1663-39-4 Usage
Description
t-Butyl acrylate, also known as tert-butyl acrylate, is a clear liquid monomer with the chemical formula C7H12O2. It is an essential component in the production of various polymers and has a wide range of applications across different industries due to its unique chemical properties.
Uses
Used in Polymer Production:
t-Butyl acrylate is used as a monomer for the synthesis of poly(tert-butyl acrylate) (PtBA) polymers and copolymers. These polymers are known for their excellent properties, such as high molecular weight, thermal stability, and resistance to degradation, making them suitable for various applications.
Used in Paints and Coatings Industry:
t-Butyl acrylate is used as a component in the formulation of paints and coatings. Its incorporation into these products enhances their durability, adhesion, and resistance to environmental factors, such as UV radiation and moisture.
Used in High Polymer Paper Conditioner:
In the paper industry, t-Butyl acrylate is used as a high polymer paper conditioner. It improves the paper's strength, smoothness, and resistance to tearing, making it more suitable for various printing and packaging applications.
Used in Nursing Polymer Products:
t-Butyl acrylate is also utilized in the production of nursing polymer products, such as diapers and incontinence pads. Its presence in these products contributes to their absorbency, comfort, and overall performance.
Used in Carbonyl Reforming Polyolefin:
t-Butyl acrylate serves as an important raw material in the carbonyl reforming of polyolefins. This process involves the conversion of olefins, such as ethylene and propylene, into valuable chemicals and materials, which find applications in various industries.
Used in Organic Synthesis:
t-Butyl acrylate is an essential raw material in organic synthesis, where it is used to produce various chemicals and compounds with diverse applications, such as pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Radiation Polymerization:
t-Butyl acrylate undergoes radiation polymerization to form TBA-gels, which are used in radio-fluorogenic dose imaging applications. These gels provide a means to visualize and measure the distribution of radiation doses in various materials, which is crucial in medical and industrial settings.
Used as a Reactive Diluent:
In some studies, t-Butyl acrylate may be used as a reactive diluent. Its presence in the formulation can improve the processability and performance of the final product, making it a valuable addition to the formulation.
Flammability and Explosibility
Flammable
Check Digit Verification of cas no
The CAS Registry Mumber 1663-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1663-39:
(6*1)+(5*6)+(4*6)+(3*3)+(2*3)+(1*9)=84
84 % 10 = 4
So 1663-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-5-6(8)9-7(2,3)4/h5H,1H2,2-4H3
1663-39-4Relevant articles and documents
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Castro,Rust
, p. 4928,4931 (1961)
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Activated Self-Resolution and Error-Correction in Catalytic Reaction Networks**
Schaufelberger, Fredrik,Ramstr?m, Olof
supporting information, p. 10335 - 10340 (2021/05/07)
Understanding the emergence of function in complex reaction networks is a primary goal of systems chemistry and origin-of-life studies. Especially challenging is to create systems that simultaneously exhibit several emergent functions that can be independently tuned. In this work, a multifunctional complex reaction network of nucleophilic small molecule catalysts for the Morita-Baylis-Hillman (MBH) reaction is demonstrated. The dynamic system exhibited triggered self-resolution, preferentially amplifying a specific catalyst/product set out of a many potential alternatives. By utilizing selective reversibility of the products of the reaction set, systemic thermodynamically driven error-correction could also be introduced. To achieve this, a dynamic covalent MBH reaction based on adducts with internal H-transfer capabilities was developed. By careful tuning of the substituents, rate accelerations of retro-MBH reactions of up to four orders of magnitude could be obtained. This study thus demonstrates how efficient self-sorting of catalytic systems can be achieved through an interplay of several complex emergent functionalities.
Palladium-catalyzed regioselective synthesis of B(4,5)-or B(4)-substituted: O-carboranes containing α,β-unsaturated carbonyls
Li, Jiaoyi,Lu, Jian,Tian, Song,Wang, Qian,Zhang, Chuyi,Zhang, Jianwei,Zhou, Ling
supporting information, p. 4723 - 4727 (2020/07/13)
With the help of a carboxylic acid directing group, Pd-catalyzed regioselective synthesis of B(4,5)-or B(4)-substituted o-carboranes containing α,β-unsaturated carbonyls has been reported. The-COOH, removed during the course of the reaction, is responsible for controlling the regioselectivity. The desired products could be obtained in moderate to good yields.