1,2-Dibromoethane (BioCAD00000001546)
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Metabolite Card
Formula: C2H4Br2 (185.868)
SMILES: BrCCBr
Synonyms [en]
1,2-Dibromoethane; Ethylene Dibromide; sym-Dibromoethane; Ethylene Bromide; alpha,omega-Dibromoethane; EDB
Last reviewed on 2024-06-28.
Cite this Page
1,2-Dibromoethane. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000001546). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
1,2-Dibromoethane, also known as ethylene dibromide or DBE, belongs to the class of organic compounds known as organobromides. Organobromides are compounds containing a chemical bond between a carbon atom and a bromine atom. 1,2-Dibromoethane is possibly neutral. Trace amounts of 1,2-dibromoethane occur naturally in the ocean, where it is formed probably by algae and kelp. 1,2-Dibromoethane is formally rated as a probable carcinogen (by IARC 2A) and is also a potentially toxic compound. Breathing high levels may cause depression and collapse. 1,2-Dibromoethane is rapidly absorbed by ingestion, inhalation, and dermal routes, then distributed mainly to the kidneys, liver, and spleen. It can be metabolized by either the cytochrome P-450 system or the glutathione S-transferase system. These metabolites may be further broken down and excreted in the urine. The metabolite 2-bromoacetaldehyde produces liver damage by binding to cellular proteins. Long term exposure can result in liver, kidney, and reproductive system damage. 1,2-Dibromoethane is also known to have adverse effects on the brain. S-(2-bromoethyl)glutathione, another metabolite, exerts genotoxic and carcinogenic effects by binding to DNA.
DBLinks
- CAS Registry Number: 106-93-4
- PubChem CID: 7839
- ChEBI: 28534
- HMDB: HMDB0060334
- LipidMaps:
- KEGG: C11088
- BioCyc: 12-DIBROMOETHANE
- NCBI MeSH: Ethylene Dibromide
- Wikipedia: 1,2-Dibromoethane
Other DBLinks
- CAS Registry Number: 106-93-4
- CAS Registry Number: 25620-62-6
- CAS Registry Number: 557-91-5
- CAS Registry Number: 57260-71-6
- PubChem: 11201
- PubChem: 7839
- ChEBI: ChEBI:28534
- HMDB: HMDB0060334
- KEGG: C11088
- BioCyc: 12-DIBROMOETHANE
- NCBI MeSH: Ethylene Dibromide
- Wikipedia: 1,1-Dibromoethane
- Wikipedia: 1,2-Dibromoethane
- Wikipedia: 1\,2-Dibromoethane
- MoNA: HMDB0060334_c_ms_102428
- MoNA: HMDB0060334_c_ms_102429
- MoNA: JP004909
- MoNA: JP007661
- Metlin: METLIN_68830
- Coconut NaturalProduct: CNP0327546.0
- Coconut NaturalProduct: CNP0495552.0
- Coconut NaturalProduct: CNP0591557.0
Class / Ontology
- WishartLab ClassyFire: [Organobromides] Organobromides
- ChEBI: [CHEBI:28534] 1,2-dibromoethane
- Coconut NaturalProduct: [Piperidine alkaloids] Piperidine alkaloids
- Coconut NaturalProduct: [Halogenated hydrocarbons] Halogenated hydrocarbons
| ID | EC Number | Name |
|---|---|---|
| KEGG:R07112 | 1.14.14.- | 1,2-dibromoethane,NADPH:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing) |
| KEGG:R07113 | 2.5.1.18 | 1,2-dibromoethane:glutathione ethylenetransferase (episulfonium-forming) |