Key details
| Generic name | BENZOIN |
|---|---|
| Standard packing | 0.00 Box |
| Supply locations | [BENZOIN FOR SYNTHESIS] 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. [BENZOIN FOR SYNTHESIS] is available in small packing as well as in bulk. Buy premium quality [BBENZOIN FOR SYNTHESIS] and other lab chemicals from one of the most trusted brands. |
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<span style="font-size:14px;"><strong><span style="font-family: arial, sans-serif; color: rgb(32, 33, 36);">The reaction is helpful in </span><b style="font-family: arial, sans-serif; color: rgb(32, 33, 36); font-size: 16px;">the synthesis of heterocyclic compounds</b><span style="font-family: arial, sans-serif; color: rgb(32, 33, 36);"> and also extends to the aliphatic form of aldehydes.</span></strong></span></p>
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<span style="font-size:14px;"><strong style="font-size: 14px; text-align: justify;"><span style="color: rgb(95, 99, 104); font-family: arial, sans-serif;">Benzoin</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> Condensation is a coupling </span><span style="color: rgb(95, 99, 104); font-family: arial, sans-serif;">reaction</span><span style="color: rgb(77, 81, 86); font-family: arial, sans-serif;"> between two aldehydes that allows the preparation of α-hydroxyketones</span></strong></span></p>
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Physical state at 20 °C : </td>
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Solid</td>
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Odour threshold : </td>
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No data available </td>
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pH value :</td>
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No data available</td>
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Relative evaporation rate (butylacetate=1) :</td>
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No data available</td>
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Melting point : -</td>
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1 °C</td>
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Freezing point :</td>
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No data available</td>
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Boiling point : </td>
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344 °C Flash point : No data available</td>
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Auto-ignition temperature : </td>
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No data available</td>
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Decomposition temperature : </td>
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No data available</td>
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Flammability (solid, gas) :</td>
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No data available</td>
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Vapour pressure : </td>
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1.1 mm Hg at 135.60C</td>
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Relative vapour density at 20 °C :</td>
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No data available</td>
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Relative vapour density at 20 °C : </td>
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No data availableI </td>
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Relative density : </td>
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No data available</td>
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Solubility :</td>
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Water: Slightly soluble in water</td>
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Log Pow : </td>
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No data available</td>
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Viscosity, kinematic : </td>
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No data available</td>
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Viscosity, dynamic :</td>
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No data available</td>
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Explosive properties : </td>
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No data available</td>
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Oxidising properties :</td>
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No data available</td>
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Explosive limits :</td>
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No data available</td>
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<strong><span style="color: rgb(32, 33, 34); font-family: sans-serif;">The main uses of benzoin are as a precursor to </span><a href="https://en.wikipedia.org/wiki/Benzil" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Benzil">benzil</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">, which is a </span><a href="https://en.wikipedia.org/wiki/Photoinitiator" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Photoinitiator">photoinitiator</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> The conversion proceeds by </span><a class="mw-redirect" href="https://en.wikipedia.org/wiki/Organic_oxidation" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Organic oxidation">organic oxidation</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> using copper(II),</span><span style="color: rgb(32, 33, 34); font-family: sans-serif;"> </span><a href="https://en.wikipedia.org/wiki/Nitric_acid" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Nitric acid">nitric acid</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">, or </span><a class="mw-redirect" href="https://en.wikipedia.org/wiki/Oxone" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Oxone">oxone</a>.</strong></p>
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<strong><span style="color: rgb(32, 33, 34); font-family: sans-serif;">Benzoin can be used in the preparation of several pharmaceutical drugs including </span><a href="https://en.wikipedia.org/wiki/Oxaprozin" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Oxaprozin">oxaprozin</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">, </span><a href="https://en.wikipedia.org/wiki/Ditazole" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Ditazole">ditazole</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">, and </span><a href="https://en.wikipedia.org/wiki/Phenytoin" style="text-decoration-line: none; color: rgb(6, 69, 173); background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: sans-serif; font-size: 14px;" title="Phenytoin">phenytoin</a><span style="color: rgb(32, 33, 34); font-family: sans-serif;">.</span></strong></p>
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