Metabolite Card
Formula: CHCl3 (117.9144)
SMILES: ClC(Cl)Cl
Synonyms [en]
Chloroform; Trichloromethane; Formyl trichloride; Chloroforme; methane trichloride; Methenyl trichloride
Last reviewed on 2024-06-28.
Cite this Page
Chloroform. 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: BioCAD00000008366). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Chloroform is found in spearmint. Indirect food additive arising from adhesives and polymers Chloroform is a common solvent in the laboratory because it is relatively unreactive, miscible with most organic liquids, and conveniently volatile. Chloroform is used as a solvent in the pharmaceutical industry and for producing dyes and pesticides. Chloroform is an effective solvent for alkaloids in their base form and thus plant material is commonly extracted with chloroform for pharmaceutical processing. For example, it is commercially used to extract morphine from poppies and scopolamine from Datura plants. Chloroform containing deuterium (heavy hydrogen), CDCl3, is a common solvent used in NMR spectroscopy. It can be used to bond pieces of acrylic glass (also known under the trade names Perspex and Plexiglas). Chloroform is a solvent of phenol:chloroform:isoamyl alcohol 25:24:1 is used to dissolve non-nucleic acid biomolecules in DNA and RNA extractions. Chloroform is the organic compound with formula CHCl3. It does not undergo combustion in air, although it will burn when mixed with more flammable substances. It is a member of a group of compounds known as trihalomethanes. Chloroform has myriad uses as a reagent and a solvent. It is also considered an environmental hazard. Several million tons are produced annually. The output of this process is a mixture of the four chloromethanes: chloromethane, dichloromethane, chloroform (trichloromethane), and carbon tetrachloride, which are then separated by distillation. The total global flux of chloroform through the environment is approximately 660000 tonnes per year, and about 90% of emissions are natural in origin. Many kinds of seaweed produce chloroform, and fungi are believed to produce chloroform in soil. Abiotic process is also believed to contribute to natural chloroform productions in soils although the mechanism is still unclear. Chloroform volatilizes readily from soil and surface water and undergoes degradation in air to produce phosgene, dichloromethane, formyl chloride, carbon monoxide, carbon dioxide, and hydrogen chloride. Its half-life in air ranges from 55 to 620 days. Biodegradation in water and soil is slow. Chloroform does not significantly bioaccumulate in aquatic organisms.
DBLinks
- CAS Registry Number: 67-66-3
- PubChem CID: 6212
- ChEBI: 35255
- HMDB: HMDB0029596
- LipidMaps:
- KEGG: C13827
- BioCyc: CPD-843
- NCBI MeSH: Chloroform
- Wikipedia: Chloroform
Other DBLinks
- CAS Registry Number: 3170-80-7
- CAS Registry Number: 67-66-3
- PubChem: 6212
- ChEBI: ChEBI:35255
- HMDB: HMDB0029596
- KEGG: C13827
- BioCyc: CPD-843
- NCBI MeSH: Chloroform
- Wikipedia: Chloroform
- DrugBank: DB11387
- RefMet: RM0161187
- MoNA: HMDB0029596_c_ms_100343
- MoNA: HMDB0029596_c_ms_100344
- MoNA: HMDB0029596_c_ms_100345
- MoNA: JP000937
- MoNA: JP002105
- MoNA: JP002340
- Metlin: METLIN_69721
- Coconut NaturalProduct: CNP0479643.0
Class / Ontology
- WishartLab ClassyFire: [Halomethanes] Halomethanes
- RefMet: [Trihalomethanes] Trihalomethanes
- ChEBI: [CHEBI:35255] chloroform
- Coconut NaturalProduct: [Halogenated hydrocarbons] Halogenated hydrocarbons
| ID | EC Number | Name |
|---|---|---|
| BioCyc:R525-RXN | 1.14.15.- | CPD-842 + 6 Reduced-Putidaredoxins + 5 PROTON + OXYGEN-MOLECULE --> CPD-843 + CL- + 6 Oxidized-Putidaredoxins + 2 WATER |
| BioCyc:R526-RXN | CPD-843 + Donor-H2 --> CPD-681 + CL- + Acceptor + PROTON | |
| BioCyc:RXN-8402 | 2 CPD-8214 + Donor-H2<=>2 CPD-843 + Acceptor |