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Home > Organic Chemistry > Alcohols, Phenols, Phenol Alcohols (Find 15 items)

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Alcohols, Phenols, Phenol Alcohols
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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.

tert-Butylhydroquinone

(1948-33-0)
Excellent antioxidant performance, stronger than BHT, BHA, PG (propyl gallate) and vitamin E; can effectively inhibit Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Brevibacterium aerogenes and other bacteria and black Aspergillus, Aspergillus versicolor, Aspergillus flavus and other microorganisms grow. The antioxidant function of TBHQ is much better than conventional antioxidants. As far as vegetable oil is concerned, the order of antioxidant capacity is: TBHQ>PG>BHT>BHA. Adding T

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Triethylene glycol

(112-27-6)
In various plastics to increase pliability; in air disinfection.

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Triethanolamine

(102-71-6)
GB2760-96 stipulates that the permitted food processing aids are limited to GMP. Used as a clean liquid for removing carbon dioxide or hydrogen sulfide in gas. The esters formed by triethanolamine and higher fatty acids are widely used as detergents, emulsifiers, humectants and lubricants, and are also used to formulate cosmetic balsams. Triethanolamine is also used as preservative and waterproofing agent, analytical reagent and solvent. Used as an activator in the polymerization of nitrile rubb

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Tetrahydrofurfuryl alcohol

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

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Triisopropanolamine

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

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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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tert-Butanol

(75-65-0)
Used as an organic solvent, and also as a raw material for the preparation of medicines and spices; used as a solvent for molecular weight determination and chromatographic analysis reagent; tert-butanol is the insecticide Bubuzizione, hydrazine, tebufenozide, etc., and the acaricide pyridaben , An important intermediate of the herbicide sec-butaline, sodium tert-butoxide is used as an important sodium alkoxide application in the pesticide industry, mainly used in the cyclization reaction of pyr

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Tris(acetylacetonato)chromium

(21679-31-2)
Used in nmr spectroscopy as a relaxation agent.

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TIPA

(19759-70-7)
A fluorescent trifunctional highly symmetric probe.Shows remarkably high nonlinear optical properties

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Trimethallyl isocyanurate

(6291-95-8)

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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.

More Information

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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