2, 4-Pentanedione refers to an organic compound that survives in two tautomeric appearances that are treated as a single compound and they interconvert rapidly. It is a colorless liquid that is a forerunner to acetylacetone (acac).
The compound’s chemical formula is CH3COCH2OCCH3. The enol and keto forms of acetylacetone coexist in solution. They further form tautomers. The hydrogen atom is shared uniformly between two oxygen atoms as the enol form has C2v symmetry. During the gas stage, the equilibrium constant is 11.7.
It favors the enol form. The two tautomeric forms are simply distinguished by IR spectroscopy, NMR spectroscopy, and other methods. In nonpolar solvents, the equilibrium constant remains high. On the other hand, the keto form stays favorable in polar, water, and hydrogen-bonding solvents.
The enol form is the vinylogous analogue of carboxylic acid. By uses, the global 2, 4-Pentanedione (CAS 123-54-6) market can be segmented by pesticides, solvent, paint drier and lubricant additive.
2, 4-Pentanedione is the adaptable bifunctional precursor to heterocycles as both keto groups go through condensation. Pyrazoles is produced by hydrazine reactions. On the other hand, urea gives pyrimidines.
Biodegradation of 2, 4-Pentanedione includes an enzyme breakdown. In addition, the enzyme acetylacetone dioxygenase slices the carbon-bond of acetylacetone. It forms 2-oxopropanal and acetate. The enzyme is proven to bind zinc and is iron dependent.
2, 4-Pentanedione anion creates complexes with numerous transitional metal ions. The usual technique of synthesis is to respond the metal ion in the existence of base. It shifts the equilibrium the favor of the complex and also assists in the elimination of the proton.
Sometimes, the chelate effect is very strong and no supplementary base in needed to produce the complex. The metal complex is sometimes insoluble in water as it takes no electrical charge.
It can be soluble in nonpolar organic solvents. The global 2, 4-Pentanedione (CAS 123-54-6) market can be further analyzed by manufacturing technology, applications, regions, competitive landscape, and statistical analysis.
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Table of Contents:
Chapter One Introduction of 2,4-Pentanedione Industry
1.1 Brief Introduction of 2,4-Pentanedione
1.2 Development of 2,4-Pentanedione Industry
1.3 Status of 2,4-Pentanedione Industry
Chapter Two Manufacturing Technology of 2,4-Pentanedione
2.1 Development of 2,4-Pentanedione Manufacturing Technology
2.2 Analysis of 2,4-Pentanedione Manufacturing Technology
2.3 Trends of 2,4-Pentanedione Manufacturing Technology
Chapter Three Analysis of Global Key Manufacturers
3.1 Company A
3.2 Company B
3.3 Company C
3.4 Company D
3.5 Company E
3.6 Company F
3.7 Company G
3.8 Company H
The compound’s chemical formula is CH3COCH2OCCH3. The enol and keto forms of acetylacetone coexist in solution. They further form tautomers. The hydrogen atom is shared uniformly between two oxygen atoms as the enol form has C2v symmetry. During the gas stage, the equilibrium constant is 11.7.
It favors the enol form. The two tautomeric forms are simply distinguished by IR spectroscopy, NMR spectroscopy, and other methods. In nonpolar solvents, the equilibrium constant remains high. On the other hand, the keto form stays favorable in polar, water, and hydrogen-bonding solvents.
The enol form is the vinylogous analogue of carboxylic acid. By uses, the global 2, 4-Pentanedione (CAS 123-54-6) market can be segmented by pesticides, solvent, paint drier and lubricant additive.
2, 4-Pentanedione is the adaptable bifunctional precursor to heterocycles as both keto groups go through condensation. Pyrazoles is produced by hydrazine reactions. On the other hand, urea gives pyrimidines.
Biodegradation of 2, 4-Pentanedione includes an enzyme breakdown. In addition, the enzyme acetylacetone dioxygenase slices the carbon-bond of acetylacetone. It forms 2-oxopropanal and acetate. The enzyme is proven to bind zinc and is iron dependent.
2, 4-Pentanedione anion creates complexes with numerous transitional metal ions. The usual technique of synthesis is to respond the metal ion in the existence of base. It shifts the equilibrium the favor of the complex and also assists in the elimination of the proton.
Sometimes, the chelate effect is very strong and no supplementary base in needed to produce the complex. The metal complex is sometimes insoluble in water as it takes no electrical charge.
It can be soluble in nonpolar organic solvents. The global 2, 4-Pentanedione (CAS 123-54-6) market can be further analyzed by manufacturing technology, applications, regions, competitive landscape, and statistical analysis.
To Read other reports of this category:
http://www.radiantinsights.com/catalog/chemicals
Table of Contents:
Chapter One Introduction of 2,4-Pentanedione Industry
1.1 Brief Introduction of 2,4-Pentanedione
1.2 Development of 2,4-Pentanedione Industry
1.3 Status of 2,4-Pentanedione Industry
Chapter Two Manufacturing Technology of 2,4-Pentanedione
2.1 Development of 2,4-Pentanedione Manufacturing Technology
2.2 Analysis of 2,4-Pentanedione Manufacturing Technology
2.3 Trends of 2,4-Pentanedione Manufacturing Technology
Chapter Three Analysis of Global Key Manufacturers
3.1 Company A
3.2 Company B
3.3 Company C
3.4 Company D
3.5 Company E
3.6 Company F
3.7 Company G
3.8 Company H
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