Allyl alcohol is an organic compound with the chemical formula C3H6O. It belongs to the class of alcohols and contains both a hydroxyl group (-OH) and an allyl group (-CH2CH=CH2). It is an important chemical intermediate used in various industries.
Allyl chloride, also known as 3-chloropropene, is an organic compound with the chemical formula C3H5Cl. It is a colorless to pale yellow liquid that holds significance in the field of organic chemistry due to its reactivity and industrial applications.
Ammonium chloride (NH4Cl) is a chemical compound composed of ammonia (NH3) and hydrochloric acid (HCl). It exists as a white crystalline solid with a characteristic salty taste and is commonly known as sal ammoniac.
Ammonium nitrate (NH4NO3) is a chemical compound composed of ammonium ions (NH4+) and nitrate ions (NO3-). It is a colorless, crystalline substance widely used in various applications, including agriculture, industry, and explosives.
Ammonium sulfate is a chemical compound with the formula (NH4)2SO4. It is commonly encountered as a white, crystalline powder or granular substance. It has emerged as a significant compound during the 19th century produced from ammonia found in coke-oven gas.
4-(N-Methylamino)phenol, 4-(N,N-Dimethylamino)phenol, 4-Hydroxyacetanilide, 4-Methoxyaniline, 4-Ethoxyaniline, 4-Ethoxyacetanilide, 5-Aminosalicylic Acid, N-(4-Hydroxyphenyl)glycine, 4-Amino-2,6-dichlorophenol
Aminophenols have been gaining significant commercial importance, both as standalone substances and as crucial components in the chemical and dye sectors.
Aromatic amines are produced by three types of reactions:
Reductions: using metallic elements like Iron (Fe), Zinc (Zn), Tin (Sn), Aluminum (Al), or their corresponding salts; sulfur-containing compounds; electrochemical procedures; and catalytic hydrogenation.
Nucleophilic substitutions: involving the exchange of substituents like halogen, hydroxyl, alkoxy, and sulfonic groups.
Rearrangements and degradations: including transformations such as the benzidine and Beckmann rearrangements, along with the Schmidt and Hofmann degradations.
It should be noted that the first two reaction types are more important. Chemical rearrangements and degradations rarely result in pure reaction products with high yields.
The primary method of producing aldehydes is oxo synthesis, achieved by mild oxidation (dehydrogenation) of primary alcohols and specialized olefin oxidation processes. In the essential oils of various plants, trace amounts of aldehydes occur naturally. Acetaldehyde, a byproduct of alcohol fermentation, forms by the decarboxylation of the intermediary pyruvic acid.
1,4-butanediol (often abbreviated as 1,4-BDO) is a chemical compound with the molecular formula C4H10O2. It is a colorless and odorless liquid that belongs to the family of diols, which are compounds that contain two hydroxyl (OH) groups.
Production of aliphatic alcohols occurs by various industrial processes, some of which are listed below:
Synthesis from carbon monoxide and hydrogen (C1)
Oxo synthesis, often accompanied by hydrogenation of initially formed aldehydes (C3 - C20)
Hydrogenation of aldehydes, carboxylic acids, or esters
Aldol condensation of lower aldehydes followed by hydrogenation of the alkenals (C3 → C6, C4 → C8, C8 → C16)
Oxidation of trialkylaluminum compounds (Ziegler process)
Oxidation of saturated hydrocarbons
Hydration of olefins (C2–C4)
Homologation of alcohols
Hydrocarbonylation by the Reppe process
Hydrocarboxymethylation
Fermentation processes (C2–C5)
Guerbet process
Adipic acid, also known as hexanedioic acid or 1,4-butanedicarboxylic acid, is an organic compound with the formula C6H10O4. It is a widely used aliphatic dicarboxylic acid that appears as a white crystalline solid.