Interesting facts
Interesting Facts about Methyl 4-(2,4-dichlorophenoxy)butanoate
Methyl 4-(2,4-dichlorophenoxy)butanoate is an intriguing chemical compound that merges the functionalities of esters with notable biological activity. Here are some captivating points to consider:
- Biological Relevance: This compound is often studied due to its potential role in agricultural applications, particularly as a herbicide. Compounds with similar structures have shown efficacy in controlling various weed species, promoting its significance in crop management.
- Mechanism of Action: Ester derivatives like methyl 4-(2,4-dichlorophenoxy)butanoate may act by disrupting hormonal pathways in plants, particularly affecting auxin regulation. This insight is crucial for developing selective herbicides.
- Synthesis Pathways: The synthesis of this compound can involve several methods, including the reaction of 2,4-dichlorophenol with specific butanoic acid derivatives. Understanding these pathways can enhance the efficiency of agricultural chemical production.
- Environmental Impact: An essential consideration for compounds used in agriculture is their environmental footprint. Researchers actively study their degradation products to assess their long-term effects on soil and water ecosystems.
- Regulatory Considerations: Given its functionality and potential use, methyl 4-(2,4-dichlorophenoxy)butanoate is likely subject to regulatory scrutiny to ensure its safe usage within agricultural practices, balancing effectiveness with ecological safety.
As a chemist or avid student, exploring such compounds can lead to a better understanding of their multifaceted roles in both science and industry. The blend of chemistry with practical applications underscores the importance of these substances in advancing sustainable agricultural practices.
Synonyms
Methyl 4-(2,4-dichlorophenoxy)butanoate
18625-12-2
2,4-DB-methyl ester
Butanoic acid, 4-(2,4-dichlorophenoxy)-, methyl ester
2,4-dichlorophenoxybutyric acid, methyl ester
DTXSID70171872
Butyric acid, 4-(2,4-dichlorophenoxy)-, methyl ester
2,4-DB methyl ester
KBio2_002376
2,4-DB-methylester
Spectrum_001863
SpecPlus_000474
Spectrum2_001852
Spectrum3_000837
Spectrum4_000677
Spectrum5_001988
BSPBio_002393
KBioGR_001113
KBioSS_002380
SPECTRUM330045
DivK1c_006570
SPBio_001664
CHEMBL1448913
DTXCID5094363
SCHEMBL12998521
KBio1_001514
KBio2_004944
KBio2_007512
KBio3_001893
NKXSNMCGZZWMMW-UHFFFAOYSA-N
TAA62512
CCG-39390
MFCD00142813
AKOS005072666
FA-0729
Methyl 4-(2,4-dichlorophenoxy)butyrate
NCGC00094535-01
NCGC00094535-02
NCGC00094535-03
CS-0336692
NS00100921
4-(2,4-Dichlorophenoxy)butyric acid methyl ester
Butanoic acid,4-(2,4-dichlorophenoxy)-,methyl ester
2,4-DB-methyl ester, PESTANAL(R), analytical standard
621-284-8
Solubility of Methyl 4-(2,4-dichlorophenoxy)butanoate
Methyl 4-(2,4-dichlorophenoxy)butanoate, with the chemical formula C11H12Cl2O3, exhibits notable properties concerning its solubility. This organic compound can be analyzed based on its formulation which contains both hydrophobic and hydrophilic components:
As a result, methyl 4-(2,4-dichlorophenoxy)butanoate demonstrates:
In practical applications, understanding this solubility balance is crucial for formulation and efficacy, especially in agricultural and pharmaceutical contexts. As with many organic compounds, factors such as temperature and pH can further influence its solubility properties:
In summary, while methyl 4-(2,4-dichlorophenoxy)butanoate has limitations in water solubility, its behavior in various organic solvents is vital for its application.