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Home > Organic Chemistry > Alcohols, Phenols, Phenol Alcohols (Find 305 items)
Discover the versatile applications of isopropyl alcohol (IPA) and its role in various industries. Explore the realm of phenolic compounds, including phenolic resin and other phenolic materials. Learn about phenolic acids and phenol uses. Uncover the CAS NO., properties, and SDS of each compound. Acquire raw alcohol, phenol, and phenol alcohol materials from reputable suppliers, ensuring detailed product information.

(+)-2,3-Butanediol

(19132-06-0)
SLIGHTLY YELLOW OILY LIQUIDChEBI: The (S,S) diastereoisomer of butane-2,3-diol.2, 3-Butanediol, which is very important for a variety of chemical feedstocks and liquid fuels, can be derived from the bioconversion of natural resources1-2. It may be used in the production of antifreeze solvents, extraction solvents, butadiene, polymers, polyurethane and diacetyl and may also be used as a fuel1, 2.

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Tetrahydrofurfuryl alcohol

(97-99-4)
Solvent for fats, waxes, resins, in organic synthesis.

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4-Methyl-2-pentanol

(108-11-2)
4-Methyl-2-pentanol is an excellent medium boiling point solvent. Mainly used as a solvent for dyes, petroleum, rubber, resins, paraffin, nitrocellulose and ethyl cellulose, and as an inert solvent for nitrocellulose paint, which can increase the gloss and flatness of the coating and improve the redness performance; Used as a solvent in the manufacture of lubricant additives. Raw material for organic synthesis, mineral flotation lotion, such as extraction of silicon and copper sulfate ore; can a

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Triisopropanolamine

(122-20-3)
Triisopropanolamine is used as an emulsifying agent. Emulsifying agents.

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[1,1′-Biphenyl]-2-ol

(90-43-7)
2-phenylphenol is remarkably versatile organic chemical products, widely used antiseptic, auxiliaries and surfactant synthesis of new plastics, resins and polymer materials in areas such as stabilizers and flame retardants.

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tert-Butyl hydroperoxide

(75-91-2)
Catalyst in polymerization reactions.To introduce peroxy group into org molecules, in radical substitution reactions:Kharasch, Fono, J. organic. Chem. 23, 325 (1948); see also Kharasch, Sosnovsky, Tetrahedron 3, 97, 105 (1958).

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1-Heptanol

(111-70-6)
1-Heptanol have also been used in the fragrance industry due to its pleasant smell.

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α-Terpineol

(98-55-5)
Shows antioxidant effects. Antiseptic. is present in many extracted oils of various plant species, acts as an antihypernociception and anti-inflammatory.

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Alcohols are a large class of organic compounds. They are compounds in which the hydrogen atoms in the side chains of aliphatic hydrocarbons, alicyclic hydrocarbons, or aromatic hydrocarbons are replaced by hydroxyl groups. The hydroxyl group is connected to the benzene ring, and it is classified as phenol because of its chemical properties that are different from ordinary alcohols. Phenol is an important chemical raw material and can be used to manufacture dyes, drugs, phenolic resins, adhesives, etc. There are many types of phenolic compounds, including phenol, cresol, aminophenol, nitrophenol, naphthol, chlorophenol and so on. "Alcohols, Phenols, Phenol Alcohols" on ECHEMI mainly includes: cyclitols, Alcohol derivatives, Phenol Alcohols derivatives, Phenol derivatives, Acyclic alcohols.

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Alcohols, phenols, and phenol alcohols are pivotal chemical compounds employed in diverse industrial applications, ranging from pharmaceuticals to personal care products. Alcohols, characterized by the presence of a hydroxyl (-OH) group, are widely utilized as solvents, disinfectants, and antiseptics. Ethanol, for instance, is commonly used in hand sanitizers and disinfectants due to its antimicrobial properties. Phenols, featuring a hydroxyl group attached to an aromatic ring, exhibit strong antiseptic and disinfectant properties. Phenol alcohols, compounds that combine features of both alcohols and phenols, offer a unique blend of properties. One example is benzyl alcohol, which serves as a solvent, preservative, and fragrance ingredient in cosmetic formulations.

The synthesis of alcohols, phenols, and phenol alcohols involves a range of chemical reactions, including hydroxylation, oxidation, and esterification. By carefully controlling these reactions, chemists can tailor the properties of these compounds to meet specific application requirements, ensuring their effectiveness and safety in various industrial and consumer products.

Common phenol uses:
● Disinfectants and antiseptics
● Chemical intermediates
● Adhesives and resins
● Textile manufacturing
● Herbicides
● Personal care products

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