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76-54-0 Usage

Description

2',7'-DICHLOROFLUORESCEIN is a widely used fluorescent probe with various applications in analytical chemistry, biochemistry, and cell biology. It is known for its ability to detect and measure different analytes, such as carbohydrates and hydrogen peroxide, through fluorescence densitometry and chemiluminescence. Additionally, it serves as an indicator in argentometry by the Fajans method and is involved in cellular antioxidant activity assays. Its fluorescent properties also make it a valuable additive in fluorescence and laser studies.

Uses

Used in Analytical Chemistry:
2',7'-DICHLOROFLUORESCEIN is used as a fluorescent probe for the determination of carbohydrates and hydrogen peroxide by fluorescence densitometry and chemiluminescence, respectively. This allows for sensitive and selective detection of these analytes in various samples.
Used in Biochemistry:
In biochemistry, 2',7'-DICHLOROFLUORESCEIN is used as an indicator for argentometry by the Fajans method, which is a technique for detecting and measuring the presence of silver ions in a solution.
Used in Cell Biology:
2',7'-DICHLOROFLUORESCEIN is used as a cellular antioxidant activity indicator, helping to assess the antioxidant capacity of cells and their ability to neutralize reactive oxygen species.
Used in Fluorescence and Laser Studies:
Due to its fluorescent properties, 2',7'-DICHLOROFLUORESCEIN is utilized as an additive in fluorescence and laser studies, contributing to the development of new fluorescent sensors and imaging techniques.
Used in Environmental and Biological Imaging:
A new fluorescent sensor for Cd2+ has been developed using 2',7'-DICHLOROFLUORESCEIN, which has potential applications in living cells imaging, as reported in Tetrahedron Lett. 2015, 56 (11), 1322-1327.
Used in Detection of Fluoride Ions:
2',7'-DICHLOROFLUORESCEIN has been employed in the colorimetric and fluorogenic signaling of fluoride ions, as described in Dyes Pigm. 2015, 112, 170-175, which can be useful in environmental monitoring and analysis.

Biological Activity

2',7'-dichlorofluorescein is an oxidation-sensitive fluorescent probe. 2′7′-dichlorofluorescein diacetate is oxidized to 2′7′-dichlorofluorescein in the presence of ROS (reactive oxygen species).

Biochem/physiol Actions

2′,7′-Dichlorofluorescein is an oxidation-sensitive fluorescent probe. 2′7′-dichlorofluorescein diacetate is oxidized to 2′7′-dichlorofluorescein in the presence of ROS (reactive oxygen species).

Check Digit Verification of cas no

The CAS Registry Mumber 76-54-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76-54:
(4*7)+(3*6)+(2*5)+(1*4)=60
60 % 10 = 0
So 76-54-0 is a valid CAS Registry Number.

76-54-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D0371)  2',7'-Dichlorofluorescein [for Fluorescent indicator]  >95.0%(HPLC)

  • 76-54-0

  • 1g

  • 160.00CNY

  • Detail
  • TCI America

  • (D0371)  2',7'-Dichlorofluorescein [for Fluorescent indicator]  >95.0%(HPLC)

  • 76-54-0

  • 25g

  • 1,330.00CNY

  • Detail
  • Alfa Aesar

  • (A16212)  2',7'-Dichlorofluorescein   

  • 76-54-0

  • 5g

  • 430.0CNY

  • Detail
  • Alfa Aesar

  • (A16212)  2',7'-Dichlorofluorescein   

  • 76-54-0

  • 25g

  • 1389.0CNY

  • Detail
  • Fluka

  • (02591)  2′,7′-Dichlorofluoresceinsolution  indicator, ready-to-use

  • 76-54-0

  • 02591-500ML

  • 1,334.97CNY

  • Detail

76-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',7'-dichlorofluorescein

1.2 Other means of identification

Product number -
Other names Spiro[isobenzofuran-1(3H),9‘-[9H]xanthen]-3-one, 2‘,7‘-dichloro-3‘,6‘-dihydroxy-

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:76-54-0 SDS

76-54-0Relevant articles and documents

Regulative peroxidase activity of DNA-linked hemin by graphene oxide for fluorescence DNA sensing

Wang, Quanbo,Xu, Nan,Lei, Jianping,Ju, Huangxian

, p. 6714 - 6717 (2014)

The inhibition effect of graphene oxide toward the peroxidase activity of DNA-linked hemin was identified and conveniently utilized in the design of a homogenous fluorescence strategy for DNA sensing with high sensitivity. This journal is the Partner Organisations 2014.

