Key details
| Generic name | BENZALDEHYDE |
|---|---|
| Standard packing | 0.00 Box |
| Supply locations | BENZALDEHYDE LR 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. BENZALDEHYDE LR is available in small packing as well as in bulk. Buy premium quality BENZALDEHYDE LR and other lab chemicals from one of the most trusted brands. |
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<span class="ILfuVd NA6bn UiGGAb"><span class="hgKElc"><b>Benzaldehyde</b> (C<sub>6</sub>H<sub>5</sub>CHO), the simplest representative of the aromatic aldehydes, occurring naturally as the glycoside amygdalin. Prepared synthetically, it is <b>used</b> chiefly in the manufacture of dyes, cinnamic acid, and other organic compounds, and to some extent in perfumes and flavouring agents.</span></span></p>
<p>
Benzaldehyde undergoes disproportionation upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid Benzaldehyde undergoes disproportionation upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </p>
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<a href="http://tiwariindia.com/work/index.php?module=Products&action=DetailView…; style="text-decoration-line: none; color: rgb(0, 112, 186);" title="Products">BENEDICT’S REAGENT QUANTITATIVE</a></td>
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<div aria-level="3" class="LGOjhe" data-attrid="wa:/description" data-hveid="CCkQAA" role="heading" style="overflow: hidden; padding-bottom: 20px;">
<span class="ILfuVd NA6bn c3biWd" style="font-size: 16px; line-height: 24px;"><span class="hgKElc" style="padding: 0px 8px 0px 0px;">Benzaldehyde undergoes <b>disproportionation</b> upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </span></span></div>
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<a href="http://tiwariindia.com/work/index.php?module=Products&action=DetailView…; style="text-decoration-line: none; color: rgb(0, 112, 186);" title="Products">BENEDICT’S REAGENT QUANTITATIVE</a></td>
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<a href="http://tiwariindia.com/work/index.php?module=Products&action=DetailView…; style="text-decoration-line: none; color: rgb(0, 112, 186);" title="Products">BENEDICT’S REAGENT QUANTITATIVE</a></td>
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<div class="t0bRye a2qtDc r2fjmd" data-hveid="CDQQBA" data-ved="2ahUKEwjH-vO__rzzAhWwzjgGHaqcBnEQu04oAHoECDQQBA" id="_LF1hYce0MbCd4-EPqrmaiAc86" jsname="oQYOj" style="margin-bottom: 0px; margin-top: 0px; opacity: 1;">
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<div aria-level="3" class="LGOjhe" data-attrid="wa:/description" data-hveid="CCkQAA" role="heading" style="overflow: hidden; padding-bottom: 20px;">
<span class="ILfuVd NA6bn c3biWd" style="font-size: 16px; line-height: 24px;"><span class="hgKElc" style="padding: 0px 8px 0px 0px;">Benzaldehyde undergoes <b>disproportionation</b> upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </span></span></div>
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<a href="http://tiwariindia.com/work/index.php?module=Products&action=DetailView…; style="text-decoration-line: none; color: rgb(0, 112, 186);" title="Products">BENEDICT’S REAGENT QUANTITATIVE</a></td>
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<div aria-level="3" class="LGOjhe" data-attrid="wa:/description" data-hveid="CCkQAA" role="heading" style="overflow: hidden; padding-bottom: 20px;">
<span class="ILfuVd NA6bn c3biWd" style="font-size: 16px; line-height: 24px;"><span class="hgKElc" style="padding: 0px 8px 0px 0px;">Benzaldehyde undergoes <b>disproportionation</b> upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </span></span></div>
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<a href="http://tiwariindia.com/work/index.php?module=Products&action=DetailView…; style="text-decoration-line: none; color: rgb(0, 112, 186);" title="Products">BENEDICT’S REAGENT QUANTITATIVE</a></td>
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<div aria-level="3" class="LGOjhe" data-attrid="wa:/description" data-hveid="CCkQAA" role="heading" style="overflow: hidden; padding-bottom: 20px;">
<span class="ILfuVd NA6bn c3biWd" style="font-size: 16px; line-height: 24px;"><span class="hgKElc" style="padding: 0px 8px 0px 0px;">Benzaldehyde undergoes <b>disproportionation</b> upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </span></span></div>
</div>
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</div>
</div>
</div>
</div>
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<span class="ILfuVd NA6bn c3biWd" style="font-size: 16px; line-height: 24px;"><span class="hgKElc" style="padding: 0px 8px 0px 0px;">Benzaldehyde undergoes <b>disproportionation</b> upon treatment with concentrated alkali one molecule of the aldehyde is reduced to the benzyl alcohol and another molecule is simultaneously oxidized to benzoic acid. </span></span></div>
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Physical state at 20 °C : Liquid.</div>
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Odour : characteristic odor</div>
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Odour threshold : No data available.</div>
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pH value : Not applicable.</div>
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Melting point [°C] : - 26 °C</div>
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Decomposition point [°C] : N/A</div>
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Critical temperature [°C] : N/A</div>
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Auto-ignition temperature [°C] : N/A</div>
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Flammability (solid, gas) : N/A</div>
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Flash point [°C] : 64 °C</div>
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Boiling point [°C] : 177 - 179 °C</div>
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Initial boiling point [°C] : 177 °C</div>
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Final boiling point [°C] : 179 °C</div>
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Evaporation rate : N/A</div>
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Vapour pressure [20°C] : N/A</div>
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Vapour pressure mm/Hg : 1 mm Hg @ 260C</div>
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Vapour density : 3,66</div>
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Density [g/cm3] : 1,05</div>
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Relative density, gas (air=1) : N/A</div>
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Relative density, liquid (water=1) : N/A</div>
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Solubility in water [% weight] : Slightly soluble in</div>
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Solubility in water : N/A</div>
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Log Pow octanol / water at 20°C : No data available.</div>
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Solubility : 5,9</div>
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Viscosity at 40°C [mm2/s] : N/A</div>
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Explosive properties : N/A</div>
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Explosion limits - upper [%] : 8,50%</div>
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Explosion limits - lower [%] : 1,40%</div>
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Oxidising properties : No data available</div>
<p style="text-align: justify;">
The azlactone of α-acetaminocinnamic acid may also be prepared by substituting the equivalent amount of glycine for acetylglycine and increasing the amount of acetic anhydride to three molecular proportions, but the yield is only about 45–50 per cent of the theoretical amount.</p>
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