BenzalDehyde
BenzalDehyde supplier and exporter. Benzaldehyde (also called Benzenecarbonal) is the simplest representative of the aromatic aldehydes. It is a colorless liquid aldehyde with a characteristic almond odor. It boils at 180°C, is soluble in ethanol, but is insoluble in water.
Chemical intermediates for dyes, Flavouring Materials, Perfumes and Aromatic Alcohol Solvent for Oils, Resins, Some Cellulose ethers, Cellulose Acetate and Nitrate. Flavouring Compounds in Synthetic Perfumes. Manufacturing of Cinnamic Acid, Benzoic Acid, Pharmaceuticals, Photographic Chemicals.
Benzaldehyde is formed by partial oxidation of benzyl alcohol and readily oxidized to benzoic acid and is converted to addition products by hydrocyanic acid or sodium bisulfite. It is also prepared by oxidation of toluene or benzyl chloride or by treating benzal chloride with an alkali, e.g., sodium hydroxide.
It is used chiefly in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives and benzaldehyde is an important intermediate for the processing of perfume and flavouring compounds and in the preparation of certain aniline dyes . It is the first step in the synthesis for fragrances. It undergoes simultaneous oxidation and reduction with alcoholic potassium hydroxide, giving potassium benzoate and benzyl alcohol. It is converted to benzoin with alcoholic potassium cyanide, with anhydrous sodium acetate and acetic anhydride, giving cinnamic acid. Compounds which do not have alpha-hydrogen atoms cannot form an enolate ion and do not undergo electrophilic alpha-substitution and aldol condensation. Aromatic aldehydes such as benzaldehyde and formaldehyde may undergo disproportionation in concentrated alkali (Cannizaro's reaction); one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. The speed of the reaction depends on the substituents in the aromatic ring. Two different types of aldehydes (aromatic and aliphatic) can undergo crossing reaction to form fomaldehyde and aromatic alcohols.
| PRODUCT NAME | : | - BENZALDEHYDE |
| CAS number | : | - 100-52-7 |
| UN number | : | - 1990 |
| Formula | : | - C6H5CHO |
| Odour | : | - LIKE OIL OF BITTER ALMOND |
| Solubility in water | : | - SLIGHTLY |
| Density | : | - 1.041 at 25 oC |
| Boiling point | : | - 179 oC |
| Melting point | : | - -56 oC |
| Viscosity | : | - 1.39 cp at 25 oC |
| Flashpoint | : | - 62 oC |
| Explosive limits | : | - 1.4 - ? Vol% |
| Vapour pressure | : | - .93 mbar at 20 oC |
| Skin absorption/irritation | : | - YES |
| TLV Country | : | |
| Pollution category 1994 | : |
It is used chiefly in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives and benzaldehyde is an important intermediate for the processing of perfume and flavouring compounds and in the preparation of certain aniline dyes . It is the first step in the synthesis for fragrances. It undergoes simultaneous oxidation and reduction with alcoholic potassium hydroxide, giving potassium benzoate and benzyl alcohol. It is converted to benzoin with alcoholic potassium cyanide, with anhydrous sodium acetate and acetic anhydride, giving cinnamic acid. Compounds which do not have alpha-hydrogen atoms cannot form an enolate ion and do not undergo electrophilic alpha-substitution and aldol condensation. Aromatic aldehydes such as benzaldehyde and formaldehyde may undergo disproportionation in concentrated alkali (Cannizaro's reaction); one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. The speed of the reaction depends on the substituents in the aromatic ring. Two different types of aldehydes (aromatic and aliphatic) can undergo crossing reaction to form fomaldehyde and aromatic alcohols.
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