Identification | More | [Name]
3-NITROBENZAMIDE | [CAS]
645-09-0 | [Synonyms]
3-NITROBENZAMIDE M-NITROBENZAMIDE 3-nitro-benzamid Benzamide, m-nitro- m-nitro-benzamid 3-Nitrobenzamide,98% | [EINECS(EC#)]
211-431-0 | [Molecular Formula]
C7H6N2O3 | [MDL Number]
MFCD00007984 | [Molecular Weight]
166.13 | [MOL File]
645-09-0.mol |
Chemical Properties | Back Directory | [Appearance]
yellow powder | [Melting point ]
140-143 °C (lit.) | [Boiling point ]
312.55°C | [density ]
1.4994 (rough estimate) | [refractive index ]
1.5880 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Crystalline Powder or Crystals | [pka]
14.86±0.50(Predicted) | [color ]
Yellow | [Stability:]
Stable. Combustible. Incompatible with strong oxidizing agents. | [BRN ]
777185 | [CAS DataBase Reference]
645-09-0(CAS DataBase Reference) | [EPA Substance Registry System]
m-Nitrobenzamide (645-09-0) |
Safety Data | Back Directory | [Risk Statements ]
R22:Harmful if swallowed. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
CV5601250
| [TSCA ]
Yes | [HS Code ]
29242990 |
Hazard Information | Back Directory | [General Description]
Yellow powder. | [Reactivity Profile]
A nitrated amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
Flash point data for this compound are not available, however, M-NITROBENZAMIDE is probably combustible. | [Chemical Properties]
yellow powder |
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