Page last updated: 2024-11-06

ethylenesulfonic acid

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

Ethylenesulfonic acid (ESA) is a colorless, hygroscopic, strong organic acid with the formula CH2(SO3H)CH2OH. It is a versatile chemical intermediate used in various applications, including the production of surfactants, resins, and polymers. ESA is typically synthesized by reacting ethylene oxide with sulfur trioxide in the presence of a catalyst. Its strong acidic nature makes it an effective catalyst in organic reactions, such as esterification and alkylation. ESA is also used as a plasticizer in the production of polymers, enhancing their flexibility and processability. The biological effects of ESA are not well-studied, but it is generally considered to be a relatively safe compound. ESA's importance stems from its wide range of applications in various industries, and its properties make it a valuable chemical intermediate. Research on ESA focuses on developing new synthetic methods, exploring its potential applications in various fields, and investigating its environmental impact.'

Cross-References

ID SourceID
PubMed CID62474
CHEMBL ID1236690
SCHEMBL ID16079
MeSH IDM0227449

Synonyms (31)

Synonym
V0134
CHEMBL1236690
1184-84-5
ethylenesulfonic acid
ethenesulfonic acid
nsc8957
VSO ,
vinylsulphonic acid
vinylsulfonic acid
1RQL ,
DB04359
AKOS006230508
unii-gj6489r1we
ethylenesulphonic acid
gj6489r1we ,
einecs 214-676-1
vsa-s
vsa-h
SCHEMBL16079
NLVXSWCKKBEXTG-UHFFFAOYSA-N
ethylene sulfonic acid
vinyl sulfonic acid
DTXSID2047018
vinylsulfonic acid, >/=97%
T71619
FT-0722512
sodium ethenesulfonate(25%nasalt)
Q2527228
mfcd09743544
ethylenesulfonicacid
BS-44145
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain B, Phosphonoacetaldehyde HydrolaseBacillus cereusKi1,790.00001,790.00001,790.00001,790.0000AID977610
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID977610Experimentally measured binding affinity data (Ki) for protein-ligand complexes derived from PDB2004The Journal of biological chemistry, Mar-05, Volume: 279, Issue:10
X-ray crystallographic and site-directed mutagenesis analysis of the mechanism of Schiff-base formation in phosphonoacetaldehyde hydrolase catalysis.
AID1811Experimentally measured binding affinity data derived from PDB2004The Journal of biological chemistry, Mar-05, Volume: 279, Issue:10
X-ray crystallographic and site-directed mutagenesis analysis of the mechanism of Schiff-base formation in phosphonoacetaldehyde hydrolase catalysis.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (16)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (6.25)18.7374
1990's1 (6.25)18.2507
2000's8 (50.00)29.6817
2010's6 (37.50)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: 12.48

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 Index12.48 (24.57)
Research Supply Index2.83 (2.92)
Research Growth Index5.32 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.48)

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%
Other16 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]