Page last updated: 2024-12-06

tetraphenylarsonium

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

Description

Tetraphenylarsonium is a large, lipophilic cation with a tetrahedral structure. It is commonly used as a counterion in the synthesis of various organic and inorganic compounds. This compound is often employed to form salts of anionic species, which can be helpful for isolating and characterizing these species. Tetraphenylarsonium is known for its ability to act as a phase-transfer catalyst in certain reactions, facilitating the transfer of reagents between different phases. Due to its lipophilic nature, it is often used in studies involving membrane transport and ion channels. The compound is generally synthesized through reactions of phenyllithium with arsenic trichloride, followed by subsequent purification techniques. Research involving tetraphenylarsonium is driven by its wide range of applications in various scientific disciplines, including organic chemistry, inorganic chemistry, and biochemistry.'

tetraphenylarsonium: RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

tetraphenylarsonium : An arsonium ion consisting of four phenyl groups attached to a central arsonium. [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 CID68178
CHEBI ID9501
MeSH IDM0054144

Synonyms (12)

Synonym
tetraphenylarsanium
[asph4](+)
asph4(+)
CHEBI:9501
tetraphenyl-arsonium
tetraphenylarsenic(1+)
tetraphenylarsonium
pjmjfvqkdbrmip-uhfffaoysa-
inchi=1/c24h20as/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20h/q+1
tetra(phenyl)arsanium
Q27108414
DTXSID10862070
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
arsonium ionArsonium, AsH4(+), and derivatives formed by substitution by univalent groups.
[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 (24)

TimeframeStudies, This Drug (%)All Drugs %
pre-199015 (62.50)18.7374
1990's7 (29.17)18.2507
2000's1 (4.17)29.6817
2010's1 (4.17)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.60

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

MetricThis Compound (vs All)
Research Demand Index27.60 (24.57)
Research Supply Index3.26 (2.92)
Research Growth Index4.24 (4.65)
Search Engine Demand Index22.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.60)

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%
Other25 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]