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N,N,N',N'-Tetramethyl-9H-xanthene-3,6-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53510-49-9

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53510-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53510-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,1 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53510-49:
(7*5)+(6*3)+(5*5)+(4*1)+(3*0)+(2*4)+(1*9)=99
99 % 10 = 9
So 53510-49-9 is a valid CAS Registry Number.

53510-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-N,3-N,6-N,6-N-tetramethyl-9H-xanthene-3,6-diamine

1.2 Other means of identification

Product number -
Other names N,N,N',N'-tetramethyl-9H-xanthene-3,6-diamine

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:53510-49-9 SDS

53510-49-9Downstream Products

53510-49-9Relevant academic research and scientific papers

Silicon incorporation in polymethine dyes

Pengshung, Monica,Neal, Patrick,Atallah, Timothy L.,Kwon, Junho,Caram, Justin R.,Lopez, Steven A.,Sletten, Ellen M.

supporting information, p. 6110 - 6113 (2020/06/10)

Methods to red-shift fluorophores have garnered considerable interest due to the broad utility of low energy light. The incorporation of silicon into xanthene and coumarin scaffolds has resulted in an array of visible and near-infrared fluorophores. Here,

Improved Xanthone Synthesis, Stepwise Chemical Redox Cycling

Bachman, James L.,Escamilla, P. Rogelio,Boley, Alexander J.,Pavlich, Cyprian I.,Anslyn, Eric V.

supporting information, p. 206 - 209 (2019/01/10)

A base-catalyzed direct oxidation of rhodamine, carborhodamine, and siliconrhodamine pyronines to the corresponding xanthones is studied. This methodology utilizes addition of water to split pyronines into xanthone and reduced xanthene, the latter of whic

CalFluors: A Universal Motif for Fluorogenic Azide Probes across the Visible Spectrum

Shieh, Peyton,Dien, Vivian T.,Beahm, Brendan J.,Castellano, Joseph M.,Wyss-Coray, Tony,Bertozzi, Carolyn R.

supporting information, p. 7145 - 7151 (2015/06/25)

Fluorescent bioorthogonal smart probes across the visible spectrum will enable sensitive visualization of metabolically labeled molecules in biological systems. Here we present a unified design, based on the principle of photoinduced electron transfer, to access a panel of highly fluorogenic azide probes that are activated by conversion to the corresponding triazoles via click chemistry. Termed the CalFluors, these probes possess emission maxima that range from green to far red wavelengths, and enable sensitive biomolecule detection under no-wash conditions. We used the CalFluor probes to image various alkyne-labeled biomolecules (glycans, DNA, RNA, and proteins) in cells, developing zebrafish, and mouse brain tissue slices.

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