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3,6-DIOXAHEPTYL ACRYLATE is a colorless liquid chemical compound belonging to the acrylates family, characterized by a mild odor. It is primarily utilized as a monomer in the synthesis of polymers and resins, enhancing the flexibility, adhesion, and impact resistance of various coatings, adhesives, and sealants. Additionally, it finds applications in the production of specialty plastics and textiles, contributing to the development of diverse industrial products. However, it is essential to exercise caution when handling 3,6-DIOXAHEPTYL ACRYLATE due to its potential health risks upon inhalation, ingestion, or skin exposure.

7328-18-9

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7328-18-9 Usage

Uses

Used in Coatings Industry:
3,6-DIOXAHEPTYL ACRYLATE is used as a monomer to improve the flexibility, adhesion, and impact resistance of coatings, making them more durable and suitable for various applications.
Used in Adhesives and Sealants Industry:
3,6-DIOXAHEPTYL ACRYLATE is used as a monomer to enhance the bonding strength and durability of adhesives and sealants, ensuring their effectiveness in joining and sealing materials.
Used in Specialty Plastics Manufacturing:
3,6-DIOXAHEPTYL ACRYLATE is used as a monomer in the production of specialty plastics, contributing to the development of materials with improved properties for specific applications.
Used in Textile Industry:
3,6-DIOXAHEPTYL ACRYLATE is used as a monomer in the manufacturing of textiles, providing enhanced flexibility and durability to the fabrics.
Used in Other Industrial Applications:
3,6-DIOXAHEPTYL ACRYLATE is used as a monomer in various industrial applications, including the production of resins and other polymers, to improve their performance characteristics and expand their range of uses.

Check Digit Verification of cas no

The CAS Registry Mumber 7328-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7328-18:
(6*7)+(5*3)+(4*2)+(3*8)+(2*1)+(1*8)=99
99 % 10 = 9
So 7328-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O4/c1-3-8(9)12-7-6-11-5-4-10-2/h3H,1,4-7H2,2H3

7328-18-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyethoxy)ethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names acrylic acid 2-(2-methoxy-ethoxy)-ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7328-18-9 SDS

7328-18-9Downstream Products

7328-18-9Relevant academic research and scientific papers

A supramolecular miktoarm star polymer based on porphyrin metal complexation in water

Hou, Zhanyao,Dehaen, Wim,Lyskawa, Jo?l,Woisel, Patrice,Hoogenboom, Richard

supporting information, p. 8423 - 8426 (2017/08/02)

A novel supramolecular miktoarm star polymer was successfully constructed in water from a pyridine end-decorated polymer (Py-PmDEGA) and a metalloporphyrin based star polymer (ZnTPP-(PEG)4) via metal-ligand coordination. The Py-PmDEGA moiety was prepared via a combination of reversible addition-fragmentation chain transfer polymerization (RAFT) and subsequent aminolysis and Michael addition reactions to introduce the pyridine end-group. The ZnTPP(PEG)4 star-polymer was synthesized by the reaction between tetrakis(p-hydroxyphenyl)porphyrin and toluenesulfonyl-PEG, followed by insertion of a zinc ion into the porphyrin core. The formation of a well-defined supramolecular AB4-type miktoarm star polymer was unambiguously demonstrated via UV-Vis spectroscopic titration, isothermal titration calorimetry (ITC) and diffusion ordered NMR spectroscopy (DOSY).

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