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Key Documents

568856

Sigma-Aldrich

Fluorescein o-acrylate

95%

Sinonimo/i:

3’-Acryloxyspirobenzo[c]-furan[1,9’]xanthen-3-one, Acryloyloxy fluorescein

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About This Item

Formula empirica (notazione di Hill):
C23H14O6
Numero CAS:
Peso molecolare:
386.35
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.23

Saggio

95%

Forma fisica

solid

Punto di fusione

231-233 °C (lit.)

λmax

490 nm

Temperatura di conservazione

2-8°C

Stringa SMILE

Oc1ccc2c(Oc3cc(OC(=O)C=C)ccc3C24OC(=O)c5ccccc45)c1

InChI

1S/C23H14O6/c1-2-21(25)27-14-8-10-18-20(12-14)28-19-11-13(24)7-9-17(19)23(18)16-6-4-3-5-15(16)22(26)29-23/h2-12,24H,1H2
VYLDMXSRCVCHNE-UHFFFAOYSA-N

Descrizione generale

Fluorescein o-acrylate is a fluorescent monomer with high quantum efficiency in aqueous media. Its excitation and emission wavelength are in the range of visible light. It can be copolymerized with a variety of monomers such as acrylic acid, styrene and acrylamide which facilitate the attachment of fluorescein with macromolecules.

Applicazioni

Fluorescein o-acrylate can be used in the formation of fluorescent probes for application in bio-imaging. It can also be used in the synthesis of molecularly imprinted polymers (MIPs). It also facilitates the demarcation of different layers in fluorescence microscopy.
Fluorescent monomer

Pittogrammi

Exclamation markEnvironment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Fluorescent molecularly imprinted polymer film binds glucose with a concomitant changes in fluorescence
Manju S, et al.
Biosensors And Bioelectronics, 26(2), 894-897 (2010)
Feifei Wang et al.
Polymers, 11(12) (2019-11-30)
In this study, we established a new fluorescent indicator platform. The responsive element consists of poly(N-isopropylacrylamide) nanospheres that include small percentages of fluorescein and a ligand, anilinodiacetate (phenylIDA). Nanosphere diameters were determined to be in the range from 50 to
Benxin Jing et al.
Soft matter, 13(28), 4881-4889 (2017-06-21)
Coacervate complexes that are liquid-liquid separated complex materials are often formed by stoichiometrically mixing oppositely charged polyelectrolytes in salted aqueous solution. Entropy-driven ion pairing, resulting from the release of counterions near polyelectrolytes, has been identified as the primary driving force
Synthesis and photophysical behavior of a water-soluble fluorescein-bearing polymer for Fe 3+ ion sensing
Wang B, et al.
Journal of Polymer Research, 15(6), 427-433 (2008)
Sequential formation of covalently bonded hydrogel multilayers through surface initiated photopolymerization
K?z?lel S, et al.
Biomaterials, 27(8), 1209-1215 (2006)

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