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Trisodium (carboxylatomethoxy)succinate, also known as sodium carboxymethoxysuccinate or sodium succinate, is a synthetic organic compound commonly used as a chelating agent in various applications. It is a white crystalline powder that is soluble in water and has the chemical formula C6H6Na3O7. trisodium (carboxylatomethoxy)succinate is derived from succinic acid and contains a carboxyl group and a methoxy group, which contribute to its chelating properties. Trisodium (carboxylatomethoxy)succinate is widely used in detergents, water treatment, and industrial processes to sequester metal ions, preventing them from interfering with the desired reactions or causing unwanted side effects. Its ability to bind with metal ions makes it an effective stabilizer and corrosion inhibitor, enhancing the performance and longevity of products in which it is incorporated.

34128-01-3

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34128-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34128-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,2 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34128-01:
(7*3)+(6*4)+(5*1)+(4*2)+(3*8)+(2*0)+(1*1)=83
83 % 10 = 3
So 34128-01-3 is a valid CAS Registry Number.

34128-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trisodium,2-(carboxylatomethoxy)butanedioate

1.2 Other means of identification

Product number -
Other names EINECS 251-838-0

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:34128-01-3 SDS

34128-01-3Downstream Products

34128-01-3Relevant academic research and scientific papers

Lanthanide(III)-catalysed addition of glycolate to maleate. Investigation of intermediates using multinuclear magnetic resonance spectroscopy

Van Westrenen, Jeroen,Peters, Joop A.,Kieboom, Antonius P. G.,Van Bekkum, Herman

, p. 2723 - 2728 (2007/10/02)

The lanthanum(III)-catalysed addition of glycolate to maleate to yield carboxymethoxysuccinate(3-) (cmos) is described. It is shown that the reaction only proceeds above pH 6, indicating the formation of di-ionised glycolate as a pre-equilibrium for the rate-limiting step, i.e. the addition of the CH2-O- to the olefinic bond. Due to strong complexation of LaIII by the product cmos, the reaction requires one LaIII ion per two cmos formed. The inhibitory effects of non-reacting strong chelators such as ethylenediaminetetra-acetate, nitrilotriacetate, and 2,6-pyridinedicarboxylate indicate the formation of mixed-ligand complexes leading to the addition reaction. This has been confirmed by GdIII-induced 13C relaxation rate enhancements, and DyIII-induced 17O shift measurements.

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