• Source: Alpha hydroxycarboxylic acid

Alpha hydroxy carboxylic acids, or α-hydroxy carboxylic acids (AHAs), are a group of carboxylic acids featuring a hydroxy group located one carbon atom away from the acid group. This structural aspect distinguishes them from beta hydroxy acids, where the functional groups are separated by two carbon atoms. Notable AHAs include glycolic acid, lactic acid, mandelic acid, and citric acid.
α-Hydroxy acids are stronger acids compared to their non-alpha hydroxy counterparts, a property enhanced by internal hydrogen bonding. AHAs serve a dual purpose; industrially, they are utilized as additives in animal feed and as precursors for polymer synthesis. In cosmetics, they are commonly used for their ability to chemically exfoliate the skin.




Uses


The synthesis and utilization of polymers based on lactic acid, including polylactic acid (PLA) and its cyclic ester lactide, are used in the creation of biodegradable materials such as medical implants, drug delivery systems, and sutures. Similarly, glycolic acid serves as a foundation for the development of poly(glycolic acid), spelled polyglycolide (PGA), a polymer distinguished by its high crystallinity, thermal stability, and mechanical strength, despite its synthetic origins. Both PLA and PGA are fully biodegradable.
Furthermore, mandelic acid, another alpha hydroxy acid, when combined with sulfuric acid produces 'SAMMA', obtained via condensation with sulfuric acid. Early laboratory work performed in 2002 and 2007 against notable pathogens such as the human immunodeficiency virus (HIV) and the herpes simplex virus (HSV) suggest SAMMA warrants further investigation as a topical microbicide to prevent vaginal sexually-transmitted infection transmission.
2-Hydroxy-4-(methylthio)butyric acid, alpha hydroxy carboxylic acid, is used commercially in a racemic mixture to substitute for methionine in animal feed.




Occurrence


Aldonic acids, a type of sugar acid, are a class of naturally occurring hydroxycarboxylic acids. They have the general chemical formula, HO2C(CHOH)nCH2OH. Gluconic acid, a particularly common aldonic acid, the oxidized derivative of glucose.
2-Hydroxy-4-(methylthio)butyric acid is an intermediate in the biosynthesis of 3-dimethylsulfoniopropionate, precursor to natural dimethyl sulfide.




Synthesis


One common synthesis route involves the hydrolysis of α-halocarboxylic acids, readily available precursors, to produce 2-hydroxycarboxylic acids. For instance, the production of glycolic acid typically follows this method, utilizing a base-induced reaction, followed by acid workup. Similarly, unsaturated acids and fumarate and maleate esters undergo hydration to yield malic acid derivatives from esters, and 3-hydroxypropionic acid from acrylic acid.

R−CH(Cl)CO2H + H2O → R−CH(OH)CO2H + HCl
Another synthetic pathway for α-hydroxy acids involves the addition of hydrogen cyanide to ketones or aldehydes, followed by the acidic hydrolysis of the cyanohydrin intermediate.

R−CHO + HCN → R−CH(OH)CN
R−CH(OH)CN + 2H2O → R−CH(OH)CO2H + NH3
Furthermore, specialized synthetic routes include the reaction of dilithiated carboxylic acids with oxygen, followed by aqueous workup.

R−CHLiCO2Li + O2 → R−CH(O2Li)CO2Li
R−CH(O2Li)CO2Li + H+ → R−CH(OH)CO2H + 2Li+ + ...
Additionally, α-keto aldehydes can be transformed into α-hydroxy acids through the Cannizzaro reaction.

R−C(O)CHO + 2OH− → R−CH(OH)CO−2 + H2O




Uses


α-Hydroxy acids, such as glycolic acid, lactic acid, citric acid, and mandelic acid, serve as precursors in organic synthesis, playing a role in the industrial-scale preparation of various compounds. These acids are used when synthesizing aldehydes through oxidative cleavage. α-Hydroxy acids are particularly prone to acid-catalyzed decarbonylation, yielding carbon monoxide, a ketone or aldehyde, and water as by-products.




Safety


Alpha hydroxy acids are generally safe when used on the skin as a cosmetic agent using the recommended dosage. The most common side-effects are mild skin irritations, redness and flaking. The United States Food and Drug Administration (FDA) and Cosmetic Ingredient Review expert panels both suggest that alpha hydroxy acids are safe to use as long as they are sold at low concentrations, pH levels greater than 3.5, and include thorough safety instructions.
The FDA has warned consumers that care should be taken when using alpha hydroxy acids after an industry-sponsored study found that they can increase the likelihood of sunburns. This effect is reversible after stopping the use of alpha hydroxy acids. Other sources suggest that glycolic acid, in particular, may protect from sun damage.




See also


Beta hydroxy acid
Hydroxybutyric acid
Omega hydroxy acid




Further reading


Atzori L, Brundu MA, Orru A, Biggio P (March 1999). "Glycolic acid peeling in the treatment of acne". Journal of the European Academy of Dermatology and Venereology. 12 (2): 119–22. doi:10.1111/j.1468-3083.1999.tb01000.x. PMID 10343939. S2CID 9721678.
"Alpha Hydroxy Acids for Skin Care". Cosmetic Dermatology, Supplement: 1–6. October 1994.
Kalla G, Garg A, Kachhawa D (2001). "Chemical peeling--glycolic acid versus trichloroacetic acid in melasma". Indian Journal of Dermatology, Venereology and Leprology. 67 (2): 82–4. PMID 17664715.
Kempers S, Katz HI, Wildnauer R, Green B (June 1998). "An evaluation of the effect of an alpha hydroxy acid-blend skin cream in the cosmetic improvement of symptoms of moderate to severe xerosis, epidermolytic hyperkeratosis, and ichthyosis". Cutis. 61 (6): 347–50. PMID 9640557.




References






External links


U.S. Food and Drug Administration: Alpha Hydroxy Acids in Cosmetics

Kata Kunci Pencarian:

• Uranium
• Alpha hydroxycarboxylic acid
• Hydroxycarboxylic acid
• Beta hydroxycarboxylic acid
• Stability constants of complexes
• Hydroxycarboxylic acid receptor 2
• Pechini process
• Lactic acid
• Malic acid
• Hydroxybutyric acid
• Glycolic acid