Cas no 518-47-8 (Fluorescein Sodium)
Fluorescein Sodium Chemical and Physical Properties
Names and Identifiers
-
- Sodium 3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-bis(olate)
- Acid Yellow 73~C.I. 45350
- C.I. 45350
- Fluorescein Sodium Salt
- Uranine
- Fluorescein disodium salt hydrate
- C.I. Acid Yellow 73
- Acid Yellow 73 (C.I.)
- disodium 2-(3-oxo-6-oxidoxanthen-9-yl)benzoate
- Fluorescein
- Acid Yellow 73
- Uranin
- 11824 yellow
- 12417 yellow
- ful-glo
- funduscein
- furanium
- hidacid uranine
- Soap yellow
- C.I. 45350 sodium salt
- sodium fluoresceinate
- fluorescein sodium b.p
- sodium salt of hydroxy-o-carboxy-phenyl-fluorone
- resorcinol phthalein sodium
- Fluorescein, sodium derivative, sodium salt
- Soluble fluorescein
- Uranine A Extra
- Uranine K
- Uranine O
- Uranine SS
- Uranine USP XII
- Uranine WSS
- Uranine Yellow
- Yellow no. 8
- 3',6'-Dihydroxy-spiro[3H-isobenzofuran-1,9'-xanthen]-3-one disodium salt
- 3',6'-dihydroxyspiro[isobenzofuran-1(3H),9'-(9H)xanthene]-3-one, disodium salt
- 3,6-Dihydroxyxanthene-9-spiro-1'-3'H-isobenzofuran-3'-one
- 3,6-Dihydroxyxanthene-9-spiro-1'-3'H-isobenzofuran-3'-one dipotassium salt
- 3,6-Dihydroxyxanthene-9-spiro-1'-3'H-isobenzofuran-3'-one disodium salt
- 9-(o-Carboxyphenyl)-3,6-dihydroxyxanthylium dipotassium salt
- 9-(o-Carboxyphenyl)-3,6-dihydroxyxanthylium disodium salt
- 9-o-carboxyphenyl-6-hydroxy-3-isoxanthone, disodium salt
- aizen uranine
- Dihydroxyspiro[isobenzofuran-1(3H),9'-(9H)xanthen]-3-one disodium salt
- disodium 6-hydroxy-3-oxo-9-xanthene-o-benzoate
- calcocid uranine b4315
- certiqual fluoresceine
- C.I. 45350 disodium salt
- C.I. 766
- d&
- c yellow no. 8
- fluorescein, disodium salt
- fluorescein, water soluble
- fluor-i-strip a.t.
- Fluorone
- FLUORESCEIN DISODIUM SALT, TECHNICAL DYE (C.I. 45350)
- Fluorescein Sodium
- Fluorescein,disodiumsalt,pure100GR
- Fluorescein,disodiumsalt,pure500GR
- Sodium 2-(6-oxido-3-oxo-3,10-dihydroanthracen-9-yl)benzoate
- 9-(2-Carboxyphenyl)-6-hydroxy-3H-xanthen-3-one disodium salt
- Acid Yellow 73,D&C
- D and C yellow dye No 8
- Fluorescein W
- Fluorescein, disodiuM salt, pure
- fluoresceine disodium salt
- Fluorin
- YELLOW 8
- Yellow No. 8,NaFl,NaFluo
- Fluorescein 2Na
- NaFl
- NaFluo
- Sodium fluorescein
- D&C
- D&C;Yellow No. 8
- Acid Yellow 73
- Fluorescein disodium salt
- 9-(o-carboxyphenyl)-6-hydroxy-3h-xanthen-3-one,disodiumsalt
- 9’-(9h)xanthen)-3-one,3’,6’-dihydroxy-spiro(isobenzofuran-1(3hdisodiums
- 9’-[9h]xanthen]-3-one,3’,6’-dihydroxy-spiro[isobenzofuran-1(3hdisodiumsal
- 9-o-carboxyphenyl-6-hydroxy-3-isoxanthone,disodiumsalt
- abcoluraninepowders&liquids
- aizenuranine
- c.i.45350disodiumsalt
- c.i.45350sodiumsalt
- Fluorescein sodium salt,AR
-
- MDL: MFCD00167039
- Inchi: 1S/C20H12O5.Na.H/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: RXJZLVDBGRTMQG-UHFFFAOYSA-N
- SMILES: O=C1C2=CC=CC=C2C2(C3=CC=C(O)C=C3OC3=CC(O)=CC=C23)O1.[NaH]
- BRN: 3833041
Computed Properties
- Exact Mass: 376.03200
- Monoisotopic Mass: 332.068473
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 27
- Rotatable Bond Count: 0
- Complexity: 644
- Covalently-Bonded Unit Count: 3
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 76
Experimental Properties
- Color/Form: Not determined
- Density: 1.6010
- Melting Point: 320 oC
- Boiling Point: 620.8°C at 760 mmHg
- Flash Point: 232.6 oC
- PH: 8.3 (10g/l, H2O, 20℃)
- Solubility: H2O: soluble1mg/mL
- Water Partition Coefficient: 500 g/L (20 oC)
- Stability/Shelf Life: Stable.
