Page last updated: 2024-12-06

1-octanesulfonic acid

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

Description

1-Octanesulfonic acid is an organic compound with the formula CH3(CH2)7SO3H. It is a colorless, oily liquid that is soluble in water. It is a strong acid and is used in a variety of industrial applications. The compound has various applications, including as a surfactant, emulsifier, and dispersant. Its strong acidic properties make it a useful catalyst in various organic reactions. Its importance stems from its ability to form stable salts with a wide range of cations, rendering it useful in various industries. Notably, 1-octanesulfonic acid is used in the production of petroleum sulfonates, which are important additives in drilling fluids and lubricating oils. It also finds application in the synthesis of pharmaceuticals and agrochemicals. It is studied for its potential applications in diverse areas, such as pharmaceuticals, cosmetics, and industrial cleaning agents. The research on this compound primarily focuses on developing new and efficient methods for its synthesis, exploring its potential as a catalyst in organic reactions, and investigating its environmental impact.'

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

Cross-References

ID SourceID
PubMed CID49939
CHEMBL ID1208308
CHEBI ID39422
SCHEMBL ID36542
MeSH IDM0124309

Synonyms (28)

Synonym
einecs 223-535-3
octanesulphonic acid
unii-du4821i15a
du4821i15a ,
sodium octylsulfonate
octane-1-sulfonic acid
nsc2738
nsc23385
1-octanesulfonic acid
3944-72-7
CHEBI:39422 ,
FT-0695297
octanesulfonic acid
CHEMBL1208308
AKOS006230663
SCHEMBL36542
n-octanesulfonic acid
octylsulfonic acid
n-octane sulfonic acid
octane-1-sulphonic acid
WLGDAKIJYPIYLR-UHFFFAOYSA-N
1-octane sulfonic acid
DTXSID5041277
Q27119858
SB37003
octane-1-sulfonicacid
CS-0452055
EN300-1270681

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Drug safety assessment studies including acute toxicity, hemolysis test, intravenous stimulation and injection anaphylaxis revealed that the PTX-M was safe for intravenous injection."( Pharmacokinetics, biodistribution, efficacy and safety of N-octyl-O-sulfate chitosan micelles loaded with paclitaxel.
Ding, Q; Guo, Q; Ping, Q; Qu, G; Shen, Z; Sun, Y; Wu, X; Yao, Z; Yuan, S; Zhang, C; Zhou, H, 2008
)
0.35
" Oxidative toxicity has been suggested to be one of the major toxic pathways for PFCs to induce adverse effects on organisms."( Oxidative toxicity of perfluorinated chemicals in green mussel and bioaccumulation factor dependent quantitative structure-activity relationship.
Chang, VW; Gin, KY; Liu, C, 2014
)
0.4

Compound-Compound Interactions

ExcerptReferenceRelevance
"A hollow fiber-based liquid phase microextraction strategy combined with high-performance liquid chromatography was evaluated for the quantitative determination of trimetazidine in human plasma."( Hollow fiber-based liquid membrane microextraction combined with high-performance liquid chromatography for extraction and determination of trimetazidine in human plasma.
Bi, K; Chen, X; Liu, D; Lv, J; Ye, J; Zhao, X, 2013
)
0.39

Bioavailability

ExcerptReferenceRelevance
" These results clearly showed that PTX-M had the similar antitumor efficacy as Taxol, but significantly reduced the toxicity and improved the bioavailability of PTX."( Pharmacokinetics, biodistribution, efficacy and safety of N-octyl-O-sulfate chitosan micelles loaded with paclitaxel.
Ding, Q; Guo, Q; Ping, Q; Qu, G; Shen, Z; Sun, Y; Wu, X; Yao, Z; Yuan, S; Zhang, C; Zhou, H, 2008
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
local anaestheticAny member of a group of drugs that reversibly inhibit the propagation of signals along nerves. Wide variations in potency, stability, toxicity, water-solubility and duration of action determine the route used for administration, e.g. topical, intravenous, epidural or spinal block.
[role 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]

Drug Classes (1)

ClassDescription
organosulfonic acidAn organic derivative of sulfonic acid in which the sulfo group is linked directly to carbon.
[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 (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (14.71)18.7374
1990's2 (5.88)18.2507
2000's11 (32.35)29.6817
2010's14 (41.18)24.3611
2020's2 (5.88)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 46.40

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 Index46.40 (24.57)
Research Supply Index3.58 (2.92)
Research Growth Index5.11 (4.65)
Search Engine Demand Index66.16 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (46.40)

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%
Other35 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]