10283-83-7

Basic information

• Product Name: bis(2-hydroxyethyl) succinate
• Synonyms: bis(2-hydroxyethyl) succinate;Butanedioic acid bis(2-hydroxyethyl) ester;Einecs 233-631-7
• CAS NO: 10283-83-7
• Molecular Formula: C₈H₁₄O₆
• Molecular Weight: 206.19316
• EINECS: 233-631-7
• Mol File: 10283-83-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 360 °C at 760 mmHg
• Flash Point: 142.6 °C
• Appearance: /
• Density: 1.268 g/cm³
• Vapor Pressure: 1.23E-06mmHg at 25°C
• Refractive Index: 1.474
• PKA: 13.57±0.10(Predicted)
• CAS DataBase Reference: bis(2-hydroxyethyl) succinate(CAS DataBase Reference)
• NIST Chemistry Reference: bis(2-hydroxyethyl) succinate(10283-83-7)
• EPA Substance Registry System: bis(2-hydroxyethyl) succinate(10283-83-7)

Safety Data

• Hazardous Substances Data: 10283-83-7(Hazardous Substances Data)

Usage

General Description

Bis(2-hydroxyethyl) succinate is a chemical compound that is used in various industrial and commercial applications. It is a diester of succinic acid and is composed of two hydroxyethyl groups attached to the succinate molecule. This chemical is commonly used as a plasticizer, which means it is added to plastics to make them more flexible and easier to process. It is also used in the production of resins, adhesives, and coatings. Additionally, bis(2-hydroxyethyl) succinate can be found in personal care products, such as cosmetics and lotions, where it acts as a conditioning agent and emollient. Due to its versatile applications, this chemical is widely used in the manufacturing of everyday products and materials.

InChI:InChI=1/C8H14O6/c9-3-5-13-7(11)1-2-8(12)14-6-4-10/h9-10H,1-6H2

Upstream product

• 75-21-8 oxirane 
• 110-15-6 succinic acid 
• 107-21-1 ethylene glycol 

Relevant articles and documents

THERAPEUTIC PROTEIN COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME

Disclosed herein are compositions and methods for preparation and use of protein therapeutics, and more particularly protein clusters or backpacks having a plurality of therapeutic protein monomers reversibly crossed-linked by biodegradable linkers.

Structure-mechanochemical activity relationships for cyclobutane mechanophores

Ultrasound activation of mechanophores embedded in polymer backbones has been extensively studied of late as a method for realizing chemical reactions using force. To date, however, there have been few attempts at systematically investigating the effects of mechanophore structure upon rates of activation by an acoustic field. Herein, we develop a method for comparing the relative reactivities of various cyclobutane mechanophores. Through the synthesis and ultrasonic irradiation of a molecular weight series of poly(methyl acrylate) polymers in which each macromolecule has a single chain-centered mechanophore, we find measurable and statistically significant shifts in molecular weight thresholds for mechanochemical activation that depend on the structure of the mechanophore. We also show that calculations based on the constrained geometries simulate external force method reliably predict the trends in mechanophore reactivity. These straightforward calculations and the experimental methods described herein may be useful in guiding the design and the development of new mechanophores for targeted applications.