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1,3,5-Benzenetriacetic acid, 2,4,6-triethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220759-05-7

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220759-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220759-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,7,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220759-05:
(8*2)+(7*2)+(6*0)+(5*7)+(4*5)+(3*9)+(2*0)+(1*5)=117
117 % 10 = 7
So 220759-05-7 is a valid CAS Registry Number.

220759-05-7SDS

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 2-[3,5-bis(carboxymethyl)-2,4,6-triethylphenyl]acetic acid

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetriacetic acid,2,4,6-triethyl

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:220759-05-7 SDS

220759-05-7Relevant academic research and scientific papers

A shape-dependent hydrophobic effect for tetrazoles

Mahnke, Devin J.,McDonald, Robert,Hof, Fraser

, p. 3738 - 3740 (2007)

An adaptive tetrazole-derived host provides insight into tetrazolate-biomolecule interactions, and is the first member of a new family of receptors that function in pure water. The Royal Society of Chemistry.

COMPOUNDS AND METHODS FOR CHELATING METALS IN AQUEOUS SOLUTIONS

-

Page/Page column 17-19, (2010/12/26)

The present invention relates to a new class of organic compounds and their use, for example, to sequester metal ions, including actinides (such as uranium and plutonium), precious metals (such as gold, silver and platinum) and all other metals (such as transition metals), from aqueous solutions, such as bodies of water (including but not limited to ocean water, seawater, river water) and all other aqueous solutions. Specifically, the present invention relates to a new class of polydentate organic chelating agents and methods for their use to recover metals from aqueous solutions, such as uranium from seawater.

Selective recognition and extraction of the uranyl ion

Sather, Aaron C.,Berryman, Orion B.,Rebek Jr., Julius

supporting information; experimental part, p. 13572 - 13574 (2010/12/18)

A tripodal receptor capable of extracting uranyl ion from aqueous solutions has been developed. At a uranyl concentration of 400 ppm, the developed ligand extracts ~59% of the uranyl ion into the organic phase. The new receptor features three carboxylates

Synthesis and binding studies of bowl-shaped hosts for quaternary ammoniums

Jeong, Kyu-Sung,Shin, Kwang Hoon,Kim, Soong-Hyun

, p. 1166 - 1167 (2007/10/03)

Two bowl-shaped hosts for quaternary ammonium salts were synthesized and their binding properties, along with the anion effect, were systematically examined and compared in CDCl3.

"Flexiball" toolkit: A modular approach to self-assembling capsules

O'Leary,Szabo,Svenstrup,Schalley,Luetzen,Schaefer,Rebek Jr.

, p. 11519 - 11533 (2007/10/03)

We report the synthesis and characterization of new, self-assembling molecular capsules. The modular strategy makes use of glycoluril building blocks available in multigram amounts combined with aromatic spacer elements. The lengthy syntheses encountered with earlier generations of capsules are avoided, and several capsules of nanometer dimensions are now accessible. Single bond attachments between spacers and glycoluril modules result in monomers as dimeric capsules that are less rigid than their earlier counterparts. The host-guest properties of the homo- and heterodimeric capsules were studied using a combination of NMR and ESI-mass spectrometry. They show a less pronounced selectivity for guests of different sizes, and their increased flexibility prevents self-assembly when no rigidifying elements are present on the central spacer unit. Some of the new capsules bear inwardly directed, secondary amide N-H protons. These can be further functionalized, as shown by their methylation to give tertiary analogues. The structures hold broader implications for the placement of functional groups on concave molecular surfaces.

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