Methyl pivalate
Methyl pivalate, also known as methyl trimethylacetate, is an organic compound with the chemical formula C_6H_12O_2. It is a methyl ester of pivalic acid (trimethylacetic acid) and is used in various chemical syntheses and industrial applications. This compound is part of the larger family of carboxylic acid esters, which are important in both natural processes and industrial applications.
Properties[edit | edit source]
Methyl pivalate is a colorless, flammable liquid with a characteristic ester odor. It is soluble in organic solvents such as ethanol, diethyl ether, and benzene, but has limited solubility in water. The compound has a boiling point of approximately 102°C and a melting point of -48.5°C. Its molecular weight is 116.16 g/mol.
Synthesis[edit | edit source]
Methyl pivalate is typically synthesized through the esterification of pivalic acid with methanol. This reaction is often catalyzed by an acid, such as sulfuric acid, to facilitate the conversion. The process involves heating the reactants and continuously removing the water formed during the reaction to drive the equilibrium towards the formation of the ester.
Applications[edit | edit source]
Methyl pivalate is used in a variety of chemical syntheses and industrial applications. It serves as a starting material in the synthesis of other organic compounds, including plasticizers, synthetic lubricants, and pharmaceuticals. Additionally, it is used as a solvent and as an intermediate in the manufacture of pesticides and perfumes. Its volatility and solubility properties make it a valuable compound in the formulation of paints and coatings.
Safety[edit | edit source]
As with many organic solvents, methyl pivalate poses certain health and safety risks. It is flammable and should be handled with care to avoid fire hazards. Inhalation or ingestion of methyl pivalate can cause irritation to the respiratory tract and digestive system. Proper protective equipment, such as gloves and goggles, should be worn when handling this chemical to prevent skin and eye contact.
Environmental Impact[edit | edit source]
The environmental impact of methyl pivalate depends on its concentration and the context of its release. As an organic compound, it has the potential to contribute to Volatile Organic Compounds (VOCs) in the atmosphere, which are precursors to ozone formation and can affect air quality. Proper disposal and handling procedures should be followed to minimize its release into the environment.
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD