3-[2,2-Dimethyl-3-(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate
[CAS# 84170-74-1]

Identification

• Classification: Catalysts and additives >> Polymer
• Name: 3-[2,2-Dimethyl-3-(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate
• Molecular Formula: C₁₇H₂₈O₆
• Molecular Weight: 328.40
• CAS Registry Number: 84170-74-1
• EC Number: 617-546-6
• SMILES: CC(C)(COCCCOC(=O)C=C)COCCCOC(=O)C=C

Properties

• Density: 1.0±0.1 g/cm³, Calc.^*, 1.1007 g/cm³, (25 ºC)
• Index of Refraction: 1.459, Calc.^*
• Boiling Point: 407.9±40.0 ºC (760 mmHg), Calc.^*
• Flash Point: 175.0±27.4 ºC, Calc.^*, 113 ºC

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07;GHS09 Warning
• Hazard Statements: H315-H317-H319-H335-H411
• Precautionary Statements: P261-P264-P264+P265-P271-P272-P273-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P333+P313-P337+P317-P362+P364-P391-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Chronic hazardous to the aquatic environment	Aquatic Chronic	2	H411
Skin sensitization	Skin Sens.	1B	H317
Eye irritation	Eye Irrit.	2	H319
Skin irritation	Skin Irrit.	2	H315
Skin sensitization	Skin Sens.	1	H317
Specific target organ toxicity - single exposure	STOT SE	3	H335

Discovory and Applicatios

3-[2,2-Dimethyl-3-(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate is a specialized chemical compound used primarily in polymer chemistry and materials science. Its discovery emerged from the search for new monomers that could offer enhanced properties in polymer systems, leading to its integration into various industrial applications.

The compound is characterized by its complex structure, which includes multiple functional groups such as the prop-2-enoate ester and ether linkages. These features contribute to its unique reactivity and compatibility with other monomers. The development and introduction of this compound were driven by the need for more versatile monomers that could produce polymers with tailored properties for specific applications.

In practical applications, 3-[2,2-Dimethyl-3-(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate is used in the formulation of specialty polymers and copolymers. Its ability to participate in polymerization reactions and form stable, high-performance polymers makes it valuable in a variety of fields. For instance, polymers derived from this compound are often used in coatings, adhesives, and sealants where enhanced durability and resistance to environmental factors are required.

The presence of the dimethyl and propoxy groups in the compound contributes to the improved mechanical and chemical properties of the resulting polymers. This makes them suitable for applications that demand high-performance materials with resistance to heat, chemicals, and physical stress. Additionally, the compound's ability to cross-link with other monomers enhances the structural integrity and longevity of the polymers.

Another notable application of this compound is in the production of functional materials. The unique combination of functional groups in its structure allows for the creation of polymers with specific attributes, such as improved flexibility or rigidity, depending on the intended use. This versatility is highly valued in industries that require custom-tailored materials for advanced applications.

In summary, 3-[2,2-Dimethyl-3-(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate is an important monomer in polymer chemistry. Its unique chemical structure and properties make it a valuable component in the development of high-performance polymers for a range of industrial applications.