Page last updated: 2024-12-08

11-mercaptoundecanoic acid

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

## 11-Mercaptoundecanoic acid (MUA)

**11-Mercaptoundecanoic acid (MUA)** is a long-chain fatty acid with a thiol group (-SH) at the end of the molecule. It's a colorless to pale yellow liquid at room temperature and has a faint odor.

**Importance in Research:**

MUA plays a crucial role in various research fields, including:

**1. Material Science:**

* **Self-Assembled Monolayers (SAMs):** MUA is widely used to form SAMs on gold surfaces. The thiol group readily binds to gold, creating a well-ordered, densely packed monolayer with controllable surface properties.
* **Nano- and Microscale Fabrication:** MUA is used as a building block for creating complex nanostructures and microstructures through techniques like dip-pen nanolithography.
* **Biocompatibility and Surface Modification:** MUA can be functionalized with various molecules to modify the surface properties of materials for applications in biomaterials, drug delivery, and biosensors.

**2. Chemistry:**

* **Organic Synthesis:** MUA serves as a versatile building block for synthesizing various organic compounds, including polymers, peptides, and other functional molecules.
* **Analytical Chemistry:** MUA is used in analytical techniques like electrochemistry and chromatography due to its unique chemical properties.

**3. Biology and Medicine:**

* **Bioimaging:** MUA can be used to label cells and biomolecules for microscopic imaging and tracking.
* **Drug Delivery:** MUA-based nanoparticles can be designed to deliver drugs and other therapeutic agents to specific target sites.
* **Biocompatible Materials:** MUA can be used to modify the surface of biomedical devices to improve biocompatibility and reduce inflammation.

**Overall, 11-mercaptoundecanoic acid (MUA) is a versatile molecule with applications in diverse research fields. Its ability to form self-assembled monolayers, its reactivity with gold surfaces, and its potential for functionalization make it a valuable tool for developing new materials, improving existing technologies, and advancing scientific understanding.**

Cross-References

ID SourceID
PubMed CID543502
SCHEMBL ID111144
MeSH IDM0491465

Synonyms (21)

Synonym
11-mercaptoundecanoic acid
11-mercaptoundecanoic acid, 95%
DB08171
11-sulfanylundecanoic acid
71310-21-9
AKOS015893928
STL323763
SCHEMBL111144
undecanoic acid, 11-mercapto-
11-sulfanylundecanoic acid #
FT-0698883
11-mercaptoundecanoic acid, 98%
GS-6888
DTXSID00337585
mfcd00022096
11-mercaptoundecanoicacid
F11363
Q27097399
10-caroboxy-1-decanethiol
A866466
CS-W014785
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (148)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's43 (29.05)29.6817
2010's95 (64.19)24.3611
2020's10 (6.76)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 37.06

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index37.06 (24.57)
Research Supply Index5.03 (2.92)
Research Growth Index4.71 (4.65)
Search Engine Demand Index52.05 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (37.06)

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%
Other152 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]