Key details
| Standard packing | 0.00 Box |
|---|---|
| Supply locations | BENZOPHENONE OXIME manufacturers, suppliers, exporters in Mumbai, Gandhidham, Kolkata, Varanasi, Visakhapatnam, Chennai, Fujairah, Dubai, Canada BC, Barka, Sohar, Muscat, Oman. Lab chemicals manufacturers, suppliers, exporters in India, UAE Middle East, Barka, Sohar, Muscat, Oman, Canada. BENZOPHENONE OXIME is available in small packing as well as in bulk. Buy premium quality BENZOPHENONE OXIME and other lab chemicals from one of the most trusted brands. |
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<span style="font-size:14px;"><strong><span style="color: rgb(32, 33, 36); font-family: arial, sans-serif;"> </span>BENZOPHENONE OXIME <span style="color: rgb(32, 33, 36); font-family: arial, sans-serif;">a reagent for the </span><b style="color: rgb(32, 33, 36); font-family: arial, sans-serif; font-size: 16px;">colorimetric determination of urea</b><span style="color: rgb(32, 33, 36); font-family: arial, sans-serif;"> and ureido compounds. Oxime is used as a ligand in transition-metal complex catalyst chemistry. Oxime acts as an antioxidant, radical scavenger which find applications in textile, plastic, paint, detergent, and rubber industry. </span></strong></span></p>
<p style="text-align: justify;">
<strong><span style="font-weight: bold; color: rgb(95, 99, 104); font-family: arial, sans-serif;">Benzophenone</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> is used as an ultraviolet (UV)-curing agent in sunglasses, ... and was approximately 70% of the </span><span style="font-weight: bold; color: rgb(95, 99, 104); font-family: arial, sans-serif;">dose</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> applied to occluded skin within 24 hours.</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>
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:14px;"><strong><span style="color: rgb(32, 33, 34); font-family: sans-serif;">Oximes are usually generated by the reaction of </span><a href="https://en.wikipedia.org/wiki/Hydroxylamine" style="background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; text-decoration-line: none; color: rgb(6, 69, 173); font-family: sans-serif; font-size: 14px;" title="Hydroxylamine">hydroxylamine</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> with </span><a href="https://en.wikipedia.org/wiki/Aldehyde" style="background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; text-decoration-line: none; color: rgb(6, 69, 173); font-family: sans-serif; font-size: 14px;" title="Aldehyde">aldehydes</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> or </span><a href="https://en.wikipedia.org/wiki/Ketone" style="background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; text-decoration-line: none; color: rgb(6, 69, 173); font-family: sans-serif; font-size: 14px;" title="Ketone">ketones</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">. The term oxime dates back to the 19th century, a combination of the words </span><i style="color: rgb(32, 33, 34); font-family: sans-serif; font-size: 14px;">oxygen</i><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> and </span><i style="color: rgb(32, 33, 34); font-family: sans-serif; font-size: 14px;">imine.</i></strong></span></p>
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