Tetranitromethane (BioCAD00000018409)

blood

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)

Reviewed

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.

Entity Information

DBLinks

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

Metabolic Network
ID EC Number Name
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Organism Source

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
View All Pathways