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Home > Organic Chemistry > Alcohols, Phenols, Phenol Alcohols (Find 45 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-Naphthol

(135-19-3)
2-Naphthol, a compound of great importance in the field of chemistry, is the product of a series of metabolic processes in living organisms, mainly catalyzed by isozymes of the cytochrome P450 family, such as CYP 1A1, CYP 1A2, CYP 2A1, CYP 2E1, and CYP 2F2. This compound exists in the form of dry powder or liquid/solid, with a crystalline appearance ranging from white to pale yellow, emitting a unique odor, which is a distinctive chemical characteristic. The structural feature of 2-naphthol lies in its naphthol structure with a hydroxyl group at the 2nd position, which endows it with a series of biological activities. It is recognized as an antinematode agent, exerting inhibitory effects on nematodes, while its chemical properties also make it considered a genetically toxic substance, potentially affecting genetic material. Furthermore, 2-naphthol is an exogenous metabolite of humans and mice, commonly found in human urine, showing its metabolic pathway in the body. It also possesses the characteristic of a free radical scavenger, possibly participating in the body's antioxidant mechanism. In terms of physical and chemical properties, the density of 2-naphthol is 1.28 g/cm³ at 20°C, its melting point is 121.6°C, and its boiling point is 285°C, with a certain degree of volatility. Its flash point is 160°C, indicating the risk of fire or explosion in high-temperature environments. Its refractive index is 1.548, and its water solubility is extremely low, only able to dissolve in water at extremely low concentrations (1 g/L, 20°C). These characteristics are crucial for safe handling in laboratories and industrial production. When storing and handling 2-naphthol, strict adherence to safety regulations must be followed. It should be stored away from heat sources, sparks, and flames, and should be avoided in contact with open flames. At the same time, it should be stored away from direct sunlight to prevent it from degrading due to photochemical reactions. Keeping the container closed can prevent evaporation and reaction with oxygen in the air. The vapor pressure of 2-naphthol is 10 mm Hg (145.5°C) and its vapor density is 4.97 (relative to air), indicating that it may form flammable vapors under certain conditions. It has a weak phenolic odor and may irritate the respiratory system. Additionally, its hydroxyl radical reaction rate constant and autoignition temperature, among other parameters, reveal the chemical reactions it may participate in under certain conditions, suggesting that extra care is needed when handling and using it. In experimental operations, appropriate personal protective equipment such as chemical protective goggles, respiratory protection devices, and chemical protective gloves should be used to prevent skin contact and inhalation of its vapors. If accidental inhalation occurs, personnel should be immediately moved to fresh air and seek medical assistance. After skin contact, immediate rinsing with plenty of water should be done and medical attention sought promptly. Additionally, 2-naphthol may also contaminate the environment, so any spills or waste should be disposed of according to local regulations and not discarded carelessly. In analysis and synthesis work, special sealed equipment is typically used for operation to reduce exposure and prevent leaks. In cases where heating is required, a water bath or oil bath should be used, avoiding direct flame heating to reduce the risk of fire or explosion. At the same time, its solutions should be stored in a dark place to slow down its possible photochemical reactions. The solubility of 2-naphthol is higher in organic solvents such as alcohol, ketone, and ether, which makes it have certain application value in organic synthesis. However, these characteristics also increase the risk of forming a mixture of solvent vapors during handling, so it should be carried out in a well-ventilated environment and with good ventilation facilities. Understanding these properties of 2-naphthol is crucial in research and industrial production, not only for the safety of experimental personnel but also for the quality of products and environmental protection. Therefore, it is necessary to have a thorough understanding of the properties of 2-naphthol and strictly follow safety operating procedures before conducting related work.

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2-Ethylhexanol

(104-76-7)
GB2760-1996 allows the use of edible spices. Used in the production of plasticizers, defoamers, dispersants, mineral processing agents and petroleum additives, also used in printing and dyeing, paints, films, etc.; used in the production of plasticizers, defoamers, dispersants, mineral processing agents and petroleum additives It is also used in printing and dyeing, paint, film, etc.; 2-ethylhexanol is customarily called octanol in the plasticizer neighborhood, and it is an important chemical ra

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2,2-Bis(4-hydroxyphenyl)propane

(80-05-7)
It is an important raw material for the synthesis of polycarbonate, epoxy resin, and high-temperature resistant polyester. It is also used as a PVC stabilizer, plastic antioxidant, ultraviolet absorber, bactericide, etc.; Bisphenol A is a product with a wide range of uses. Used to produce epoxy resin, polycarbonate, polyester resin, polyphenylene ether resin, polysulfone resin. It can also be used as polyvinyl chloride stabilizer, plastic antioxidant, ultraviolet absorber, agricultural bacterici

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2-Octanol

(123-96-6)
Solvents, defoamers, perfume intermediates, plasticizer preparation, organic synthesis, petroleum additives, wetting agents.

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2-Chlorophenol

(95-57-8)
Used in medicine, pesticides and dyes and other organic synthetic materials

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2,3-Butanediol

(513-85-9)
Used for preparing resin and used as solvent, etc.

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2,6-Di-tert-butylphenol

(128-39-2)
Antioxidant for Gasoline, Jet Fuels, and Electrical Insulating Oils Antioxidant Intermediate, Pharmaceuticals

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2-(Methylamino)ethanol

(109-83-1)
N-Methylethanolamine is an alkanolamine and a toxic, flammable, corrosive, colorless, viscous liquid. It is the biochemical precursor of choline.With both an amine and an hydroxyl functional groups, it is a useful intermediate in the chemical synthesis of various products including polymers and pharmaceuticals. It is also used as a solvent, for example in the natural gas-processing industry together with its analogs ethanolamine and dimethylethanolamine.N-Methylethanolamine can be prepared by th

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2,3-Dibromo-1-propanol

(96-13-9)
2,3-Dibromo-1-propanol is a metabolite of the flame retardant tris(2,3-dibromopropyl) phosphate (T775560), previously shown to be a mutagen and carcinogen in experimental animals.

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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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