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About This Item
Empirical Formula (Hill Notation):
C20H12O5
CAS Number:
Molecular Weight:
332.31
UNSPSC Code:
12171500
Colour Index Number:
45350:1
NACRES:
NA.47
PubChem Substance ID:
EC Number:
219-031-8
MDL number:
Beilstein/REAXYS Number:
94324
Product Name
Fluorescein (free acid), Dye content 95 %
form
powder
Quality Segment
composition
Dye content, 95%
technique(s)
titration: suitable
color
orange to red-brown
mp
320 °C (lit.)
λmax
496 nm
ε (extinction coefficient)
≥12000 at 282-286 nm, ≥39000 at 236-240 nm, ≥70000 at 488-492 nm
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
Oc1ccc2c(Oc3cc(O)ccc3C24OC(=O)c5ccccc45)c1
InChI
1S/C20H12O5/c21-11-5-7-15-17(9-11)24-18-10-12(22)6-8-16(18)20(15)14-4-2-1-3-13(14)19(23)25-20/h1-10,21-22H
InChI key
GNBHRKFJIUUOQI-UHFFFAOYSA-N
General description
Application
Fluorescein (free acid) is widely used as a fluorescent stain and trace for many living cells and tissue applications. It is also suitable as a marker for the study of motility of bile canaliculi. Some of the clinical applications are evaluating the ocular surface and delineation of brain regions lacking a blood-brain barrier to permit accurate surgical resection of malignant glioma. Fluorescein angiography helps investigate changes in retinal blood supply. Fluorescein also plays a role as a physiological tracer to characterize the salmon′s intestinal permeability (Schep et al., 1998), and for the fluorophotometric measurement of aqueous humor flow. It is widely employed as a quantum yield standard.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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