- PSA: 81.65000
- LogP: 4.54220
- Merck: 4159
- pka: 2.2, 4.4, 6.7(at 25℃)
- Color index: 45350
- λmax: 491nm, 493.5nm, 490nm
- PH: Pink uorescence (4.0) to green uorescence (6.0)
- Sensitiveness: Sensitive to humidity
- Solubility: Soluble in water and ethanol, with strong green fluorescence and good water solubility.
- Vapor Pressure: No data available
Fluorescein Sodium Security Information
- Signal Word:Warning
- Hazard Statement: H315; H319; H335
- Warning Statement: P261; P264; P271; P280; P302+P352; P304+P340; P305+P351+P338; P312; P321; P332+P313; P337+P313; P362; P403+P233; P405; P501
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:1
- Hazard Category Code: R36
- Safety Instruction: S22-S24/25-S37/39-S26
- FLUKA BRAND F CODES:3
- RTECS:LM5425000
-
Hazardous Material Identification:
- TSCA:Yes
- Toxicity:LD50 in mice, rats (mg/kg): 4738, 6721 orally (Yankel, Loux)
- Storage Condition:Store at room temperature
- Risk Phrases:R36
- Safety Term:S26;S37/39
Fluorescein Sodium Customs Data
- HS CODE:3204200000
- Customs Data:
China Customs Code:
2932999099Overview:
2932999099. Other heterocyclic compounds containing only oxygen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Fluorescein Sodium Pricemore >>
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Fluorescein Sodium Suppliers
Fluorescein Sodium Related Literature
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
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Eunice Y.-L. Hui,Bhimsen Rout,Yaw Sing Tan,Kok-Ping Chan,Charles W. Johannes Org. Biomol. Chem., 2018,16, 389-392
Additional information on Fluorescein Sodium
Introduction to Fluorescein Sodium (CAS No: 518-47-8)
Fluorescein Sodium, with the chemical name disodium salt of 3H-benzo[de]isoquinoline-3,4-dione, is a widely recognized fluorescent dye that has found extensive applications in various scientific and medical fields. Its unique photophysical properties, including high quantum yield and strong fluorescence, make it an invaluable tool for imaging, diagnostics, and research. This compound, identified by the CAS number 518-47-8, is particularly noted for its stability and solubility in aqueous solutions, which enhances its utility in biological systems.
The chemical structure of Fluorescein Sodium consists of a benzo[de]isoquinoline core, which is a fused ring system that contributes to its remarkable fluorescence characteristics. The sodium salt form increases its solubility in water, making it highly suitable for intravenous administration and other biomedical applications. The compound's ability to emit light in the visible spectrum, particularly at a wavelength of approximately 520 nm when excited at 494 nm, makes it an ideal candidate for fluorescence microscopy and flow cytometry.
In recent years, Fluorescein Sodium has been extensively studied for its potential in bioimaging and cellular tracking. Researchers have leveraged its bright fluorescence to label various biological molecules and structures, enabling high-resolution visualization of cellular processes. For instance, studies have demonstrated its use in tracking the movement of proteins within cells, assessing the integrity of blood vessels, and monitoring neural activity. The compound's compatibility with live cells and tissues has made it a preferred choice for long-term imaging studies.
The application of Fluorescein Sodium extends beyond basic research into therapeutic applications. In clinical settings, it is commonly used as a contrast agent in ophthalmology for diagnosing retinal diseases. Its ability to highlight blood vessels and other retinal structures under fluorescence illumination has significantly improved the accuracy of diagnosing conditions such as diabetic retinopathy and macular degeneration. Additionally, Fluorescein Sodium has been employed in angiography to assess blood flow and vascular health.
Advances in nanotechnology have further expanded the utility of Fluorescein Sodium. Researchers have developed fluorescent nanoparticles conjugated with this dye for targeted drug delivery systems. These nanoparticles can be engineered to release therapeutic agents at specific sites within the body, guided by the fluorescence emitted by Fluorescein Sodium. This approach has shown promise in treating various diseases, including cancer, by enabling precise targeting and reducing side effects associated with conventional treatments.
The synthesis of Fluorescein Sodium (CAS No: 518-47-8) involves a series of organic reactions that typically begin with the condensation of resorcinol and phthalic anhydride to form fluorescein. Subsequent sodium hydrolysis converts fluorescein into its sodium salt form. The purity and quality of the final product are critical for its intended applications, particularly in biomedical research where impurities can interfere with experimental results. High-purity grades of Fluorescein Sodium are available from reputable chemical suppliers to ensure reliable performance.
The environmental impact of using Fluorescein Sodium has also been a subject of interest. While it is generally considered safe for biological applications when used appropriately, researchers are exploring methods to minimize its environmental footprint. For example, efforts are being made to develop biodegradable formulations that can break down into non-toxic products after their use. Such innovations aim to reduce waste while maintaining the efficacy of this valuable fluorescent dye.
In conclusion, Fluorescein Sodium, identified by CAS No 518-47-8, is a versatile fluorescent dye with significant contributions across multiple scientific disciplines. Its unique properties make it indispensable for bioimaging, diagnostics, and therapeutic applications. As research continues to uncover new uses for this compound, its importance in advancing medical science is likely to grow even further. The ongoing development of innovative formulations and applications ensures that Fluorescein Sodium will remain at the forefront of scientific discovery for years to come.