Page last updated: 2024-12-09

1-dodecyl-3-methylimidazolium

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

## 1-Dodecyl-3-methylimidazolium: A Versatile Ionic Liquid

1-Dodecyl-3-methylimidazolium, often abbreviated as [C12mim]+, is a **cation** found in a family of compounds known as **ionic liquids**. These are salts that are liquid at or below 100°C, possessing unique properties that have made them a hot topic in research.

**Key features of [C12mim]+:**

* **Long alkyl chain (dodecyl):** The 12-carbon chain attached to the imidazolium ring makes [C12mim]+ **hydrophobic**, allowing it to interact with nonpolar substances.
* **Imidazolium ring:** This ring provides a **hydrophilic** site, enabling the cation to dissolve in polar solvents.
* **High ionic conductivity:** Like other ionic liquids, [C12mim]+ exhibits high ionic conductivity, making it suitable for applications in **electrochemistry**.
* **Wide electrochemical window:** The large electrochemical window allows for a range of electrochemical reactions to occur without decomposition.
* **Low vapor pressure:** This property makes it **environmentally friendly** and less volatile compared to traditional organic solvents.

**Importance in research:**

The unique properties of [C12mim]+ make it a versatile tool for various research areas:

* **Green chemistry:** Its low vapor pressure and high thermal stability make it a potential replacement for harmful organic solvents in many chemical processes.
* **Catalysis:** [C12mim]+ can act as a catalyst or reaction medium in various organic reactions, improving efficiency and selectivity.
* **Electrochemistry:** Its high conductivity and wide electrochemical window make it suitable for applications in batteries, fuel cells, and electrochemical sensors.
* **Materials science:** The long alkyl chain allows for the formation of self-assembled structures, leading to applications in nanomaterials and coatings.
* **Biotechnology:** [C12mim]+ can interact with biomolecules, offering potential applications in drug delivery and biocatalysis.

**Current research:**

Active research focuses on:

* **Tuning its properties:** By modifying the anion or alkyl chain length, researchers can adjust the properties of [C12mim]+ for specific applications.
* **Understanding its interactions:** Studies explore its interactions with different materials and biomolecules, paving the way for new applications.
* **Developing new synthetic routes:** Efficient and cost-effective synthesis methods are crucial for large-scale applications.

**Overall:**

[C12mim]+ is a promising ionic liquid with a wide range of potential applications. Ongoing research aims to unlock its full potential and contribute to advancements in various fields.

1-dodecyl-3-methylimidazolium: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-dodecyl-3-methylimidazolium : A 1-alkyl-3-methylimidazolium in which the alkyl substituent at C-1 is dodecyl. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID2734228
CHEMBL ID1198668
CHEBI ID61349
SCHEMBL ID92755
MeSH IDM0511806

Synonyms (14)

Synonym
1h-imidazolium, 3-dodecyl-1-methyl-
1-dodecyl-3-methyl-imidazol-1-ium
1-dodecyl-3-methyl-1h-imidazol-3-ium
1-dodecyl-3-methylimidazolium
[c12mim]
CHEBI:61349 ,
CHEMBL1198668
46928-10-3
SCHEMBL92755
DTXSID6048090
Q27131053
1-(dodecyl)-3-methylimidazolium
CS9VNU3TN8
3-dodecyl-1-methyl-1h-imidazolium
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
1-alkyl-3-methylimidazoliumAn imidazolium ion with an alkyl substituent at the 1-position and a methyl substituent at the 3-position.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (5.00)29.6817
2010's17 (85.00)24.3611
2020's2 (10.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.25

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.25 (24.57)
Research Supply Index3.04 (2.92)
Research Growth Index5.29 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.25)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]