1、Vinyl Acetate
Vinyl acetate is an industrial chemical that is produced in large amounts in the United States. It is a clear, colorless liquid with a sweet, fruity smell. It is very flammable and may be ignited by heat, sparks, or flames. Vinyl acetate is used to make other industrial chemicals.
2、Vinyl Acetate: A Deep Dive into its Structural Formula and Molecular
This guide provides an in-depth analysis of its structural formula and three-dimensional geometry, supported by quantitative data from spectroscopic studies. The molecule consists of a planar vinyl group attached to an acetate group, with key bond lengths and angles determined with high precision.
3、Vinyl acetate
Vinyl acetate (CAS 108-05-4) information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices, suppliers, SDS and more, available at Chemicalbook.
4、Acetic acid ethenyl ester
Acetic acid ethenyl ester Formula: C 4 H 6 O 2 Molecular weight: 86.0892 IUPAC Standard InChI: InChI=1S/C4H6O2/c1-3-6-4 (2)5/h3H,1H2,2H3 Copy
Vinyl acetate
ChemSpider record containing structure, synonyms, properties, vendors and database links for Vinyl acetate, 108-05-4, VAC, XTXRWKRVRITETP-UHFFFAOYSA-N
PubChemLite
Structural Information Molecular Formula C4H6O2 SMILES CC (=O)OC=C InChI InChI=1S/C4H6O2/c1-3-6-4 (2)5/h3H,1H2,2H3 InChIKey XTXRWKRVRITETP-UHFFFAOYSA-N Compound name ethenyl acetate Related CIDs CID 7904 CID 16213619
Structural Formula of Vinyl Acetate Monomer
The structural formula of vinyl acetate is CH3COO-CH=CH2, representing an unsaturated carboxylic acid ester and a vinyl ester compound. Properties of Vinyl Acetate
vinyl acetate (CH3COOCHCH2) 3D molecular structure
Examples of 3D molecular structures: H2O, CO2, CH4, NH3, HCl, H2S, SO2, SO3, C2H4, C2H6, C6H6, caffeine, melatonin, fructose. Interactive 3D molecular viewer displays chemical compounds as rotatable 3D models showing molecular geometry and atomic arrangements. What is 3D molecular visualization?
Vinyl Acetate
Vinyl Acetate (CAS 108-05-4). Properties, structure, safety data, and identifiers.
Vinyl Acetate
Use: In polymerized form for plastic masses, films and lacquers; in plastic film for food packaging. As modifier for food starch.
In the vast realm of chemistry, every compound carries its unique story and mysteries. Vinyl acetate, a name that seems simple, conceals a complex world of organic chemistry. It is not merely a substance but a bridge connecting nature to human technology. Its structural formula, like a window, allows us to glimpse the intricate molecular architecture within.
The structure of vinyl acetate consists of a carbon atom, an oxygen atom, and a hydrogen atom connected by a double bond. This seemingly straightforward arrangement contains profound information. The most striking feature is the double bond, a key determinant of vinyl acetate's properties. The presence of this double bond endows vinyl acetate with paramagnetism, enabling it to be attracted to magnets.
Paramagnetism refers to a material's tendency to align with an external magnetic field, a property often linked to unpaired electrons in molecules. In vinyl acetate, the unpaired electrons in the double bond share space between two atomic nuclei, giving the molecule its paramagnetic character.
Beyond the double bond, vinyl acetate's structure includes a carboxyl group (-COOH). This polar functional group dictates the compound's acidity and reactivity. The oxygen atom in the carboxyl group bears a negative charge, while the attached hydrogen atom carries a positive charge. This uneven distribution of charges gives vinyl acetate its acidic properties. Additionally, the carboxyl group enables vinyl acetate to participate in chemical reactions, playing roles in various biological processes.
Scientists have extensively studied both the physical and chemical properties of vinyl acetate. Through experiments and theoretical calculations, they have revealed its stability and reactivity under different conditions. For instance, when heated or exposed to light, vinyl acetate may decompose or polymerize, releasing new substances. These reactions not only illuminate its chemical essence but also open avenues for synthesizing novel organic compounds.
Vinyl acetate has broad applications. It serves as a critical precursor in materials synthesis and plays significant roles in pharmaceuticals and agriculture. By reacting vinyl acetate with other chemicals, scientists can produce diverse polymers and drugs, enriching human health and life.
Researchers continue to uncover new phenomena and patterns in vinyl acetate. They have found that changes in temperature and pressure can alter its structure, offering fresh perspectives on molecular interactions. its solubility and reactivity vary in different solvents, guiding the selection of optimal conditions for reactions.
Interestingly, vinyl acetate's paramagnetism correlates with its concentration and temperature. Higher concentration or temperature amplifies its paramagnetic response, while lower values diminish it. This discovery provides new insights into studying material magnetism.
Beyond magnetism, vinyl acetate exhibits other fascinating traits. Under ultraviolet light, it fluoresces, making it a valuable tool for detecting specific molecules in biological samples. Its biocompatibility also ensures safe use in biomedical fields.
studying vinyl acetate poses challenges. Researchers must navigate extreme experimental conditions, such as high temperatures and pressures, and complex procedures. Ensuring accuracy and reliability of data remains a priority.
Despite these hurdles, scientists persist in exploring vinyl acetate's potential. They believe that deeper understanding of its structural formula will unlock new benefits for society.
As a common organic compound, vinyl acetate's structural formula offers a gateway into chemistry. By studying it, we gain insights into its properties and reactivity, advancing scientific research and applications. More importantly, it inspires further exploration in the chemical frontier.
