Eosin Staining Solution - 5%(w/v) , CAS No.17372-87-1

CAS: 17372-87-1 Cat. No.: E196384 Formula: C20H6Br4Na2O5 Peso molecolare: 691.85 Numero EC: 241-409-6
Disponibile su ordine
QUALITÀ & PUREZZA 5%(w/v)
Synonyms
Eosine Extra Yellowish | Eosine Lake Red Y | Eosine Yellowish | Eosin Natricum | Fenazo Eosine XG | Phloxine Toner B | Bromo 4DL | C.I. Acid Red 87 | Bromo X-100 | Bromo 4D | Fluorescein, 2',4',5',7'-tetrabromo-, disodium salt | TDQ283MPCW | Tetrabromoflu
Storage
Protected from light,Room temperature
Shipped In
Normal
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
100ml
E196384-100ml
—
4 Disponibile
78,01€
Enter a quantity for the sizes you want to add.

Panoramica

Eosin, also known as eosin, is a xanthene dye in synthetic dyes. It is a pink or pink powder. Eosin is most suitable for staining with hematoxylin to show the morphological structure of normal or pathological tissues. Water soluble eosin Y contains a chromophore of quinone type benzene ring and two acidic chromophores (r-coona, r-ona) that form sodium salt. This salt forming acidic dye dissociates into negatively charged chromo acid moieties (r-coo, r-o-) when dissolved in water, that is, the colored part of the dye and the positively charged sodium ion part (na+). When staining, the negatively charged tryptophan part of Eosin Y combines with the positively charged substances in the tissue in the form of ionic bonds to develop color. Eosinystain is a special preservative, which is simple to operate and does not use toxic reagents such as mercury and methanol. It can be used for staining tissue sections or cultured cells. It can be used with immunofluorescence staining or immunohistochemical staining. On the one hand, it can be stained with immunofluorescence or other dyes after eosin staining, on the other hand, it can also be counterstained with eosin after immunohistochemical staining. This staining solution can be reused until the effect is considered to be poor, and then use a new staining solution. After staining, the cell plasma is pink or red.
Self prepared materials: 1. Distilled water 2. 4% paraformaldehyde 3. Series of ethanol
Operation steps (for reference only):
1. Sample processing a) for paraffin sections: dewaxing in xylene. Use fresh xylene and dewax. b) For frozen sections: distilled water for 2min. c) For cultured cells: fixed with paraformaldehyde. Wash with distilled water. Change to fresh distilled water and wash again.
2. Eosin staining for the above treated samples, eosin staining solution shall be used for 0.5~2min (the time shall be adjusted according to the staining results and requirements). If direct observation is needed, it can be washed twice with 70% ethanol. If dehydration, transparency and sealing are required, follow the subsequent steps. After washing with 70% ethanol, dehydration, transparency and sealing can still be carried out according to the subsequent steps. Note: if it is used for counterstaining after immunohistochemical staining, refer to the above steps to carry out eosin staining after other staining.
3. Dehydration, transparency, sealing or other staining a) dehydration, transparency, sealing: replace ethanol dehydration with fresh ethanol for dehydration. Xylene is transparent. Use fresh xylene and make it transparent again. Seal the film with neutral gum or other sealing agent. Under the microscope, the cytoplasm was pink or red. b) Other staining: if immunofluorescence staining or Hoechst and other fluorescent dyes are used, wash with ethanol after staining with eosin staining solution. PBS or normal saline or TBS or tbst and other solutions for immunostaining or fluorescent dye staining. Perform immunofluorescence staining or staining with other fluorescent dyes.
Precautions:
1. If dehydration, transparency and sealing treatment are required, xylene, neutral gum or other sealing agents shall be prepared by yourself. If the sample is paraffin sectioned, 90% ethanol, absolute ethanol and xylene should be prepared by yourself.
2. For your safety and health, please wear lab clothes and disposable gloves.
3. This product is for scientific research use only, and other uses are strictly prohibited.

