CAS 123-76-2
:Levulinic acid
Description:
Levulinic acid, with the CAS number 123-76-2, is a five-carbon ketocarboxylic acid that is derived from the degradation of carbohydrates. It is typically a colorless to pale yellow liquid with a slightly sweet odor. Levulinic acid is soluble in water, alcohols, and many organic solvents, making it versatile for various applications. Its molecular formula is C5H8O3, and it features both a carboxylic acid and a ketone functional group, which contribute to its reactivity and potential as a building block in organic synthesis. Levulinic acid is recognized for its potential as a platform chemical in the production of biofuels, pharmaceuticals, and biodegradable polymers. Additionally, it exhibits antimicrobial properties and can be used as a food preservative. Its ability to undergo various chemical transformations, such as esterification and reduction, further enhances its utility in chemical processes. Overall, levulinic acid is an important compound in the context of green chemistry and sustainable development.
Formula:C5H8O3
InChI:InChI=1S/C5H8O3/c1-4(6)2-3-5(7)8/h2-3H2,1H3,(H,7,8)
InChI key:InChIKey=JOOXCMJARBKPKM-UHFFFAOYSA-N
SMILES:C(CC(O)=O)C(C)=O
Synonyms:- 3-Acetylpropanoic acid
- 3-Acetylpropionic acid
- 3-Oxobutanecarboxylic acid
- 4-Ketovaleric acid
- 4-Oxopentanoic acid
- 4-Oxovaleriansaure
- 4-Oxovaleric Acid
- Acide 4-oxovalerique
- Acido 4-Oxovalerico
- Laevulinic acid
- Laevulinsaeure
- Lev-OH
- Levulic acid
- Levulinic acid
- Nsc 3716
- β-Acetylpropionic acid
- γ-Ketovaleric acid
- laevulic acid
- calcium bis(4-oxopentanoate)
- Pentanoic acid, 4-oxo-
- 4-Ketopentanoic acid
- sodium 4-oxopentanoate
- Levulinic acid,(4-Ketopentanoic acid
- 2-methyl-3-oxobutanoic acid
- See more synonyms
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Found 10 products.
Levulinic Acid
CAS:Formula:C5H8O3Purity:>97.0%(GC)(T)Color and Shape:White or Colorless to Light yellow powder to lump to clear liquidMolecular weight:116.12Levulinic acid, 98%
CAS:<p>Mainly used as an intermediate for medicines, agricultural chemical and organic synthesis. Used as raw material of perfume, modifier and solvent of plastics. It is also employed as an additive of polymer, paints and lubricating oil. Also used as a surfactant and auxiliary for making printing ink, r</p>Formula:C5H8O3Purity:98%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:116.12Levulinic acid
CAS:<p>Levulinic acid (4-Oxovaleric acid), derived from the degradation of cellulose, is a precursor for the synthesis of biofuels, such as ethyl levulinate.</p>Formula:C5H8O3Purity:99.76%Color and Shape:Liquid PelletslargecrystalsMolecular weight:116.12Levulinic Acid
CAS:Controlled Product<p>Applications Levulinic Acid is derived from the degredation of cellulose and is a potential precursor to biofuels. Levulinic acid is also a photosensitizer for photodynamic therapy.<br>References Serrano-Ruiz, J.C., et al.: Catalysis., 195, 162 (2012); Liedtke, A.J. et al.: Tetrahedron., 68, 10049 (2012);<br></p>Formula:C5H8O3Color and Shape:Light Yellow MeltedMolecular weight:116.12Levulinic acid
CAS:<p>Levulinic acid is an organic compound, which is derived from the acid hydrolysis of biomass, such as lignocellulosic materials. Its chemical structure makes it a pivotal platform chemical with potential for diverse transformations. Levulinic acid functions as a building block for various chemical synthesis processes, facilitating the production of numerous derivatives including pharmaceuticals, agrochemicals, plasticizers, and biofuels.</p>Formula:C5H8O3Purity:Min. 97.0 Area-%Molecular weight:116.12 g/molLevulinic acid
CAS:<p>Levulinic acid is a dicarboxylic acid that is resistant to the formation of the levulinate ester. In vitro, it has been shown to have a synergistic effect with other antibiotics such as erythromycin and cefazolin against bacteria in experimental models. The mechanism of this synergistic effect is not known, but may be due to inhibition of bacterial cell wall synthesis. Levulinic acid can also be used as an injection solution or magnesium salt for surface methodology experiments. The rate of reaction with magnesium is slow, and the reactivity is similar to that of levulinate. Kinetic studies have shown that the rate-determining step in the reaction between levulinic acid and magnesium chloride is the binding of MgCl2 to LHA (levulinic acid). This binding also reacts slowly with water and formaldehyde.</p>Formula:C5H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:116.12 g/mol4-Oxopentanoic acid
CAS:Formula:C5H8O3Purity:97%Color and Shape:Solid, Low Melting SolidMolecular weight:116.116Levulinic Acid
CAS:Carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids andtheir derivFormula:C5H8O3Molecular weight:116.04734









