Chemodex

Fluorescein dipropionate

CHF 272.00
In stock
CDX-F0088-G0011 gCHF 272.00
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Product Details
Synonyms FDPr; 3',6'-Bis(1-oxopropoxy)spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one
Product Type Chemical
Properties
Formula

C26H20O7

MW 444.43
CAS 7276-28-0
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (NMR)
Appearance Off-white powder.
Solubility Soluble in ethanol or chloroform.
Identity Determined by 1H-NMR.
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 NXIABCNYUKDBQI-UHFFFAOYSA-N
Smiles O=C(O1)C2=C(C=CC=C2)C31C4=CC=C(OC(CC)=O)C=C4OC5=C3C=CC(OC(CC)=O)=C5
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Fluorescein is the most important xanthene dye widely used for labeling and sensing biomolecules. It has a high extinction coefficient and fluorescence quantum yield in aqueous solution, and its excitation wavelength is in the visible range. However, fluorescein also has some obvious deficiencies. Particularly its hydrophilic nature limits its application to the detection of enzymes, therefore fluorescein esters are a useful alternative. Fluorescein esters, such as fluorescein dipropionate, are nonfluorescent, but they can be cleaved by intracellular enzymes to yield fluorescent products, such as fluorescein. The rate of change in the fluorescence of the solution, due to the production of fluorescein, is measured and correlated with enzyme activity. Therefore, fluorescein esters could be used as fluorometric determination probes of enzymes. Fluorescein dipropionate could also be used as a building block or intermediate in synthesis of fluorescent probes.

Product References

(1) B. Rotman & B.W. Papermaster; PNAS 55, 134 (1966) | (2) F.-Y. Ge, et al.; Dyes Pigments 72, 322 (2007) | (3) M. Poznik & B. Koenig; Org. Biomol. Chem. 12, 3175 (2014)

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