3-Hydroxypropionic acid
Chemical compound From Wikipedia, the free encyclopedia
3-Hydroxypropionic acid is a carboxylic acid, specifically a beta hydroxy acid. It is an acidic viscous liquid with a pKa of 4.9.[2] It is very soluble in water, soluble in ethanol and diethyl ether. Upon distillation, it dehydrates to form acrylic acid, and is occasionally called hydracrylic acid
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| Names | |
|---|---|
| Preferred IUPAC name
3-Hydroxypropanoic acid | |
| Other names
3-Hydroxypropionic acid Hydracrylic acid Ethylene lactic acid | |
| Identifiers | |
3D model (JSmol) |
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| 773806 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.007.250 |
| EC Number |
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| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C3H6O3 | |
| Molar mass | 90.08 g/mol |
| Melting point | <25 °C 143 °C (sodium salt) |
| Boiling point | Decomposes |
| Very soluble | |
| Acidity (pKa) | 4.87[2] |
| Related compounds | |
Related carboxylic acids |
acetic acid glycolic acid propionic acid lactic acid malonic acid butyric acid hydroxybutyric acid |
Related compounds |
1-propanol 2-propanol propionaldehyde acrolein |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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3-Hydroxypropionic acid is used in the industrial production of various chemicals such as acrylates.
Synthesis
3-Hydroxypropionic acid can be obtained by base-induced hydration of acrylic acid followed by reacidification. Another synthesis involves cyanation of ethylene chlorohydrin followed by hydrolysis of the resulting nitrile. Hydrolysis of propiolactone is yet another route.[3] Propiolactone, the dehydrated derivative of 3-hydroxypropionic acid, is produced by reaction of ketene and formaldehyde.[4]
3-Hydroxypropionic acid is listed as one of the "top" chemicals that could be produced from renewable resources. In particular, it could be produced by manipulation of glycerol, but this technology has not reached a commercial stage.[5] It can also be produced from glucose via pyruvate and malonyl coenzyme A.[4][6]
Potential applications
3-Hydroxypropionic acid is of interest as a bio-derived precursor to acrylic acid.[5]
The polyester poly(3-hydroxypropionic acid) is a biodegradable polymer.[7] The method combines the high-molecular weight and control aspects of ring-opening polymerization with the commercial availability of the beta hydroxy acid, 3-hydroxypropionic acid which is abbreviated as 3-HP. Since 3-HPA can be derived from biological sources, the resulting material, poly(3-hydroxypropionic acid) or P(3-HPA), is biorenewable.
Genetically encoded 3-hydroxypropionic acid inducible system
3-Hydroxypropionic acid can be produced by engineered microbes.[8]
A genetically encoded 3-hydroxypropionic acid inducible system has been characterized in bacteria demonstrating that such system in combination with fluorescent reporter protein can be utilized as a biosensor to measure intracellular and extracellular 3-HP concentrations by fluorescence output.[9]
See also
- Lactic acid (2-hydroxypropanoic acid)
- listed as hydracrylic acid in the Merck index, 12th Edition
References
External links
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