Pentan-2-ol
Pentan-2-ol, also known as sec-amyl alcohol, is an organic compound with the chemical formula C₅H₁₂O. It is one of the isomers of pentanol, a type of alcohol with five carbon atoms. Pentan-2-ol is a secondary alcohol, meaning the hydroxyl group (-OH) is attached to a secondary carbon atom, which is a carbon atom bonded to two other carbon atoms.
Structure and Properties[edit | edit source]
Pentan-2-ol has the following structural formula:
CH₃-CH(OH)-CH₂-CH₂-CH₃
This structure indicates that the hydroxyl group is attached to the second carbon in the pentane chain. As a secondary alcohol, pentan-2-ol can undergo oxidation to form a ketone, specifically pentan-2-one.
Physical Properties[edit | edit source]
- Molecular Weight: 88.15 g/mol - Density: 0.81 g/cm³ - Boiling Point: 119 °C (246 °F) - Melting Point: -60 °C (-76 °F) - Solubility: Moderately soluble in water; miscible with most organic solvents.
Chemical Properties[edit | edit source]
Pentan-2-ol is a flammable liquid and should be handled with care. It can participate in typical alcohol reactions, such as: - Oxidation: Can be oxidized to pentan-2-one using oxidizing agents like potassium dichromate or chromic acid. - Esterification: Reacts with carboxylic acids to form esters in the presence of an acid catalyst. - Dehydration: Can undergo dehydration to form alkenes, such as pent-2-ene, in the presence of an acid catalyst.
Synthesis[edit | edit source]
Pentan-2-ol can be synthesized through the hydration of pentenes, specifically 2-pentene, using an acid catalyst. This process involves the addition of water across the double bond of the alkene.
Applications[edit | edit source]
Pentan-2-ol is used in the synthesis of various chemical compounds and as a solvent in the laboratory. It is also used in the production of perfumes and flavorings due to its pleasant odor.
Safety and Handling[edit | edit source]
Pentan-2-ol is a flammable liquid and should be stored in a cool, well-ventilated area away from sources of ignition. It can cause irritation to the skin and eyes, and inhalation of vapors may cause respiratory irritation. Proper personal protective equipment, such as gloves and goggles, should be used when handling this chemical.
Also see[edit | edit source]
- Pentanol - Alcohol (chemistry) - Secondary alcohol - Pentan-2-one - Esterification
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