BENZONITRILE LR FOR SYNTHESIS Phenyl Cyanide
BENZONITRILE LR FOR SYNTHESIS Phenyl Cyanide
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| Standard packing | 0.00 Box |
|---|---|
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<strong style="text-align: justify;"><span style="color: rgb(32, 33, 34); font-family: sans-serif; font-size: 14px;">Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis.</span></strong></p>
<p>
<strong><span style="font-weight: bold; color: rgb(95, 99, 104); font-family: arial, sans-serif;">Benzonitrile</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> is used as a solvent and chemical intermediate for the </span><span style="font-weight: bold; color: rgb(95, 99, 104); font-family: arial, sans-serif;">synthesis</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> of pharmaceuticals, dyestuffs and rubber chemicals through the </span><span style="font-weight: bold; color: rgb(95, 99, 104); font-family: arial, sans-serif;">reactions.</span></strong></p>
<table border="1" cellpadding="1" cellspacing="1">
<tbody>
<tr>
<td>
Physical state at 20 °C : </td>
<td>
Liquid.</td>
</tr>
<tr>
<td>
Odour : </td>
<td>
Strong, vinegar-like</td>
</tr>
<tr>
<td>
Odour threshold : </td>
<td>
No data available.</td>
</tr>
<tr>
<td>
pH value :</td>
<td>
No data available.</td>
</tr>
<tr>
<td>
Melting point [°C] : </td>
<td>
16.2 °C</td>
</tr>
<tr>
<td>
Decomposition point [°C] : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Critical temperature [°C] :</td>
<td>
N/A</td>
</tr>
<tr>
<td>
Auto-ignition temperature [°C] : </td>
<td>
485 °C</td>
</tr>
<tr>
<td>
Flammability (solid, gas) : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Flammable liquid and vapour</td>
<td>
</td>
</tr>
<tr>
<td>
Flash point [°C] : </td>
<td>
40°C</td>
</tr>
<tr>
<td>
Boiling point [°C] : </td>
<td>
117 - 118 °C</td>
</tr>
<tr>
<td>
Initial boiling point [°C] : </td>
<td>
117°C</td>
</tr>
<tr>
<td>
Final boiling point [°C] : </td>
<td>
118°C</td>
</tr>
<tr>
<td>
Evaporation rate : </td>
<td>
0,97</td>
</tr>
<tr>
<td>
Vapour pressure [20°C] : </td>
<td>
15.2 hPa at 20°C</td>
</tr>
<tr>
<td>
Vapour pressure mm/Hg : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Vapour density : </td>
<td>
2,1</td>
</tr>
<tr>
<td>
Density [g/cm3] : </td>
<td>
1,049</td>
</tr>
<tr>
<td>
Relative density, gas (air=1) :</td>
<td>
N/A</td>
</tr>
<tr>
<td>
Relative density, liquid (water=1) :</td>
<td>
N/A</td>
</tr>
<tr>
<td>
Solubility in water [% weight] : </td>
<td>
Complete</td>
</tr>
<tr>
<td>
Solubility in water : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Log Pow octanol / water at 20°C :</td>
<td>
No data available.</td>
</tr>
<tr>
<td>
Solubility :</td>
<td>
2,4</td>
</tr>
<tr>
<td>
Viscosity at 40°C [mm2/s] : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Explosive properties : </td>
<td>
N/A</td>
</tr>
<tr>
<td>
Explosion limits - upper [%] : </td>
<td>
19,90%</td>
</tr>
<tr>
<td>
Explosion limits - lower [%] : </td>
<td>
4%</td>
</tr>
<tr>
<td>
Oxidising properties : </td>
<td>
No data available.</td>
</tr>
</tbody>
</table>
<p style="text-align: justify;">
<span style="font-size:12px;"><strong><span style="text-align: justify; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;"> It is convenient to use a sealed stirrer, such as the </span><span class="apparatus" style="text-align: justify; margin: 0px; padding: 0px; outline: none; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;">Trubore stirrer</span><span style="text-align: justify; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;">, which may be left in the flask during the distillation of </span><span class="chemname" style="text-align: justify; margin: 0px; padding: 0px; outline: none; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;"><span class="hotspot" style="margin: 0px; padding: 0px 0px 1px; outline: none; color: rgb(3, 74, 243); border-bottom: 1px dotted rgb(3, 74, 243); cursor: pointer;">thionyl chloride</span></span><span style="text-align: justify; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;"> and </span><span class="chemname" style="text-align: justify; margin: 0px; padding: 0px; outline: none; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;"><span class="hotspot" style="margin: 0px; padding: 0px 0px 1px; outline: none; color: rgb(3, 74, 243); border-bottom: 1px dotted rgb(3, 74, 243); cursor: pointer;">benzene</span></span><span style="text-align: justify; color: rgb(0, 0, 0); font-family: "Helvetica Neue", "Lucida Grande", "Segoe UI", Arial, Helvetica, Verdana, sans-serif;"> at reduced pressure; however, the stirrer cannot be left running during this distillation, for it is stopped by the cake of acid chloride hydrochloride. The distillations are accomplished most conveniently if the dropping funnel is removed and replaced by a capillary and the stirrer is left in place but not running during the distillations.</span></strong></span></p>
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