| Weight | 196.031 g/mol |
|---|---|
| Formula | CN4O8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
TETRANITROMETHANE (509-14-8)
Score:
#183 in Biochemistry
,
#284 in Physics
,
#818 in Chemistry
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- Sigma-Aldrich - TETRANITROMETHANE47.90 - 160.50 USD
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- Tetranitromethane. A reagent for the nitration of tyrosyl residues in proteins. (Biochemistry, 1966)
- Pattern of hydroxyl radical addition to uracil and methyl- and carboxyl-substituted uracils. Electron transfer of hydroxyl adducts with N,N,N',N'-tetramethyl-p-phenylenediamine and tetranitromethane (Journal of the American Chemical Society, 1981)
- Environmentally sensitive tyrosyl residues. Nitration with tetranitromethane. (Biochemistry, 1967)
- [44] Nitration with tetranitromethane (Methods in Enzymology, 1972)
- THE PULSE RADIOLYSIS OF AQUEOUS TETRANITROMETHANE. I. RATE CONSTANTS AND THE EXTINCTION COEFFICIENT OF e$sup -$aq. II. OXYGENATED SOLUTIONS (The Journal of Physical Chemistry, 1965)
- Tetranitromethane. A Reagent for the Nitration of Tyrosine and Tyrosyl Residues of Proteins1 (Journal of the American Chemical Society, 1966)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H271: May cause fire or explosion; strong Oxidizer
Danger Oxidizing liquids; Oxidizing solids - Category 1 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H335: May cause respiratory irritation
Warning Specific target organ toxicity, single exposure; Respiratory tract irritation - Category 3 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 -
SMILESC([N+](=O)[O-])([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-]
-
InChIKeyNYTOUQBROMCLBJ-UHFFFAOYSA-N
- Pubchem - TETRANITROMETHANE
- Wikipedia - tetranitromethane
Tetranitromethane or TNM is an organic oxidizer with chemical formula C(NO2)4. Its chemical structure consists of four nitro groups attached to one carbon atom. In 1857 it was first synthesised by the reaction of sodium cyanoacetamide with nitric acid.
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TETRANITROMETHANE
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