Page last updated: 2024-12-05

1,2-dichloroethylene

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

Description

## 1,2-Dichloroethylene: A Versatile Research Tool

1,2-dichloroethylene (DCE) is a colorless liquid with a sweet, chloroform-like odor. It exists in two isomeric forms: **cis-1,2-dichloroethylene** and **trans-1,2-dichloroethylene**. Both isomers are highly volatile and have applications in various research fields.

**Here's why 1,2-dichloroethylene is important for research:**

**1. Environmental and Industrial Studies:**

* **Groundwater contamination:** DCE is a common contaminant in groundwater due to its industrial use as a solvent and intermediate in chemical production. Research on DCE focuses on its fate and transport in the environment, its degradation by microbes, and the development of remediation technologies.
* **Industrial emissions:** DCE can be released into the atmosphere from industrial processes. Research investigates its atmospheric chemistry, potential for ozone depletion, and its impact on human health.

**2. Medical and Pharmaceutical Research:**

* **Cancer research:** DCE is being studied as a potential therapeutic agent for various cancers due to its ability to induce cell death in cancer cells.
* **Neurological research:** DCE is used as a model compound to study the effects of volatile organic compounds on the nervous system.

**3. Materials Science and Engineering:**

* **Polymer synthesis:** DCE is a valuable precursor in the synthesis of various polymers with specific properties.
* **Nanomaterials research:** DCE plays a role in the fabrication of advanced materials like carbon nanotubes and graphene.

**4. Analytical Chemistry:**

* **Chromatographic analysis:** DCE is used as a solvent in gas chromatography and other analytical techniques for separating and analyzing complex mixtures.

**5. Chemical Reaction Studies:**

* **Organic synthesis:** DCE is a versatile reactant and reagent used in organic synthesis, enabling the development of new compounds and reactions.

**Specific examples of research areas:**

* **Degradation of DCE by microorganisms:** Scientists are studying the potential of using microorganisms to break down DCE in contaminated groundwater.
* **Effect of DCE on the nervous system:** Research aims to understand the mechanisms by which DCE affects brain function and its potential role in neurodegenerative diseases.
* **Synthesis of new polymers using DCE:** Researchers are exploring the use of DCE as a monomer for creating new polymers with enhanced properties for different applications.

In conclusion, 1,2-dichloroethylene is a significant compound in diverse research areas. Its versatility as a solvent, reactant, and model compound makes it a valuable tool for understanding various chemical, biological, and environmental processes. Further research into its properties and applications continues to expand our knowledge and contribute to the advancement of various fields.

1,2-dichloroethylene: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID10900
CHEMBL ID1385560
CHEBI ID18882
MeSH IDM0108465

Synonyms (43)

Synonym
CHEBI:18882 ,
acetylene dichloride
1,2-dichloroethene
1,2-dichloroethylene
NCGC00091531-01
cs & trans 1,2-dichloroethylene
sym-dichloroethylene
einecs 208-750-2
ethylene, 1,2-dichloro-
nci-c56031
brn 1719345
ccris 6227
dichloro-1,2-ethylene [french]
hsdb 149
ethene, 1,2-dichloro-
dioform
1,2-dichloroethylene, all isomers
1,2-dichlor-aethen [german]
ethene, 1,2-dichloro-, (1z)-
540-59-0
cis & trans 1,2-dichloroethylene
cis,trans-1,2-dichloroethylene
FT-0696065
FT-0690818
dtxsid8024991 ,
dichloro-1,2-ethylene
xu9rua6yut ,
2-01-00-00158 (beilstein handbook reference)
1,2-dichlor-aethen
unii-xu9rua6yut
FT-0604919
AKOS025243626
chlorovinyl chloride
1,2-dichloroethene #
1,2-dichloroethylene (cis & trans)
1,2-dichloroethylene,c&t
CHEMBL1385560
cis-/trans-1,2-dichloroethene
ethylene, 1,2-dichloro- (8ci); 1,2-dichloroethene; 1,2-dichloroethylene; acetylene dichloride; dioform; sym-dichloroethylene
Q161475
1,2-dichlora currencythylen
1,2-dichloroethylene (mixture of cis and trans)
AT37401

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Therefore, t-DCE is not considered to be uniquely toxic to the rat conceptus."( Developmental toxicity of inhaled trans-1,2-dichloroethylene in the rat.
Alvarez, L; Hurtt, ME; Valentine, R, 1993
)
0.55

Pharmacokinetics

ExcerptReferenceRelevance
" Interactions between chemicals may involve pharmacokinetic and/or pharmacodynamic effects resulting in modulation of toxicity."( Chloroethylene mixtures: pharmacokinetic modeling and in vitro metabolism of vinyl chloride, trichloroethylene, and trans-1,2-dichloroethylene in rat.
Barton, HA; Creech, JR; Godin, CS; Randall, GM; Seckel, CS, 1995
)
0.5

Dosage Studied

ExcerptRelevanceReference
" Hepatic microsomes were prepared from groups of rats prior to dosing and at 2, 5, 12, and 24 hr postdosing with DCE (100 mg/kg ip), and total P450 content and the activity of CYP2E1 was determined."( Do endogenous volatile organic chemicals measured in breath reflect and maintain CYP2E1 levels in vivo?
Bucher, JR; Etheridge, AS; Mathews, JM; Raymer, JH; Velez, GR, 1997
)
0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
chloroethenesA chloroalkene that is ethene in which one or more of the hydrogens has been replaced by chlorine.
[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]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency1.12200.003245.467312,589.2998AID2517
Chain A, TYROSYL-DNA PHOSPHODIESTERASEHomo sapiens (human)Potency89.12510.004023.8416100.0000AID485290
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency3.16230.000214.376460.0339AID588533
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (131)

TimeframeStudies, This Drug (%)All Drugs %
pre-199012 (9.16)18.7374
1990's13 (9.92)18.2507
2000's50 (38.17)29.6817
2010's51 (38.93)24.3611
2020's5 (3.82)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 56.38

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

MetricThis Compound (vs All)
Research Demand Index56.38 (24.57)
Research Supply Index4.92 (2.92)
Research Growth Index4.92 (4.65)
Search Engine Demand Index90.43 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (56.38)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews4 (2.94%)6.00%
Case Studies1 (0.74%)4.05%
Observational0 (0.00%)0.25%
Other131 (96.32%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]