Tetranitromethane (BioCAD00000018409)
Metabolite Card
Formula: CN4O8 (195.9716)
SMILES: O=N(=O)C(N(=O)=O)(N(=O)=O)N(=O)=O
Synonyms [en]
Tetranitromethane; WLN: WNXNWNWNW; Tetan; TETRANITROMETHANE [HSDB]; Methane, tetranitro-; Tetranitromethane(Technical)
Last reviewed on 2024-06-28.
Cite this Page
Tetranitromethane. 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: BioCAD00000018409). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Tetranitromethane appears as a pale yellow liquid. Irritates skin and respiratory tract. Very toxic by inhalation. Difficult to ignite. Burns at a steady rate once ignited. Under prolonged exposure to fire or heat containers may rupture violently and rocket Produces toxic oxides of nitrogen during combustion. Tetranitromethane is an organonitrogen compound. Tetranitromethane is a synthetic, oily, colorless to pale yellow liquid that is insoluble in water and soluble in alcohol and ether. Tetranitromethane is used as an oxidizing agent in rocket propellants and explosives as well as an additive to increase the cetane number of diesel fuel. In science, it is used as both an analytical reagent for the detection of double bonds in organic compounds and as a mild nitrating reagent that reacts with tyrosine residues in proteins. The primary route of potential human exposure to tetranitromethane is inhalation. Acute inhalation exposure to tetranitromethane can result in irritation of the respiratory tract, buildup of fluid in the lungs (pulmonary edema) and interference with the oxygen-carrying capacity of red blood cells (methemoglobinemia). Contact with this compound can cause irritation of the eyes and skin. It is reasonably anticipated to be a human carcinogen. (NCI05) Tetranitromethane can cause cancer according to The National Toxicology Program. Corrosive oxidant, explosive; additive to diesel and rocket fuels; causes skin and lung irritation; proposed war gas. A useful reagent for studying the modification of specific amino acids, particularly tyrosine residues in proteins. Has also been used for studying carbanion formation and for detecting the presence of double bonds in organic compounds.
DBLinks
- CAS Registry Number: 509-14-8
- PubChem CID: 10509
- ChEBI: 82372
- HMDB: HMDB0258923
- LipidMaps:
- KEGG: C19300
- BioCyc: TETRANITROMETHANE
- NCBI MeSH: Tetranitromethane
- Wikipedia: Tetranitromethane
Other DBLinks
- CAS Registry Number: 509-14-8
- PubChem: 10509
- ChEBI: ChEBI:82372
- HMDB: HMDB0258923
- KEGG: C19300
- BioCyc: TETRANITROMETHANE
- NCBI MeSH: Tetranitromethane
- Wikipedia: Tetranitromethane
- Metlin: METLIN_73012
Class / Ontology
- WishartLab ClassyFire: [Ortho amides] Ortho amides
- ChEBI: [CHEBI:82372] Tetranitromethane
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:META_PWY-6628 | superpathway of L-phenylalanine biosynthesis |
| BioCyc:META_PHESYN | L-phenylalanine biosynthesis I |
| BioCyc:META_PWY-5028 | L-histidine degradation II |
| BioCyc:META_ALL-CHORISMATE-PWY | superpathway of chorismate metabolism |
| BioCyc:ECO_COMPLETE-ARO-PWY | superpathway of aromatic amino acid biosynthesis |
| BioCyc:META_PWY-7140 | myricetin gentiobioside biosynthesis |
| BioCyc:META_PWY-7143 | kaempferol gentiobioside biosynthesis |
| BioCyc:META_COMPLETE-ARO-PWY | superpathway of aromatic amino acid biosynthesis |
| BioCyc:META_PWY-7137 | quercetin gentiotetraside biosynthesis |
| BioCyc:ECO_ALL-CHORISMATE-PWY | superpathway of chorismate metabolism |
| BioCyc:ECO_PHESYN | L-phenylalanine biosynthesis I |
| PlantCyc:PLANT_PWY-6360 | flavonol glucosylation I |
| PlantCyc:PLANT_PWY-7137 | quercetin gentiotetraside biosynthesis |
| PlantCyc:PLANT_PWY-7140 | myricetin gentiobioside biosynthesis |
| PlantCyc:PLANT_PWY-7143 | kaempferol gentiobioside biosynthesis |