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5 (6) -Carboxy-eosin

CAT: 0804-HY-D0051Size: 1 EachDry Ice: NoHazardous: No
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Description
5 (6) -Carboxy-eosin is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells.
CAS Number
132201-84-4
UNSPSC
12171500
Hazard Statement
H315-H319-H335
Target
Fluorescent Dye
Type
Dye Reagents
Related Pathways
Others
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/5-6-carboxy-eosin.html
Solubility
10 mM in DMSO
Smiles
BrC1=CC2=C(C3=CC(Br)=C(C(Br)=C3OC2=C(C1=O)Br)O)C4=C(C=C(C=C4)C(O)=O)C(O)=O.BrC5=CC6=C(C7=CC(Br)=C(C(Br)=C7OC6=C(C5=O)Br)O)C8=C(C=CC(C(O)=O)=C8)C(O)=O
Molecular Formula
C21H8Br4O7
Molecular Weight
691.90
Precautions
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P362+P364-P403+P233-P405-P501
References & Citations
[1]Sultana M, et al. A review on experimental chemically modified activated carbon to enhance dye and heavy metals adsorption[J]. Cleaner engineering and technology, 2022, 6: 100382.
Shipping Conditions
Room temperature
Scientific Category
Dye Reagents
Clinical Information
No Development Reported

Chemical Information

5(6)-Carboxyeosin
CAS Number132201-84-4
PubChem CID44119976
IUPAC Name2-(2,4,5,7-tetrabromo-3-hydroxy-6-oxoxanthen-9-yl)benzene-1,3-dicarboxylic acid;2-(2,4,5,7-tetrabromo-3-hydroxy-6-oxoxanthen-9-yl)terephthalic acid
Molecular FormulaC42H16Br8O14
Molecular Weight1383.8
Topological Polar Surface Area242
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count14
Rotatable Bond Count6
Heavy Atom Count64
Formal Charge0
Complexity1920
SMILES
C1=CC(=C(C(=C1)C(=O)O)C2=C3C=C(C(=O)C(=C3OC4=C(C(=C(C=C24)Br)O)Br)Br)Br)C(=O)O.C1=CC(=C(C=C1C(=O)O)C2=C3C=C(C(=O)C(=C3OC4=C(C(=C(C=C24)Br)O)Br)Br)Br)C(=O)O
InChI
InChI=1S/2C21H8Br4O7/c22-11-4-9-13(8-3-6(20(28)29)1-2-7(8)21(30)31)10-5-12(23)17(27)15(25)19(10)32-18(9)14(24)16(11)26;22-10-4-8-13(12-6(20(28)29)2-1-3-7(12)21(30)31)9-5-11(23)17(27)15(25)19(9)32-18(8)14(24)16(10)26/h2*1-5,26H,(H,28,29)(H,30,31)
InChIKey
BEFSXKPEQVWGHQ-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 5(6)-Carboxyeosin
CAS: 132201-84-4
CID: 44119976
Formula: C42H16Br8O14
MW: 1383.8
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight1383.8
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count14
Rotatable Bond Count6
Exact Mass1383.39251
Monoisotopic Mass1375.40071
Topological Polar Surface Area242 Ų
Heavy Atom Count64
Formal Charge0
Complexity1920
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes

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