assays. Widely used in culture media, phenol red identifies pH changes from neutral (red) to acidic (yellow) values. Typically a change in color from red to yellow indicates high rates of cellular death when used in tissue cultures. Beyond its role as a pH indicator, phenol red serves in analytical chemistry for titrations, as a visual marker in enzyme activity assays, and in the development of colorimetric sensors. In different protocols, it is used to detect hydrogen peroxide. Visual transition intervals: 1.2-3.0, brown-orange to yellow (1st transition range); 6.5-8.0, brownish-yellow to red-violet (2nd transition range).
Product References
(1) Y. Berthois, et al.; PNAS 83, 2496 (1986) | (2) K. Higaki, et al.; Pharm. Res. 5, 309 (1988) | (3) P. Yuan & D.R. Walt; J. Fluoresc. 2, 231 (1992) | (4) W. Yao & R.H. Byrne; Environ. Sci. Technol. 35, 1197 (2001) | (5) A. Sundarakrishnan, et al.; Acta Biomater. 42, 102 (2016) | (6) A. Morgan, et al.; Chem. Biol. Interact. 310, 108739 (2019) | (7) C. Sun, et al.; Spectrochim. Acta A Mol. Biomol. Spectrosc. 296, 122663 (2023) | (8) R.E. Foreman, et al.; Bioanalysis 16, 575 (2024) | (9) M. Vera, et al.; Free Radic. Biol. Med. 222, 397 (2024)
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