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Tetranitromethane

Catalog No. T25003 Name Sigma Aldrich
CAS Number 509-14-8 Website http://www.sigmaaldrich.com
M. F. CN4O8 Telephone 1-800-521-8956
M. W. 196.0327 Fax
Purity Email
Storage Chembase ID: 129808

SYNONYMS

Title
四硝基甲烷
IUPAC name
tetranitromethane
IUPAC Traditional name
tetranitromethane
Synonyms
NSC 16146
TNM

DATABASE IDS

CAS Number 509-14-8
EC Number 208-094-7
MDL Number MFCD00007391
PubChem SID 24900040

PROPERTIES

Linear Formula C(NO2)4
Boiling Point 126 °C(lit.)
Density 1.637 g/mL at 25 °C(lit.)
Flash Point 113 °C
Flash Point 235.4 °F
Melting Point 13-14 °C(lit.)
Refractive Index n20/D 1.438(lit.)
Vapor Pressure 8.4 mmHg ( 20 °C)
GHS Pictograms GHS03
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H271-H301-H315-H319-H330-H335-H351
European Hazard Symbols Oxidising Oxidising (O)
European Hazard Symbols Highly toxic Highly toxic (T+)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P220-P260-P281-P284-P301 + P310-P305 + P351 + P338
RID/ADR UN 1510 5.1/PG 1
Risk Statements 8-25-26-36/37/38-40
RTECS PB4025000
Safety Statements 17-28-36/37-45
Storage Temperature 2-8°C
Hazard Class 5.1
UN Number 1510
Packing Group 1
German water hazard class 3

DETAILS

Description (English)
Application
Reagent for nitration of enol silyl ethers7 and aromatic compounds.8 Employed in the photooxidation of sulfides to sulfoxides.9
Reactant involved in:
• Nitration of electrophilic alkenes1
• Reactions with B-alkylcatecholboranes forming oxime ethers2
• Heterocyclization of electrophilic alkenes3
• Ring opening of aziridines4
• Acts as an electron acceptor in the mechanism of aerobic visible light formic acid oxidation5
• Reactions with vinyl ketones6
Packaging
1, 5 g in glass bottle
Description (简体中文)
Application
烯醇硅醚7和芳香族化合物的硝化试剂。8用于硫化物到亚砜的光氧化反应。9
Reactant involved in:
• Nitration of electrophilic alkenes1
• Reactions with B-alkylcatecholboranes forming oxime ethers2
• Heterocyclization of electrophilic alkenes3
• Ring opening of aziridines4
• Acts as an electron acceptor in the mechanism of aerobic visible light formic acid oxidation5
• Reactions with vinyl ketones6
包装
1, 5 g in glass bottle

REFERENCES