Page last updated: 2024-12-05

1,6-hexanedithiol

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

Description

1,6-Hexanedithiol is a bifunctional thiol compound. It is a colorless liquid with a strong odor. It is commonly synthesized by the reaction of 1,6-dibromohexane with sodium hydrosulfide in ethanol. 1,6-Hexanedithiol has a variety of applications, including as a cross-linking agent for polymers, a building block for organic synthesis, and a component of biocompatible materials. It is also being studied for its potential applications in the development of new drugs and therapies.'
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1,6-hexanedithiol: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID14491
CHEBI ID173638
SCHEMBL ID64527
MeSH IDM0486199

Synonyms (43)

Synonym
CHEBI:173638
nsc-29031
usaf uctl-72
1,6-hexanedithiol
1,6-hexanedimercaptan
wln: sh6sh
1,6-dimercaptohexane
nsc29031
1191-43-1
brn 1732507
hexamethylene dimercaptan
fema no. 3495
ndr-139
einecs 214-735-1
nsc 29031
hexane-1,6-dithiol
1,6-hexamethylenedithiol
1,6-hexanedithiol, >=97%, fg
1,6-hexanedithiol, 96%
inchi=1/c6h14s2/c7-5-3-1-2-4-6-8/h7-8h,1-6h2
srzxcowfgpicga-uhfffaoysa-
H0334
A804205
unii-rwn7rm884e
1,6-hexane dithiol
rwn7rm884e ,
4-01-00-02559 (beilstein handbook reference)
FT-0607015
AKOS015897443
1,6-hexanedithiol [fhfi]
1,6- dimercaptohexane
SCHEMBL64527
Q-100088
hexanedithiol-(1,6)
DTXSID60152317
mfcd00004910
1,6-hexanedithiol, 99.5%
hexamethylendithiol
fema 3495
1, 6-hexanedimercaptan
Q27288323
D90840
AS-57326
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
alkanethiolAn alkanethiol is a compound in which a sulfanyl group, -SH, is attached to an alkyl group.
[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-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's8 (33.33)29.6817
2010's16 (66.67)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: 27.24

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 Index27.24 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index31.58 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.24)

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%
Other24 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]