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Hydratropic acid

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Identification
Molecular formula
C10H12O2
CAS number
547-63-7
IUPAC name
2-methyl-4-phenyl-butanoic acid
State
State

At room temperature, hydratropic acid is in a solid state, presenting as crystalline or powder form.

Melting point (Celsius)
72.00
Melting point (Kelvin)
345.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
164.21g/mol
Molar mass
164.2070g/mol
Density
1.0783g/cm3
Appearence

Hydratropic acid typically appears as a white crystalline solid. Its crystals are often fine and needle-like, and it may also be available in powdered form for laboratory use.

Comment on solubility

Solubility of 2-methyl-4-phenyl-butanoic acid

2-methyl-4-phenyl-butanoic acid, a branched-chain carboxylic acid, exhibits specific solubility characteristics that are worthy of discussion. This compound is generally soluble in organic solvents due to its hydrophobic phenyl group and moderate alkyl chain. However, its solubility in water is limited.

When considering the solubility of 2-methyl-4-phenyl-butanoic acid, here are some key points:

  • Polar vs. Nonpolar: The compound has both polar (the carboxylic acid group) and nonpolar (the hydrocarbon chains) characteristics.
  • Water Solubility: It has poor solubility in water due to its large hydrophobic portion, which hinders extensive hydrogen bonding with water molecules.
  • Organic Solvents: 2-methyl-4-phenyl-butanoic acid is more soluble in nonpolar and slightly polar organic solvents, such as ethanol and acetone.

In conclusion, while 2-methyl-4-phenyl-butanoic acid showcases a degree of versatility in solubility across various solvents, its hydrophobic nature restricts its interaction with water, making it preferred for use in nonpolar systems.

Interesting facts

Interesting Facts About 2-methyl-4-phenyl-butanoic Acid

2-methyl-4-phenyl-butanoic acid is a fascinating compound in the realm of organic chemistry, with several noteworthy characteristics and applications. Here are some key points:

  • Structural Composition: The compound features a butanoic acid backbone with a methyl and phenyl substituent, contributing to its unique chemical properties. This structure not only influences its reactivity but also its biological activity.
  • Pharmaceutical Relevance: Compounds like 2-methyl-4-phenyl-butanoic acid have garnered attention in medicinal chemistry. Their structural properties can play crucial roles in drug development, particularly in targeting specific pathways in metabolic processes.
  • Taste and Smell: Research on the sensory aspects of similar compounds suggests that the flavor profiles could be intriguing. The presence of a phenyl group can enhance aroma characteristics, making these types of acids potentially useful in flavoring and fragrance industries.
  • Biological Impacts: Some studies suggest that the presence of butanoic acid chains can influence cellular processes, such as those in fatty acid metabolism. Investigating how 2-methyl-4-phenyl-butanoic acid interacts with cellular pathways could lead to breakthroughs in understanding metabolic disorders.
  • Synthesis Methods: The synthesis of this compound involves various organic reactions, ranging from straightforward acid catalyzed reactions to more complex multi-step processes. This provides students and researchers with valuable experience in practical organic synthesis techniques.
  • Potential for Derivatives: The versatile structure opens doors to many derivatives, which can exhibit different biological activities or chemical behaviors. This suggests a potential for innovation in synthesizing new compounds with targeted properties.

As a result, 2-methyl-4-phenyl-butanoic acid stands as a notable subject of study within the field, bridging the gap between fundamental chemistry and applied science. The insights gleaned from its study continue to inspire curiosity and exploration in both academic and industrial chemistry.

Synonyms
2-methyl-4-phenylbutanoic acid
1949-41-3
2-Methyl-4-phenyl-butyric acid
BUTYRIC ACID, 2-METHYL-4-PHENYL-
NSC 402998
BRN 1911280
DTXSID501306426
2-09-00-00363 (Beilstein Handbook Reference)
DTXCID401736389
622-537-5
alpha-Methylbenzenebutyric acid
NSC-402998
alpha-Methylbenzenebutanoic Acid
MFCD00796471
NSC402998
MNX7BV7UFZ
|A-Methylbenzenebutyric acid
2-methyl-4-phenylbutanoicacid
SCHEMBL473576
OCKZHEXBLOOGOC-UHFFFAOYSA-N
Benzenebutanoic acid, alpha-methyl-
AKOS010488656
BS-50099
DB-377617
CS-0196931
E73969
EN300-1863868
A1-08676