2-HYDROXY-1,3,5-TRINITROBENZENE, USED IN EXPLOSIVES, AND MATCHES; USED TO PRODUCED COLORED GLASS, LEATHER, AND ELECTRIC BATTERIES; USED AS A REAGENT. Les trois NO 2 sont situés dans les atomes de carbone 2, 4 et 6 du cycle aromatique par rapport à OH. Download sequence data: Biological Unit for 1GVS: monomeric; determined … It is one of the most acidic phenols. Magnify. 0.1 mg/mL in Acetonitrile:Methanol. https://www.britannica.com/science/picric-acid. Masse jaune ou suspension de cristaux humides. The PICRIC ACID molecule shown in the visualization screen can be rotated interactively by keep clicking and moving the mouse button. -Le sel d'ammonium de l'acide picrique a été utilisé comme explosif, il est très puissant mais moins stable que le TNT. Mouse wheel zoom is available as well – the size of the PICRIC ACID molecule can be increased or decreased by scrolling the mouse wheel. Maintain at least a 10% watercontent at all times. Eye contact: Immediately flush with plenty of water. Picric acid. Detailed Hydrocarbon Analysis and SIM DIS, Miscellaneous - Skinner List - Fire Debris, LUFT/LUST (UST) Methods - State Specific - GRH - DRH - TPH, Oil, Grease & TPH - EPA Methods 1664 - 413.2/418.1 and 8440, Wear Metals (Organometallics) and Lubricating Oils, Technical Service - Frequently Asked Questions. The structure data file (SDF/MOL File) of PICRIC ACID is available for download in the SDF page of PICRIC ACID, which provides the information about the atoms, bonds, connectivity and coordinates of PICRIC ACID. Similar Structures: VAST+. L'acide picrique est corrosif en général pour les métaux, à l'exception de l'étain et de l'aluminium. (P340)\nStore in a tightly closed container. In metallurgy a picric acid etch has been commonly used in optical metallography to reveal prior austenite grain boundaries in ferritic steels. 6. D'où la nomenclature UICPA pour ce composé: 2, 4, 6-trinitrophénol (TNP, pour son acronyme en anglais). Storage Condition Storage. A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. Picric acid (from Greek pikros, “bitter”) was so named by the 19th-century French chemist Jean-Baptiste-André Dumas because of the extremely bitter taste of its yellow aqueous solution. Percussion or rapid heating can cause it (or its salts with heavy metals, such as copper, silver, or lead) to explode. De plus, les anneaux ne pourraient pas être alignés les uns sur les autres par une augmentation des répulsions électrostatiques. May explode if dry - keep wet at all times. Our latest podcast episode features popular TED speaker Mara Mintzer. Conversion of complicated chemical-related units is no longer sophisticated with the aid of UnitPot. It was used in medicinal formulations in the treatment of malaria, trichinosis, herpes, smallpox and antiseptics. -En laboratoires cliniques, il est utilisé pour déterminer les taux de créatinine sérique et urinaire. Get medical attention if irritation develops or persists. Structure: B. PHYSICAL AND CHEMICAL PROPERTIES 1. Une autre forme de synthèse consiste à traiter le benzène avec de l'acide nitrique et du nitrate mercurique. The molecular weight of PICRIC ACID is available in molecular weight page of PICRIC ACID, which is calculated as the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element in the molecular formula. Son séchage ou sa déshydratation est dangereux car il augmente les propriétés instables qui le rendent explosif. The contents of this page can freely be shared if cited as follows: Our editors will review what you’ve submitted and determine whether to revise the article. He, S.H. PHENOL TRINITRATE (Skin corrosion/irritation, category 2)\nCauses severe eye irritation. Definition. Certified Reference Material. Sa formule moléculaire est C 6 H 2 (NO 2 ) 3 OH. c1c(cc(c(c1[N+](=O)[O-])O)[N+](=O)[O-])[N+](=O)[O-] Quelles sont les différences entre les plantes angiospermes et gymnospermes? Il est irritant pour la peau et les muqueuses, ne doit pas être ingéré et est toxique pour le corps. À partir de l'acide picrique, certains composés intermédiaires, plusieurs sels de picrate et complexes d'acide picrique sont synthétisés. # M-8330-ADD-3. PICRONITRIC ACID Login to download COA (Lot Number Required). Refer to SDS for detailed product information. The information of the atoms, bonds, connectivity and coordinates included in the chemical structure of PICRIC ACID can easily be identified by this visualization. Below are the list of the other names (synonyms) of PICRIC ACID including the various registry numbers, if available: Visit ChemTopia for further professional chemical information on the basis of a comprehensive intelligence networking platform for experts in the discipline around the globe. 10305 on dry substance, T), Picric acid solution, 100 mug/mL in acetonitrile, PESTANAL(R), analytical standard, Trinitrophenol or picric acid, dry or wetted with <30% water, by mass, Picric acid, wet, with not <10% water [NA1344] [Flammable solid], Picric acid, wet, with not <10% water [NA1344] [Flammable solid], Picric acid solution, ~1.3% in H2O, solution (saturated aqueous), 2-methylbenzo[g][1,3]benzoxazole;2,4,6-trinitrophenol, Trinitrophenol, wetted with not <30% water, by mass, 1-methyl-3,4-dihydro-2H-$b-carboline;picric acid, Picric acid solution, 1.3% in H2O (saturated), Picric acid solution, 0.9-1.1% (alkalimetric), 2-methylbenzo[g][1,3]benzoxazole;picric acid, Trinitrophenol, dry or wetted with < 30% water, by mass, Picric acid, dry or wetted with < 30% water, by mass.