Specifiche

Sinonimi
Eosine Extra Yellowish | Eosine Lake Red Y | Eosine Yellowish | Eosin Natricum | Fenazo Eosine XG | Phloxine Toner B | Bromo 4DL | C.I. Acid Red 87 | Bromo X-100 | Bromo 4D | Fluorescein, 2',4',5',7'-tetrabromo-, disodium salt | TDQ283MPCW | Tetrabromoflu
Specifiche e purezza
5%(w/v)
Condizioni di conservazione di stoccaggio
Protected from light,Room temperature
Spedito in
Normal
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488181248
Isomeri SMILES
C1=CC=C(C(=C1)C2=C3C=C(C(=O)C(=C3OC4=C(C(=C(C=C24)Br)[O-])Br)Br)Br)C(=O)[O-].[Na+].[Na+]
CAS alternativo
152-75-0
Peso molecolare
691.85

Dati avanzati

Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDataOggetto
K2113114K2113114Certificate of AnalysisAug 13, 2025 E196384
H2515278H2515278Certificate of AnalysisJul 04, 2025 E196384
D2306317D2306317Certificate of AnalysisFeb 17, 2023 E196384
D2306319D2306319Certificate of AnalysisFeb 17, 2023 E196384
Proprietà chimiche e fisiche
SolubilitàSoluble in water, fairly soluble in alcohol, insoluble in ether
SensibilitàLight sensitive
Peso molecolare691.900 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count1
Exact Mass691.67 Da
Monoisotopic Mass687.674 Da
Topological Polar Surface Area89.500 Ų
Heavy Atom Count31
Formal Charge0
Complexity796.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Domande frequenti e articoli
Visible Light Photoredox Catalysts
Photo-Crosslinking and Patterning of PEG-Based Hydrogels (2D/3D): Principles, Method Comparisons, and Product Selection Guidelines
Giemsa Staining Protocol: Peripheral Blood and Bone Marrow Smears
Methodological essentials for mineralization visualization: Alizarin Red S staining vs. Von Kossa silver staining
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Applications and Comparison of Histological Counterstaining, Collagen Evaluation, and Protein Staining Methods
How Degradable Poly(ethylene glycol) Hydrogels Build Tunable Cellular Microenvironments: Adhesion, Degradation, Release, and Experimental Interpretation in 2D/3D Culture
How Degradable Poly(ethylene glycol) Hydrogels Build Tunable Cellular Microenvironments: Adhesion, Degradation, Release, and Experimental Interpretation in 2D/3D Culture
Designing Hydrogel Scaffolds as Programmable Cell Microenvironments: From Click-Chemistry Functionalization to 3D Cell Culture Experimental Design
Functional Distinction among Orange G-6, EA36, and EA50 in the Papanicolaou Staining System
Types, Binding Mechanisms, and Experimental Selection of Nuclear Dyes
Romanowsky Staining Systems: Chromogenic Basis, Method Types, and Result Interpretation
Eosinophil Morphological Observation: Staining Basis, Identification Points, and Research Validation
Mechanism of Action and Selection Logic of Photoinitiators
Color-Development Mechanisms, Formulation Forms, and Selection/Application Logic of Colorants in Personal Care Products
Neuropathological Mechanisms of Cerebral Infarction
Establishment and Evaluation Methods of Diabetic Animal Models
Histological Staining Methods for Identifying Hepatitis B Virus: Comparison of HE, Orcein, Aldehyde Fuchsin, Victoria Blue, Immunohistochemistry, and In Situ Hybridization
Establishment and Application of Animal Models of Bladder Cancer (BC)
Establishment and Application of Animal Models of Epilepsy (EP)
Establishment and Evaluation of Animal Models of Acute Kidney Injury (AKI/ARF)
Summary of Cell Staining Methods
Where Does the Selectivity in Piperidine C–H Functionalization Come From? — Nitrogen Effects, Chair Conformations, and Four Classes of Key Intermediates
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Desidera che le inviamo un messaggio quando avremo sconti disponibili?

Ricordamelo più tardi

Grazie! Controlli la sua casella di posta per confermare.

Ops! Le notifiche sono disabilitate.