Metal-binding and redox properties of substituted linear and cyclic ATCUN motifs

Neupane, Kosh P.,Aldous, Amanda R.,Kritzer, Joshua A.

, p. 65 - 76 (2014)

The amino-terminal copper and nickel binding (ATCUN) motif is a short peptide sequence found in human serum albumin and other proteins. Synthetic ATCUN-metal complexes have been used to oxidatively cleave proteins and DNA, cross-link proteins, and damage cancer cells. The ATCUN motif consists of a tripeptide that coordinates Cu(II) and Ni(II) ions in a square planar geometry, anchored by chelation sites at the N-terminal amine, histidine imidazole and two backbone amides. Many studies have shown that the histidine is required for tight binding and square planar geometry. Previously, we showed that macrocyclization of the ATCUN motif can lead to high-affinity binding with altered metal ion selectivity and enhanced Cu(II)/Cu(III) redox cycling (Inorg. Chem. 2013, 52, 2729-2735). In this work, we synthesize and characterize several linear and cyclic ATCUN variants to explore how substitutions at the histidine alter the metal-binding and catalytic properties. UV-visible spectroscopy, EPR spectroscopy and mass spectrometry indicate that cyclization can promote the formation of ATCUN-like complexes even in the absence of imidazole. We also report several novel ATCUN-like complexes and quantify their redox properties. These findings further demonstrate the effects of conformational constraints on short, metal-binding peptides, and also provide novel redox-active metallopeptides suitable for testing as catalysts for stereoselective or regioselective oxidation reactions.

G-quadruplex DNAzyme as the turn on switch for fluorimetric detection of genetically modified organisms

Qiu, Bin,Zheng, Zhen-Zhu,Lu, Yu-Jing,Lin, Zhen-Yu,Wong, Kwok-Yin,Chen, Guo-Nan

, p. 1437 - 1439 (2011)

A novel fluorescent sensor for detection of genetically modified organisms was developed, and in the sensor G-quadruplex DNAzyme (G-quadruplex-hemin complex) was used as the turn on switch.

Pyrocatalytic oxidation-strong size-dependent poling effect on catalytic activity of pyroelectric BaTiO3nano- And microparticles

Braeutigam, Patrick,Buchheim, Johannes R.,Neumeister, Peter,Raufeisen, Sascha,Stelter, Michael

, p. 23464 - 23473 (2020/11/18)

Pyrocatalysis is an emerging advanced oxidation process for wastewater remediation with the potential for thermal energy harvesting and utilization. Although several studies explored the potential of new pyrocatalyst materials to degrade harmful organic water pollutants, the role of important material properties and electric poling procedures on the pyrocatalytic activity is still unclear. In this work, we investigate the interdependence between particle size, electric poling and pyrocatalytic activity of BaTiO3 powders with nominal particle sizes of 100, 200 and 500 nm by using the dichlorofluorescein redox assay. Depending on the particle size, the influence of surface area or phase composition on the pyrocatalytic activity predominates. Moreover, we demonstrate that poling of pyrocatalysts leads to a strong size-dependent increase of pyrocatalytic activity. This poling effect increases with particle size up to +247% and can be explained with size-dependent changes in phase composition and domain structure. Combining all results, the progression of the pyrocatalytic activity as a function of particle size was derived and a future strategy for maximizing the catalytic performance of pyrocatalysts was developed. This study greatly improves the understanding about the role of important material properties and electric poling on pyrocatalytic activity, thus enabling an effective catalyst design. With the help of highly active catalysts, the pyrocatalytic process can take the next step in its development into a new and energy-efficient advanced oxidation process for water remediation.

Ti(IV) doping: An effective strategy to boost Lewis acidic performance of ZnO catalyst in fluorescein dye synthesis

Jadhav, Nirajkumar H.,Shinde, Dnyaneshwar R.,Sakate, Sachin S.,Rasal, Nishant K.,Pawar, Ramdas A.

, p. 17 - 22 (2018/11/25)

Zn1-xTixO NPs were efficiently synthesized using a simple solution free mechanochemical method. The synthesized ZnO and Ti(IV)-doped ZnO catalysts are exhibited polycrystallinity, a hexagonal crystal structure, and roughly spherical agglomerates. The surface areas of the Zn1-xTixO catalysts were positively correlated with the doping percentage of Ti(IV), which also enhanced the Lewis acidity of the NPs. The catalysts exhibited excellent activity during the synthesis of fluorescein dyes. This methodology was also extended to sulfone-fluorescein dye synthesis.

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