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3348-03-6

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3348-03-6 Usage

Description

6-CARBOXYFLUORESCEIN DIACETATE (6-CFDA) is a fluorescent probe that is widely utilized in various applications due to its unique properties. It is a polyanionic compound that can be used to differentiate viable cells from apoptotic cells, as well as to detect changes in intracellular pH. 6-CARBOXYFLUORESCEIN DIACETATE is particularly useful in the field of cell biology and molecular biology, providing valuable insights into cellular processes and functions.

Uses

Used in Cell Biology:
6-CARBOXYFLUORESCEIN DIACETATE is used as a cell viability indicator for distinguishing between viable and apoptotic cells. The expression is: 6-CARBOXYFLUORESCEIN DIACETATE is used as a cell viability indicator for [distinguishing viable cells from apoptotic cells] because [live cells that are not apoptotic accumulate 6-carboxyfluorescein but do not accumulate annexin].
Used in Molecular Biology:
6-Carboxyfluorescein Diacetate is used as a fluorescent probe for detecting changes in intracellular pH. The expression is: 6-CARBOXYFLUORESCEIN DIACETATE is used as a fluorescent probe for [detecting changes in intracellular pH] because [it is a polyanionic compound that can be used to monitor pH variations within cells].
Used in Flow Cytometry:
6-Carboxyfluorescein Diacetate derivatives can be used as staining agents for flow cytometry to visualize cells undergoing apoptosis or necrosis. The expression is: 6-CARBOXYFLUORESCEIN DIACETATE is used as a staining agent for [visualizing cells undergoing apoptosis or necrosis] in the context of [flow cytometry] because [its derivatives can be used to specifically label and identify these cells].

Check Digit Verification of cas no

The CAS Registry Mumber 3348-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3348-03:
(6*3)+(5*3)+(4*4)+(3*8)+(2*0)+(1*3)=76
76 % 10 = 6
So 3348-03-6 is a valid CAS Registry Number.
InChI:InChI=1/C25H16O9/c1-12(26)31-15-4-7-18-21(10-15)33-22-11-16(32-13(2)27)5-8-19(22)25(18)20-9-14(23(28)29)3-6-17(20)24(30)34-25/h3-11H,1-2H3,(H,28,29)

3348-03-6SDS

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 6-CARBOXYFLUORESCEIN DIACETATE

1.2 Other means of identification

Product number -
Other names 6-CARBOXY-DI-O-ACETYLFLUORESCEIN

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:3348-03-6 SDS

3348-03-6Relevant articles and documents

Separating the isomers - Efficient synthesis of the N-hydroxysuccinimide esters of 5 and 6-carboxyfluorescein diacetate and 5 and 6-carboxyrhodamine B

Brunet, Aurlie,Aslam, Tashfeen,Bradley, Mark

, p. 3186 - 3188 (2014)

Diacetate protection of 5 and 6-carboxyfluorescein followed by synthesis of the N-hydroxysuccinimide esters allowed ready separation of the two isomers on a multi-gram scale. The 5 and 6-carboxyrhodamine B N-hydroxysuccinimide esters were also readily synthesised and separated.

Site-specific, reversible and fluorescent immobilization of proteins on CrAsH-modified surfaces for microarray analytics

Schulte-Zweckel, Janine,Rosi, Federica,Sreenu, Domalapally,Schr?der, Hendrik,Niemeyer, Christof M.,Triola, Gemma

supporting information, p. 12761 - 12764 (2015/05/20)

A novel technique for protein immobilization onto CrAsH-modified surfaces is presented. This approach enables an efficient, reversible and fluorogenic immobilization of proteins. Moreover, expressed proteins can also be directly immobilized from cellular lysates without prior purification. The immobilized proteins are suitable for protein-protein interaction studies and the fluorescence enhancement upon immobilization can be employed for the direct detection of the immobilized protein without the need for secondary detection methods. This journal is

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