Benzaldehyde |
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Benzaldehyde 100-52-7 Chemical Properties Colorless to light yellow liquid |
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100-52-7 |
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Product Name: Benzaldehyde Synonyms: Almond artificial essential oil almondartificialessentialoil Artifical essential oil of almond Artificial Almond Oil Artificial bitter almond oil artificialalmondoil Benzaldehyde FFC benzaldehydeffc CAS: 100-52-7 MF: C7H6O MW: 106.12 EINECS: 202-860-4 mp -26 ¡ÆC bp 179 ¡ÆC density 1.05 vapor density 3.7 (vs air) vapor pressure 4 mm Hg ( 45 ¡ÆC) FEMA 2127 refractive index n20/D 1.545(lit.) Fp 145 ¡ÆF Water Solubility <0.01 g/100 mL at 19.5 ¨¬C Chemical Properties Colorless to light yellow liquid Reactivity Profile A nontoxic, combustible liquid, reacts with oxidizing reagents. Benzaldehyde must be blanketed with an inert gas at all times since Benzaldehyde is oxidized readily by air to benzoic acid [Kirk-Othmer, 3rd ed., Vol. 3, 1978, p. 736]. In contact with strong acids or bases Benzaldehyde will undergo an exothermic condensation reaction [Sax, 9th ed., 1996, p. 327]. A violent reaction was observed on contact with peroxyacids (peroxyformic acid) [DiAns, J. et al., Ber., 1915, 48, p. 1136]. An explosion occurred when pyrrolidine, Benzaldehyde, and propionic acid were heated to form porphyrins.
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Product Name: Benzaldehyde Synonyms: Almond artificial essential oil almondartificialessentialoil Artifical essential oil of almond Artificial Almond Oil Artificial bitter almond oil artificialalmondoil Benzaldehyde FFC benzaldehydeffc CAS: 100-52-7 MF: C7H6O MW: 106.12 EINECS: 202-860-4 mp -26 ¡ÆC bp 179 ¡ÆC density 1.05 vapor density 3.7 (vs air) vapor pressure 4 mm Hg ( 45 ¡ÆC) FEMA 2127 refractive index n20/D 1.545(lit.) Fp 145 ¡ÆF Water Solubility <0.01 g/100 mL at 19.5 ¨¬C Chemical Properties Colorless to light yellow liquid Reactivity Profile A nontoxic, combustible liquid, reacts with oxidizing reagents. Benzaldehyde must be blanketed with an inert gas at all times since Benzaldehyde is oxidized readily by air to benzoic acid [Kirk-Othmer, 3rd ed., Vol. 3, 1978, p. 736]. In contact with strong acids or bases Benzaldehyde will undergo an exothermic condensation reaction [Sax, 9th ed., 1996, p. 327]. A violent reaction was observed on contact with peroxyacids (peroxyformic acid) [DiAns, J. et al., Ber., 1915, 48, p. 1136]. An explosion occurred when pyrrolidine, Benzaldehyde, and propionic acid were heated to form porphyrins.
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