Tertiary alcohols
Tertiary alcohols are a class of organic compounds characterized by having three carbon atoms attached to the alcohol functional group (-OH) with no hydrogen atoms directly bonded to the oxygen atom. These molecules play significant roles in various industrial applications, including solvents, pharmaceuticals, and cosmetics. Their unique structure imparts properties such as low reactivity towards many common chemical reactions, making them useful as intermediates or stabilizers. Due to their stability, tertiary alcohols are often employed in scenarios requiring the protection of functional groups or minimizing unwanted side reactions during synthetic processes. In pharmaceutical development, certain tertiary alcohols can serve as solubilizing agents or protectants for drug molecules. Additionally, they find applications in personal care products where they contribute to improved texture and stability. The versatile nature of these compounds makes them indispensable in a wide range of chemical industries.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1-hydroxycyclobutane-1-carbonitrile | 55767-58-3 | C5H7NO |
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(2R)-2-Oxiranyl-6-methyl-5-heptene-2-ol | 76985-29-0 | C10H18O2 |
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2-Propanol,1,1,1-tribromo-2-methyl- | 76-08-4 | C4H7Br3O |
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4,4-dimethoxy-2-methylbutan-2-ol | 31525-67-4 | C7H16O3 |
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1-Hexen-3-ol,3,5-dimethyl- | 3329-48-4 | C8H16O |
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4-(1S)-1-amino-2-methylpropylhepta-1,6-dien-4-ol | 315248-94-3 | C11H21NO |
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Grayanotox-10(20)-ene-3,5,6,14,16-pentol,14-acetate, (3b,6b,14R)- | 30272-17-4 | C22H34O6 |
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2,4-Cyclohexadiene-1-acetonitrile,3,5-dibromo-1,6-dihydroxy-4-methoxy-, (1R,6S)- | 30951-40-7 | C9H9Br2NO3 |
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1-Penten-3-ol,4,4,5,5,5-pentafluoro-3-methyl- | 754-67-6 | C6H7F5O |
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4-Methyl-5,5,5-trifluoropent-1-en-4-ol | 73893-33-1 | C6H9F3O |
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