| Weight | 245.103 g/mol |
|---|---|
| Formula | C6H3N3O8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Styphnic acid (82-71-3)
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- First-Principles Study of Electronic, Absorption, and Thermodynamic Properties of Crystalline Styphnic Acid and Its Metal Salts (Journal of Physical Chemistry B, 2009)
- Synthesis, structural investigation and thermal analyses of a novel coordination compound [Cd(DAT)6](HTNR)23.5H2O (DAT = 1,5-diaminotetrazole, H2TNR = styphnic acid) (Journal of Molecular Structure, 2008)
- Thermochemistry of nitroresorcinols. i. 2,4,6-trinitroresorcinol (styphnic acid) (Thermochimica Acta, 1990)
- Manufacture of styphnic acid (1940)
- Process for the decomposition of styphnic acid (1946)
- Adsorption of styphnic acid on activated carbon (Indian Journal of Chemical Technology, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H201: Explosive; mass explosion hazard
Danger Explosives - Div 1.1 - H312: Harmful in contact with skin
Warning Acute toxicity, dermal - Category 4 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 -
SMILESC1=C(C(=C(C(=C1[N+](=O)[O-])O)[N+](=O)[O-])O)[N+](=O)[O-]
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InChIKeyIXHMHWIBCIYOAZ-UHFFFAOYSA-N
- Pubchem - Styphnic acid
- Wikipedia - styphnic acid
Styphnic acid (from Greek stryphnos "astringent"), or 2,4,6-trinitro-1,3-benzenediol, is a yellow astringent acid that forms hexagonal crystals. It is used in the manufacture of dyes, pigments, inks, medicines, and explosives such as lead styphnate. It is itself a low sensitivity explosive, similar to picric acid, but explodes upon rapid heating.
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