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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.

Xylitol

(87-99-0)
As a food sweetener; it is a special sweetener with nutritional value. It dissolves in water and absorbs heat, has a cool taste when eaten, and does not cause caries. It is also suitable for diabetes. my country stipulates that it can be used in cakes, beverages, and candies to replace cane sugar, and use it in appropriate amounts according to production needs. Nutritional sweetener, mainly for diabetics and as a sweetener for preventing dental caries. moisturizer. Organic synthetic raw material

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1,4-Butanediol

(110-63-4)
Butanediol and its derivatives is used in a broad spectrum of applications in the chemical industry; amongst others in the manufacturing of technical plastics,polyurethanes, solvents, electronic chemicals and elastic fibres. 1,4-Butanediol is used in the synthesis of epothilones, a new class of cancer drugs. Also used in the stereoselective synthesis of (-)-Brevisamide. 1,4-Butanediol's largest use is within tetrahydrofuran (THF) production, used to make polytetramethylene ether glycol, which go

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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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Furfuryl alcohol

(98-00-0)
It is a good solvent and rocket fuel for resins, varnishes and pigments. It can also be used in synthetic fibers, rubber, pesticides and foundry industries. It is also used as a raw material for the synthesis of various furan resins and anticorrosive coatings. It is also a good solvent; GB2761--1997 Specified as permitted food flavors. Mainly used to prepare coke-flavored flavors. FDA, §175.105: It is specified as an indirect food additive (binder). Furfuryl alcohol is used in organic synthesis,

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(-)-β-Sitosterol

(83-46-5)
1. A common sterol in plants. Isolated from wheat germ oil, corn oil. Antilipemic. Used in the treatment of prostatic adenoma.
2. Antiinflammatory, immunomodulator

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(4-Fluoroazepan-4-yl)methanol hydrochloride

(1823319-26-1)

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Ethylene glycol

(107-21-1)
Mainly used in the production of polyester resins, alkyd resins, plasticizers, antifreezes, and also used in cosmetics and explosives; used as analytical reagents, chromatographic analysis reagents and capacitor media; ethylene glycol is the fungicide tebuconazole and moxa The intermediate of the spirit. Gas chromatographic stationary liquid (maximum use temperature 50℃, solvent is chloroform), separation and analysis of low-boiling oxygen-containing compounds, amine compounds, nitrogen or oxyg

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Methanol

(67-56-1)
1. Meets ACS specifications
2. Suitable for HPLC, spectrophotometry, and some LC-MS applications
3. High purity grade for ICP-MS detection
4. Suitable for volatile organics analysis by GC-MS

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1-Propanol

(71-23-8)
Generally used as a solvent, but also as a raw material for preparing n-propylamine, etc. Used as a chromatographic analysis reagent, solvent and cleaning agent; extraction solvent; GB27601996: food flavors, food processing aids. Propanol is used directly as a solvent or in the synthesis of propyl acetate, in coating solvents, printing inks, cosmetics, etc., in the production of n-propylamine as intermediates for medicines and pesticides, and in the production of feed additives and synthetic fra

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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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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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