4074-88-8

Basic information

• Product Name: Diethylene glycol diacrylate
• Synonyms: DIETHYLENE GLYCOL DIACRYLATE;2-Propenoicacid,oxydi-2,1-ethanediylester;acrylicacid,2-ethoxyethanoldiester;acrylicacid,oxydiethyleneester;diacrylatediethyleneglycol;oxydiethyleneacrylate;oxydiethylenediacrylate;tga2
• CAS NO: 4074-88-8
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.22
• EINECS: 223-791-6
• Product Categories: monomer;C10 to C11Materials Science;Biocompatible/Biodegradable Materials;Carbonyl Compounds;Crosslinking AgentsPolymer Science;Esters;Homobifunctional PEGs;Poly(ethylene glycol) and Poly(ethylene oxide);Biomaterials;Acrylate;Building Blocks;C10 to C11;Carbonyl Compounds;Chemical Synthesis;Crosslinking Agents;Homobifunctional PEGs;Materials Science;Organic Building Blocks;Poly(ethylene glycol) and Poly(ethylene oxide);Polymer Science
• Mol File: 4074-88-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: >200℃/760mm
• Boiling Point: 162 °C(lit.)
• Flash Point: >230 °F
• Appearance: colourless liquid
• Density: 1.118 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00201mmHg at 25°C
• Refractive Index: n20/D 1.463(lit.)
• Water Solubility: Slightly soluble in water (1-5g/100ml at 18°C).
• Stability: Stable. Incompatible with radical initiators, strong oxidizing agents, reducing agents, peroxides. Light sensitive. Polymerizes
• BRN: 1953711
• CAS DataBase Reference: Diethylene glycol diacrylate(CAS DataBase Reference)
• NIST Chemistry Reference: Diethylene glycol diacrylate(4074-88-8)
• EPA Substance Registry System: Diethylene glycol diacrylate(4074-88-8)

Safety Data

• Hazard Codes: T
• Statements: 24-36/38-43
• Safety Statements: 28-39-45
• RIDADR: UN 2922 8/PG 3
• WGK Germany: 1
• RTECS: AS9450000
• TSCA: Yes
• HazardClass: 6.1
• PackingGroup: II
• Hazardous Substances Data: 4074-88-8(Hazardous Substances Data)

Usage

Chemical Properties

colourless liquid

Uses

Different sources of media describe the Uses of 4074-88-8 differently. You can refer to the following data:
1. Diethyleneglycol diacrylate is a cross-linking acrylate monomer for use in coatings, adhesives, and printing plates of prepolymer type.
2. Diethylene glycol diacrylate is used as reactive diluent and cross linking agent of radiation curing system, and also may be used as crosslinking resins, plastics and rubber modifier.

General Description

Clear colorless liquid with a mild musty odor.

Air & Water Reactions

Water soluble.

Reactivity Profile

Diethylene glycol diacrylate polymerizes at high temperatures. Diethylene glycol diacrylate is sensitive to light. Diethylene glycol diacrylate is incompatible with strong oxidizers, reducers, peroxides and other radical initiators.

Fire Hazard

Diethylene glycol diacrylate is combustible.

InChI:InChI=1/C10H14O5/c1-3-9(11)14-7-5-13-6-8-15-10(12)4-2/h3-4H,1-2,5-8H2

Upstream product

• 292638-85-8 acrylic acid methyl ester 
• 111-46-6 diethylene glycol 
• 75-21-8 oxirane 
• 79-10-7 acrylic acid 
• 814-68-6 acryloyl chloride 

Downstream Products

• 875916-85-1 acrylic acid 2-[2-(2-chloro-3-p-tolyl-propionyloxy)-ethoxy]-ethyl ester 
• 447403-75-0 acrylic acid 2-[2-(2-thiocyanato-3-p-tolyl-propionyloxy)-ethoxy]-ethyl ester 
• 447403-72-7 1-acryloyloxy-2-[2-(2-thiocyanato-3-phenylpropionyloxy)ethoxy]ethane 
• 81165-45-9 3-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-propionic acid 2-(2-{3-[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-propionyloxy}-ethoxy)-ethyl ester; compound with oxalic acid 

Relevant articles and documents

Method for catalytically synthesizing diethylene glycol di(methyl) acrylate by calcium glyceroxide

The invention discloses a method for catalytically synthesizing diethylene glycol di(methyl) acrylate by calcium glyceroxide, and belongs to the field of fine chemical engineering. (Methyl) alkyl acrylate and diethylene glycol are used as raw materials; a reaction-rectification coupling process is adopted; a copper-wire-net-filled modified rectification column is used; the catalyst calcium glyceroxide is added; enough product purity and yield can be obtained after a simple aftertreatment process. The method overcomes multiple disadvantages of an existing transesterification catalyst, and is high in yield and simple in post-processing. Compared with a conventional transesterification method, the method provided by the invention can improve the total yield and the processing capacity; energy needed for separation is supplied by utilizing reaction heat, so that the energy consumption is decreased, and an investment is reduced. The method provided by the invention is simple and short in process flow; the raw materials are easily obtained; equipment is simple; reaction conditions are easy to control. The method is mild in the reaction conditions and simple in purification and refining processes; a product is stable, is easy to separate, and is not liable to generate a polymerization phenomenon.

COMPOSITION FOR POLYELECTROLYTES, POLYELECTROLYTES, ELECTRICAL DOUBLE LAYER CAPACITORS AND NONAQUEOUS ELECTROLYTE SECONDARY CELLS

A polymer electrolyte-forming composition containing (A) a quaternary ammonium salt of general formula (1) below and (B) an ionic liquid can be converted into a polymer without compromising the excellent properties of the ionic liquid, thus enabling an electrolyte having an excellent safety and electrical conductivity and also a broad potential window to be obtained. In formula (1), R1 to R3 are each independently an alkyl group of 1 to 5 carbons or a substituent having a reactive unsaturated bond and any two from among R1 to R3 may together form a ring, and R4 is methyl, ethyl or a substituent having a reactive unsaturated bond, with the proviso that at least one of R1 to R4 is a substituent having a reactive unsaturated bond. X is a monovalent anion, the letter m is an integer from 1 to 8, and the letter n is an integer from 1 to 4.

Process for the alkoxylation of organic compounds in the presence of novel framework materials

The present invention relates to a process for the alkoxylation of organic compounds comprising the reaction of at least one organic compound with at least onealkoxylating agent in the presence of a catalyst system, wherein a polyetheralcohol is obtained. The catalyst system comprises a metallo organic framework mate-rial comprising pores and at least one metal ion and at least one at least bidentate organic compound, which is coordinately bounded to said metal ion. Furthermore it relates to polyurethanes or polyurethane foams, which are obtainable by using a prepared polyether alcohol as a starting material.