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Carbitol acrylate
[CAS# 7328-17-8]

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Identification
ClassificationOrganic raw materials >> Carboxylic compounds and derivatives >> Carboxylic esters and their derivatives
NameCarbitol acrylate
SynonymsEthoxyethoxyethyl acrylate; 2-(2-Ethoxyethoxy)ethyl acrylate; Di(ethylene glycol) ethyl ether acrylate
Molecular StructureCAS # 7328-17-8, Carbitol acrylate
Molecular FormulaC9H16O4
Molecular Weight188.22
CAS Registry Number7328-17-8
EC Number230-811-7
SMILESCCOCCOCCOC(=O)C=C
Properties
Density1.016
Boiling point95 °C (5 mmHg)
Refractive index1.439
Flash point>110 °C
Safety Data
Hazard Symbolssymbol symbol symbol symbol   GHS05;GHS06;GHS07;GHS09 Danger  Details
Risk StatementsH302-H311-H312-H314-H315-H317-H318-H319-H335-H411-H412  Details
Safety StatementsP260-P261-P262-P264-P264+P265-P270-P271-P272-P273-P280-P301+P317-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P351+P338-P305+P354+P338-P316-P317-P319-P321-P330-P332+P317-P333+P317-P337+P317-P361+P364-P362+P364-P363-P391-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H312
Skin sensitizationSkin Sens.1AH317
Skin sensitizationSkin Sens.1H317
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Specific target organ toxicity - single exposureSTOT SE3H335
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Acute toxicityAcute Tox.3H311
Skin corrosionSkin Corr.1BH314
Skin corrosionSkin Corr.1CH314
SDSAvailable
up Discovery and Applications
Carbitol acrylate, also known as 2-(2-ethoxyethoxy)ethyl acrylate, is a significant compound in the realm of polymer chemistry and materials science. This ester derivative of acrylate is characterized by its ether linkage and acrylate functionality, which imparts unique properties to the polymer systems in which it is used.

The discovery of carbitol acrylate emerged from the need for more versatile and effective acrylate monomers that could improve the performance of various polymer systems. Its chemical structure combines the reactive acrylate group with an ether moiety, resulting in a compound that exhibits favorable polymerization characteristics and compatibility with different types of resins and coatings. The ether linkage provides enhanced solubility and flexibility, while the acrylate group allows for efficient polymerization through free-radical mechanisms.

In practical applications, carbitol acrylate is primarily utilized in the formulation of coatings, adhesives, and sealants. Its incorporation into these products enhances their performance by improving their adhesion, flexibility, and durability. For coatings, carbitol acrylate contributes to the development of films that are resistant to abrasion, chemicals, and environmental conditions. This makes it particularly valuable in industrial and automotive coatings, where long-lasting protection and resilience are essential.

The use of carbitol acrylate in adhesives offers similar benefits, including strong bonding properties and resistance to various stressors. Its ability to form flexible and durable bonds makes it suitable for a wide range of applications, from construction to electronics. Additionally, in sealants, carbitol acrylate helps to create flexible, durable seals that can withstand exposure to moisture, temperature fluctuations, and mechanical stress.

Carbitol acrylate also finds applications in the field of adhesives and sealants, where its low viscosity and excellent wetting properties enhance the performance of various formulations. It is used in the production of pressure-sensitive adhesives and specialty sealants, where its properties contribute to the overall effectiveness and longevity of the final products.

Ongoing research aims to explore further applications of carbitol acrylate and to optimize its properties for new and emerging technologies. Advances in polymer chemistry and material science continue to expand the potential uses of this compound, highlighting its importance in the development of high-performance materials.

References

2021. Streamlined access to end-functionalized thermoresponsive polymers via a combination of bulk RAFT polymerization and quasi solvent-free Passerini three-component reaction. Polymer Journal, 53(12).
DOI: 10.1038/s41428-021-00504-z

2010. Clarification of the Blood Compatibility Mechanism by Controlling the Water Structure at the Blood-Poly(meth)acrylate Interface. Journal of Biomaterials Science, Polymer Edition, 21(8).
DOI: 10.1163/092050610x517220
Market Analysis Reports
List of Reports Available for Carbitol acrylate
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