6701-13-9

Basic information

• Product Name: 1,10-DECAMETHYLENE GLYCOL DIMETHACRYLATE
• Synonyms: 2-Propenoicacid,2-methyl-,1,10-decanediylester;1,10-DECANEDIOL DIMETHACRYLATE;1,10-DECAMETHYLENE GLYCOL DIMETHACRYLATE;1,10-decanediyl bismethacrylate;Bis(methacrylic acid)1,10-decanediyl ester;Bis(methacrylic acid)decane-1,10-diyl ester;Bismethacrylic acid 1,10-decanediyl ester;Bismethacrylic acid decane-1,10-diyl ester
• CAS NO: 6701-13-9
• Molecular Formula: C18H30O4
• Molecular Weight: 310.43
• EINECS: 229-745-1
• Product Categories: monomer
• Mol File: 6701-13-9.mol
• Article Data: 11

Chemical Properties

• Melting Point: 170℃/2mm
• Boiling Point: 386.9°Cat760mmHg
• Flash Point: 181°C
• Appearance: /
• Density: 0.962
• Vapor Pressure: 3.43E-06mmHg at 25°C
• Refractive Index: n/D1.462
• Storage Temp.: 2-8°C
• Water Solubility: 138.6μg/L at 20.3℃
• CAS DataBase Reference: 1,10-DECAMETHYLENE GLYCOL DIMETHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-DECAMETHYLENE GLYCOL DIMETHACRYLATE(6701-13-9)
• EPA Substance Registry System: 1,10-DECAMETHYLENE GLYCOL DIMETHACRYLATE(6701-13-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-52/53-43
• Safety Statements: 26-36/37/39-61-36/37-28
• WGK Germany: 3
• Hazardous Substances Data: 6701-13-9(Hazardous Substances Data)

Usage

Uses

1,10-decamethylene glycol dimethacrylate is a monomer that can be used to make materials for use in dental applications. It could be used to prepare camphorquinone/amine based adhesive.

InChI:InChI=1/C18H30O4/c1-15(2)17(19)21-13-11-9-7-5-6-8-10-12-14-22-18(20)16(3)4/h1,3,5-14H2,2,4H3

Upstream product

• 112-47-0 1,10-Decanediol 
• 79-41-4 poly(methacrylic acid) 
• 80-62-6 methacrylic acid methyl ester 
• 53463-68-6 1-bromo-10-decanol 
• 64-17-5 ethanol 
• 1078-61-1 dihydrocaffeic acid 
• 2107-70-2 3,4-methoxycinnamic acid 
• 203571-40-8 3-(3,4-bis-benzyloxy-phenyl)-acrylic acid ethyl ester 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 23795-02-0 3-(4-hydroxy-phenyl)-propionic acid ethyl ester 
• 4046-02-0 ethyl 4-hydroxy-3-methoxycinnamate 

Relevant articles and documents

METHOD FOR PRODUCING (METH)ACRYLATE COMPOUND CONTAINING HYDROXYL GROUP AND METHOD FOR PRODUCING (METH)ACRYLATE COMPOUND CONTAINING PHOSPHORIC ACID GROUP

PROBLEM TO BE SOLVED: To provide a method for producing a (meth)acrylate compound containing a hydroxyl group, which, when producing a (meth)acrylate compound containing a hydroxyl group, can suppress formation of by-products. SOLUTION: Provided is a method for producing a (meth)acrylate compound (A) which is a (meth)acrylate compound containing a hydroxyl group, comprising a step of reacting an alcohol compound containing a halogen atom and a (meth)acrylic acid salt to obtain the (meth)acrylate compound (A). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

COLORED COMPOSITION

The present invention is to provide a colored composition having higher heat resistance compared with conventional colored compositions. The present invention further relates to: “a polymer having a monomer unit derived from a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond”, “a monomer which has (i) a cationic rhodamine derivative having, as an counter anion, an anion including an aryl group having an electron-withdrawing substituent and an anion group and (ii) an ethylenically unsaturated bond”, “a colored composition comprising the above-described polymer or the monomer”, and “a colored composition for a color filter comprising the above-described polymer or the monomer”.

Carbon nanotubes supported tyrosinase in the synthesis of lipophilic hydroxytyrosol and dihydrocaffeoyl catechols with antiviral activity against DNA and RNA viruses

Hydroxytyrosol and dihydrocaffeoyl catechols with lipophilic properties have been synthesized in high yield using tyrosinase immobilized on multi-walled carbon nanotubes by the Layer-by-Layer technique. All synthesized catechols were evaluated against a large panel of DNA and RNA viruses, including Poliovirus type 1, Echovirus type 9, Herpes simplex virus type 1 (HSV-1), Herpes simplex virus type 2 (HSV-2), Coxsackievirus type B3 (Cox B3), Adenovirus type 2 and type 5 and Cytomegalovirus (CMV). A significant antiviral activity was observed in the inhibition of HSV-1, HSV-2, Cox B3 and CMV. The mechanism of action of the most active dihydrocaffeoyl derivative was investigated against a model of HSV-1 infection.