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128924-91-4

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128924-91-4 Usage

Explanation

Different sources of media describe the Explanation of 128924-91-4 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. This is the full name of the compound, which describes its structure and composition.
3. Chelating agent
3. A chelating agent is a molecule that can form multiple bonds with a single metal ion, effectively trapping it.
4. The compound is capable of forming stable complexes with these specific metal ions, which is useful in various applications.
5. Complex structure and functional groups
5. The compound's structure and functional groups, such as the 4-nitrobenzyl group and the tetraacetic acid groups, contribute to its ability to effectively trap metal ions.
6. Due to its ability to bind metal ions, the compound can be used in these fields to improve imaging techniques, deliver drugs more effectively, and detect metal ions in various samples.
7. 4-nitrobenzyl group
7. This functional group is attached to the tetraazacyclotridecane core, providing increased stability and selectivity towards certain metal ions.
8. Versatile tool in biological and chemical research
8. The compound's ability to bind various metal ions and its stability make it a valuable tool for researchers in both biology and chemistry.

Chemical compound

12-(4-nitrobenzyl)-1,4,7,10-tetraazacyclotridecane-1,4,7,10-tetraacetic acid

Binds to metal ions

Calcium, copper, and zinc

Applications

Medical imaging, drug delivery, and metal ion detection

Check Digit Verification of cas no

The CAS Registry Mumber 128924-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128924-91:
(8*1)+(7*2)+(6*8)+(5*9)+(4*2)+(3*4)+(2*9)+(1*1)=154
154 % 10 = 4
So 128924-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H35N5O10/c30-21(31)14-25-5-6-26(15-22(32)33)8-10-28(17-24(36)37)13-19(12-27(9-7-25)16-23(34)35)11-18-1-3-20(4-2-18)29(38)39/h1-4,19H,5-17H2,(H,30,31)(H,32,33)(H,34,35)(H,36,37)

128924-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1,7,10-tris(carboxymethyl)-12-[(4-nitrophenyl)methyl]-1,4,7,10-tetrazacyclotridec-4-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 12-Nbtcta

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:128924-91-4 SDS

128924-91-4Downstream Products

128924-91-4Relevant articles and documents

Accelerating water exchange for GDIII chelates by steric compression around the water binding site

Ruloff, Robert,Toth, Eva,Scopelliti, Rosario,Tripier, Raphael,Handel, Henri,Merbach, Andre E.

, p. 2630 - 2631 (2007/10/03)

The water exchange process was accelerated for nine-coordinate, monohydrated macrocyclic GdIII complexes by inducing steric compression around the water binding site; the increased steric crowding was achieved by replacing an ethylene bridge of

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