Interesting facts
Interesting Facts about 2,2-Dimethylbutanoic Acid
2,2-dimethylbutanoic acid is a fascinating molecule within the family of carboxylic acids, known for its unique structure and a variety of applications. Here are some intriguing aspects of this compound:
- Structural Uniqueness: The molecule features a branched structure, which distinguishes it from straight-chain carboxylic acids. This branching occurs at the second carbon of the butanoic acid backbone, resulting in enhanced steric effects and influencing its reactivity.
- Synthesis and Reactions: 2,2-dimethylbutanoic acid can be synthesized through several methods, including the oxidation of the corresponding alcohol or the carbonylation of certain alkenes. It undergoes typical carboxylic acid reactions such as esterification and acid-base reactions, showcasing its versatility in organic synthesis.
- Biological Relevance: While this compound may not be as well-known in biological contexts compared to other acids, its structural similarities to common fatty acids hint at possible roles in metabolic pathways and biochemical studies.
- Industrial Applications: The compound can serve as an intermediate in the production of various chemical products, including pharmaceuticals, agrochemicals, and plastics. Its branched structure contributes to distinct properties that can be leveraged in material science.
- Safety Considerations: As with many organic acids, proper handling and safety precautions are essential. Understanding the acid's reactivity and potential hazards contributes to safe laboratory practices.
In summary, 2,2-dimethylbutanoic acid offers a blend of unique structural properties and diverse applications, making it a compound of interest for chemists and researchers alike. Its intriguing characteristics highlight the importance of studying branched carboxylic acids, paving the way for innovative solutions across various disciplines.
Synonyms
2,2-Dimethylbutanoic acid
2,2-DIMETHYLBUTYRIC ACID
595-37-9
CHEBI:38649
DTXSID0032811
EINECS 209-865-0
alpha,alpha-Dimethylbutyric acid
DTXCID8012811
alpha,alpha-Dimethylbutanoic acid
EC 209-865-0
NSC 16045
ST-20 compound
2,2-DMB
209-865-0
Butanoic acid, 2,2-dimethyl-
Dimebutic Acid
2,2-dimethyl-butyric acid
2,2-dimethyl-butanoic acid
2,2-Dimethyl Butyric Acid
2,2-Dimethyl butanoic acid
Butyric acid, 2,2-dimethyl-
2,2-dimethylbutyric-d11 acid
1219804-04-2
dimethyl ethyl acetic acid
MFCD00004200
NSC-16045
AY606CN05O
.alpha.,.alpha.-Dimethylbutyric acid
.alpha.,.alpha.-Dimethylbutanoic acid
NSC-741804
Neohexanoic acid
UNII-AY606CN05O
Acido dimebutico
Acide dimebutique
2,2-dimethylbutyrate
Dimebutic acid [INN]
2,2-Dimethylbutanoicacid
2.2-Dimethylbutyric acid
Butanoic acid,2-dimethyl-
SCHEMBL47533
MLS002174247
CHEMBL286013
2,2-Dimethylbutyric acid, 96%
HMS3039B09
NSC16045
2,2'-DIMETHYLPROPIONIC ACID
Tox21_200740
BDBM50566497
LMFA01020078
AKOS009158866
CS-W016597
NCGC00090948-01
NCGC00090948-02
NCGC00258294-01
CAS-595-37-9
DA-69626
DS-14471
SMR001261422
DB-027513
D2429
NS00003624
EN300-64847
BRD-K44963273-001-06-9
Q27117928
Z995036360
InChI=1/C6H12O2/c1-4-6(2,3)5(7)8/h4H2,1-3H3,(H,7,8
Solubility of 2,2-Dimethylbutanoic Acid
2,2-Dimethylbutanoic acid, with the chemical formula C6H12O2, exhibits interesting solubility characteristics that are important to understand.
This compound is an alkyl carboxylic acid, which generally affects its solubility in various solvents:
However, the solubility in water may not be very high because:
In summary, 2,2-dimethylbutanoic acid demonstrates a balance of solubility in both polar and nonpolar solvents, making it versatile for various chemical applications.