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56360-46-4

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  • 4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitrospiro[2-benzofuran-3,9'-xanthene]-1-one

    Cas No: 56360-46-4

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  • NovaChemistry
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  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitro-

    Cas No: 56360-46-4

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  • ChemService Inc.
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  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitro-

    Cas No: 56360-46-4

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  • AppliChem GmbH
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  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitro-

    Cas No: 56360-46-4

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  • POLYSCI
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  • Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one,4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitro-

    Cas No: 56360-46-4

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  • City Chemical LLC
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56360-46-4 Usage

Description

EOSIN B is a C-nitro compound characterized by a fluorescein skeleton with bromo groups at positions 4 and 5 and nitro groups at positions 2 and 7. It is an orange powder known for its chemical properties.

Uses

Used in Pharmaceutical Industry:
EOSIN B is used as a staining agent for the detection and visualization of various cellular structures, particularly in histology and cytology. Its fluorescent properties allow for the identification of specific cell types and tissues, aiding in the diagnosis of diseases and understanding cellular processes.
Used in Research Applications:
In the field of research, EOSIN B is utilized as a vital dye for staining cells and tissues in experiments involving cell biology, microbiology, and pathology. Its ability to bind to specific cellular components makes it a valuable tool for studying cell morphology, cell death, and other cellular phenomena.
Used in Textile Industry:
EOSIN B is employed as a dye in the textile industry, where it is used to impart color to fabrics. Its vibrant hue and chemical stability make it a popular choice for various textile applications, including clothing, upholstery, and decorative items.
Used in Analytical Chemistry:
In analytical chemistry, EOSIN B is used as an indicator in acid-base titrations and as a pH-sensitive dye in various assays. Its color change in response to changes in pH allows for the accurate measurement of pH levels in solutions, which is crucial for many chemical analyses and reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 56360-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56360-46:
(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*4)+(1*6)=124
124 % 10 = 4
So 56360-46-4 is a valid CAS Registry Number.

56360-46-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitrospiro[2-benzofuran-3,9'-xanthene]-1-one

1.2 Other means of identification

Product number -
Other names Saffrosine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56360-46-4 SDS

56360-46-4Relevant articles and documents

Novel β-cyclodextrin-eosin conjugates

Benkovics, Gábor,Afonso, Damien,Darcsi, András,Béni, Szabolcs,Conoci, Sabrina,Fenyvesi, éva,Szente, Lajos,Malanga, Milo,Sortino, Salvatore

supporting information, p. 543 - 551 (2017/03/29)

Eosin B (EoB) and eosin Y (EoY), two xanthene dye derivatives with photosensitizing ability were prepared in high purity through an improved synthetic route. The dyes were grafted to a 6-monoamino-β-cyclodextrin scaffold under mild reaction conditions through a stable amide linkage using the coupling agent 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride. The molecular conjugates, well soluble in aqueous medium, were extensively characterized by 1D and 2D NMR spectroscopy and mass spectrometry. Preliminary spectroscopic investigations showed that the β-cyclodextrin-EoY conjugate retains both the fluorescence properties and the capability to photogenerate singlet oxygen of the unbound chromophore. In contrast, the corresponding β-cyclodextrin-EoB conjugate did not show either relevant emission or photosensitizing activity probably due to aggregation in aqueous medium, which precludes any response to light excitation.

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