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(2-hydroxyethyl) hydrogen succinate, also known as succinic acid monoester with 2-hydroxyethanol or ethylene glycol mono(2-hydroxyethyl) succinate, is a chemical compound with the molecular formula C6H10O5. It is a diester of succinic acid, featuring a hydroxyl group in the 2 position and an ester group in the 1 position. This versatile compound serves as a key intermediate in the synthesis of a wide range of products, including pharmaceuticals, polymers, and agricultural products.

21583-38-0

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21583-38-0 Usage

Uses

Used in Chemical Synthesis:
(2-hydroxyethyl) hydrogen succinate is used as an intermediate in the synthesis of various chemicals for its ability to react and form new compounds, contributing to the development of pharmaceuticals, polymers, and agricultural products.
Used in Production of Other Esters:
(2-hydroxyethyl) hydrogen succinate is used as a precursor to produce other esters, highlighting its importance in the chemical industry for creating a variety of ester-based compounds.
Used as a Solvent:
In various industrial applications, (2-hydroxyethyl) hydrogen succinate is used as a solvent due to its ability to dissolve other substances, which is crucial for numerous manufacturing processes.
Used in Surfactant Production:
(2-hydroxyethyl) hydrogen succinate is used as a reactant in the production of surfactants, which are essential for creating products that lower the surface tension of a liquid, facilitating various applications in industries such as detergents and personal care.
Used in Personal Care and Cosmetic Products:
As a component in personal care and cosmetic products, (2-hydroxyethyl) hydrogen succinate contributes to the formulation of creams, lotions, and other beauty products, enhancing their texture, stability, and effectiveness.

Check Digit Verification of cas no

The CAS Registry Mumber 21583-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,8 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21583-38:
(7*2)+(6*1)+(5*5)+(4*8)+(3*3)+(2*3)+(1*8)=100
100 % 10 = 0
So 21583-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O5/c7-3-4-11-6(10)2-1-5(8)9/h7H,1-4H2,(H,8,9)

21583-38-0Downstream Products

21583-38-0Relevant academic research and scientific papers

Preparation of unsaturated polyesters using boric acid as mild catalyst and their sulfonated derivatives as new family of degradable polymer surfactants

Alemdar, Neslihan,Erciyes, A. Tuncer,Bicak, Niyazi

experimental part, p. 5044 - 5050 (2011/11/14)

Boric acid-pyridine mixture is presented as mild catalyst for polycondensation of semi-esters of ethylene glycol, in situ-generated by " cyclic anhydride-diol" reaction scheme from maleic, succinic and phthalic anhydrides. This catalyst system was demonstrated to give colorless polyesters in low molecular weights (Mn: 1650-1950 Da) within 4 h at 130 °C 1H NMR spectra of the polyesters derived from maleic anhydride revealed significant isomerization of maleate groups to fumarate units (~80 %) during the polyesterification. Maleate and fumarate double bonds of the unsaturated polyesters (USP) were demonstrated to add bisulfite ions quantitatively to give sulfonated polyesters. The resulting sulfonated polyesters with 50% and 70% succinate units exhibited relatively narrow size spherical and ellipsoidal micelles in aqueous solutions, as inferred from surface tension, DLS and ESEM measurements. The results showed that, this procedure allows preparing a new family of polymer surfactants with tunable hydrophilicity and degradable polyester backbones.

Synthesis of macrocyclic dilactones through lipases

Bosch, Ma. Pilar,Guerrero, Angel

, p. 2611 - 2614 (2007/10/03)

We report herein a selective and efficient method to prepare macrocyclic dilactones in good yields from diols and succinic anhydride through a biocatalytic condensation reaction. Georg Thieme Verlag Stuttgart.

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