925-16-6

Basic information

• Product Name: DIALLYL SUCCINATE
• Synonyms: Butanedioic acid, di-2-propenyl ester;butanedioicacid,di-2-propenylester;JF 2777;JF 3958;Succinic acid, diallyl ester;DIALLYL SUCCINATE;Butanedioic acid diallyl ester;diprop-2-enyl butanedioate
• CAS NO: 925-16-6
• Molecular Formula: C₁₀H₁₄O₄
• Molecular Weight: 198.22
• EINECS: 213-115-8
• Product Categories: Allyl Monomers;Monomers;Polymer Science
• Mol File: 925-16-6.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 105 °C3 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.051 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0108mmHg at 25°C
• Refractive Index: n20/D 1.454(lit.)
• Storage Temp.: Room Temperature
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: DIALLYL SUCCINATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIALLYL SUCCINATE(925-16-6)
• EPA Substance Registry System: DIALLYL SUCCINATE(925-16-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 925-16-6(Hazardous Substances Data)

Usage

Description

Diallyl Succinate is a chemical compound derived from the esterification of succinic acid with allyl alcohol. It is a colorless liquid with a pungent odor and is soluble in water and organic solvents. Due to its unique chemical structure, it has found various applications in different industries.

Uses

Used in Polymer Synthesis:
Diallyl Succinate is used as a monomer in the synthesis of crosslinked polymers. Its reactive allyl groups allow for the formation of covalent bonds with other monomers, resulting in the creation of three-dimensional polymer networks with improved mechanical properties and stability.
Used in Gene Transfection:
Diallyl Succinate is used in the formation of magnetic polyethylenamine complexes for enhancing gene transfection. The magnetic properties of these complexes enable efficient separation and purification of genetic materials, while the polyethylenamine component facilitates the delivery of genes into target cells, improving the efficiency of gene transfection processes.

InChI:InChI=1/C10H14O4/c1-3-7-13-9(11)5-6-10(12)14-8-4-2/h3-4H,1-2,5-8H2

Upstream product

• 110-15-6 succinic acid 
• 107-18-6 allyl alcohol 
• 999-21-3 diallyl maleate 
• 106-95-6 allyl bromide 
• 107-05-1 3-chloroprop-1-ene 
• 108-30-5 succinic acid anhydride 

Downstream Products

• 136286-18-5 2,5-dioxo-cyclohexane-1,4-dicarboxylic acid diallyl ester 
• 193023-50-6 diallyl 2-benzoylsuccinate 
• 71324-09-9 diallyl 2,5-dihydroxycyclohexa-1,4-diene-1,4-dicarboxylate 
• 30273-32-6 2-chloro-3-(2-chlorophenyl)propyl 3-carballyloxypropionate 

Relevant articles and documents

A biocompatible arginine-based polycation

Self assembly between cations and anions is ubiquitous throughout nature. Important biological structures such as chromatin often use polyvalent assembly between a polycation and a polyanion. The biomedical importance of synthetic polycations arises from their affinity to polyanions such as nucleic acid and heparan sulfate. However, the limited biocompatibility of synthetic polycations hampers the realization of their immense potential. By examining biocompatible cationic peptides, we hypothesize that a biocompatible polycation should be biodegradable and made from endogenous cations. We design an arginine-based biodegradable polycation and demonstrate that it is more compatible by several orders of magnitude than conventional polycations in vitro and in vivo. This biocompatibility diminishes when L-arginine is substituted with D-arginine or when the biodegradable ester linker is changed to a biostable ether linker. We believe that this design can lead to many biocompatible polycations that can significantly advance a wide range of applications including controlled release, tissue engineering, biosensing, and medical devices. The design of PAGS and the control polymers that probe the importance of endogenous cations and their degradability in terms of biocompatibility is studied. The biocompatibility is shown to diminish when L-arginine is substituted with D-arginine or when the biodegradable ester linker is changed to a biostable ether linker.

Polymer particles

Biodegradable, cross-linked polymer particle embolics and methods of making the same are described. The particle embolics can be used as embolization agents.

Synthesis and characterization of a new hydroxyl functionalized diacidic ionic liquid as catalyst for the preparation of diester plasticizers

Two new functionalized diacidic ionic liquids (FDAILs) including hydroxyl functionalized diacidic ionic liquid (HFDAIL) and sulfonated diacidic ionic liquid (SFDAIL) were synthesized and characterized by 1HNMR, 13CNMR and FT-IR. The catalytic activities of these FDAILs were examined in esterification reaction of anhydrides with some alcohols to give corresponding dialkyl plasticizers under solvent-free conditions. The results indicate that HFDAIL, as hydroxyl-bearing catalyst, show better catalytic performance. Under the optimum conditions, using HFDAIL, the conversion of phthalic anhydride was high and diester plasticizers were obtained with good to excellent yields in the presence of only 10?mol% of ionic liquid. All the produced diesters could be easily recovered due to their immiscibility with the ionic liquid. Recycling experiments suggests that these ionic liquids can be reused several times without remarkable loss in their catalytic activity.