| Weight | 439.209 g/mol |
|---|---|
| Formula | C12H5N7O12 |
| Hydrogen Acceptors | 13 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 8 |
Dipicrylamine (131-73-7)
dipicrylaminate · 2,4,6,2',4',6'-hexanitrodiphenylamine · dipicrylamine potassium salt
Score:
#1019 in Physics
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#2899 in Chemistry
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- Transport kinetics of dipicrylamine through lipid bilayer membranes. Effects of membrane structure (Biochimica et Biophysica Acta, 1977)
- Attractive Inter- and Intramolecular N.cntdot..cntdot..cntdot.O Interactions in N,N-Dipicrylamine and Its Ionic Complexes (The Journal of Physical Chemistry, 1994)
- Dipicrylamine transport across an ultrathin phosphatidylethanolamine membrane (Journal of Electroanalytical Chemistry, 1975)
- ELECTROROTATION OF ERYTHROCYTES TREATED WITH DIPICRYLAMINE : MOBILE CHARGES WITHIN THE MEMBRANE SHOW THEIR SIGNATURE IN ROTATIONAL SPECTRA (The Journal of Membrane Biology, 1996)
- Extractive-spectrophotometric determination of some phenothiazines with dipicrylamine and picric acid. (Journal of Pharmaceutical and Biomedical Analysis, 2002)
- Charge density studies of weak interactions in dipicrylamine (Journal of Physical Chemistry A, 2002)
-
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 - H310: Fatal in contact with skin
Danger Acute toxicity, dermal - Category 1, 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - dipicrylaminate
- 2,4,6,2',4',6'-hexanitrodiphenylamine
- dipicrylamine potassium salt
-
SMILESC1=C(C=C(C(=C1[N+](=O)[O-])NC2=C(C=C(C=C2[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
-
InChIKeyCBCIHIVRDWLAME-UHFFFAOYSA-N
- Pubchem - Dipicrylamine
- Wikipedia - dipicrylamine
Hexanitrodiphenylamine (abbreviated HND), is an explosive chemical compound with the formula C12H5N7O12. HND was used extensively by the Japanese during World War II but was discontinued due to its toxicity.
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