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Home > Organic Chemistry > Alcohols, Phenols, Phenol Alcohols (Find 9 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.

Isopropanol

(67-63-0)
1. When compared to ethanol, 50% less is required for nucleic acid precipitation, thus minimizing the total volume to be centrifuged for DNA or RNA recovery.
2. Suitable for HPLC, spectrophotometry, environmental testing

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Isobutanol

(78-83-1)
Used as analytical reagent, chromatographic analysis reagent, solvent and extractant; used as a raw material for organic synthesis, and also used as a high-grade solvent; isobutanol is a raw material for organic synthesis and is mainly used as an intermediate for the synthesis of diazinon in pesticides Isobutyronitrile. Organic synthesis raw materials. Used in the manufacture of petroleum additives, antioxidants, 2,6-di-tert-butyl-p-cresol, isobutyl acetate (coating solvent), plasticizers, synth

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Imidazole-1-ethanol

(1615-14-1)

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Isoamyl alcohol

(123-51-3)
Solvent for fats, resins, alkaloids, etc.; manufacture of isoamyl (amyl) Compounds, isovaleric acid, mercury fulminate, pyroxylin, artificial silk, lacquers, smokeless powders; in microscopy; for dehydrating celloidin solutions; for determining fat in milk.

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Isoeugenol

(97-54-1)
A substitute for eugenol. Except for medicine. It can also be used as a raw material for synthetic spices, can also be used to prepare carnation-flavored daily flavors, and can also be used as edible spices.

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Isoeugenol, acetate

(93-29-8)
Because of its stable aroma properties, it is used in soap flavors. Commonly used in the preparation of sweet fragrances for floral flavors and herbal flavors. It is also commonly used as a fixative for carnation and French flavors, and as a matching agent for vanillin. The aroma is similar to clove. But with a rose fragrance and a sweet fragrance like a pod.

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Isophytol

(505-32-8)
preparation of vitamins E and K1.

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Industrial liquors, corn steep liquor

(66071-94-1)

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Iodogen

(51592-06-4)

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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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Other Chemical Drugs Diagnostic Agents Plant Growth Regulators Emulsifier Anthraquinone and Derivatives Standard Phosphorus Compounds Moisturising Agent Deodorant Tonics

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