| Product Name: Benzaldehyde |
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| FFC;benzaldehydeffc |
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| CAS: 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 °C
bp 179 °C
density 1.05
vapor density 3.7 (vs air)
vapor pressure 4 mm Hg ( 45 °C)
FEMA 2127
refractive index n20/D 1.545(lit.)
Fp 145 °F
Water Solubility <0.01 g/100 mL at 19.5 ºC
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.
Benzoic aldehyde derivates: Benzaldehyde, Anisic aldehyde, Veratraldehyde, TMBA, Salicylaldehyde, PHBA, m-Hydroxybenzaldehyde, Protocatechualdehyde, o-Nitrobenzaldehyde, m-Nitrobenzaldehyde, p, Nitrobenzaldehyde, 2-Fluorobenzaldehyde, PFAD, p-Trifluoromethylbenzaldehyde, p-Benzyloxybenzaldehyde, o-Bromobenzaldehyde, 2-Cyanobenzaldehyde, Sodium 2-formylbenzenesulfonate, etc.
Benzoic acid derivates: Benzoate, DABA, Dinitrobenzoic acid, 4-Amino-3-nitrobenzoic acid, 4-Amino-3-methylbenzoic acid, 3-Methoxysalicylic acid, 3-hydroxyanthranilic acid hydrochloride, 2-Amino-5-iodobenzoic acid, 2-Amino-5-nitrobenzoic acid, 2-Amino-5-bromobenzoic acid, 2-Amino-6-chlorobenzoic acid, 2-Chloro-5-nitrobenzoic acid, 4-Chloro-3-sulfomulbenzoic acid, m-Aminobenzoic acid, p-Aminobenzoic acid, o-Nitrobenzoic acid, o-Bromobenzoic acid, o-Iodobenzoic acid, p-Ethoxybenzoic acid, etc.
Benzoate derivates: Benzyl benzoate, Ethylparaben, Sodium Ethylparaben, Propylparaben, Butylparaben, Sodium Butylparaben, Sodium methylparaben, Sodium propylparaben, Butyl p-aminobenzoate, Ethyl p-butylaminobenzoate, Ethyl p-dimethylaminobenzoate, Padimate, Octyl p-dimethylaminobenzoate, Methyl p-bromobenzoate, Methyl 4-(bromomethyl)benzoate, Methyl 2-bromobenzoate, Benzoic anhydride, etc.
Benzoic alcohol derivates: Benzyl alcohol, 3 4 5-Trimethoxybenzyl alcohol, 3 5-Dinitrobenzyl alcohol, 4-Mercaptobenzyl alcohol, Benzhydrol, etc.
Ms. Julia ycgc_int04@yccreate.com
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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 °C
bp 179 °C
density 1.05
vapor density 3.7 (vs air)
vapor pressure 4 mm Hg ( 45 °C)
FEMA 2127
refractive index n20/D 1.545(lit.)
Fp 145 °F
Water Solubility <0.01 g/100 mL at 19.5 ºC
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.
Benzoic aldehyde derivates: Benzaldehyde, Anisic aldehyde, Veratraldehyde, TMBA, Salicylaldehyde, PHBA, m-Hydroxybenzaldehyde, Protocatechualdehyde, o-Nitrobenzaldehyde, m-Nitrobenzaldehyde, p, Nitrobenzaldehyde, 2-Fluorobenzaldehyde, PFAD, p-Trifluoromethylbenzaldehyde, p-Benzyloxybenzaldehyde, o-Bromobenzaldehyde, 2-Cyanobenzaldehyde, Sodium 2-formylbenzenesulfonate, etc.
Benzoic acid derivates: Benzoate, DABA, Dinitrobenzoic acid, 4-Amino-3-nitrobenzoic acid, 4-Amino-3-methylbenzoic acid, 3-Methoxysalicylic acid, 3-hydroxyanthranilic acid hydrochloride, 2-Amino-5-iodobenzoic acid, 2-Amino-5-nitrobenzoic acid, 2-Amino-5-bromobenzoic acid, 2-Amino-6-chlorobenzoic acid, 2-Chloro-5-nitrobenzoic acid, 4-Chloro-3-sulfomulbenzoic acid, m-Aminobenzoic acid, p-Aminobenzoic acid, o-Nitrobenzoic acid, o-Bromobenzoic acid, o-Iodobenzoic acid, p-Ethoxybenzoic acid, etc.
Benzoate derivates: Benzyl benzoate, Ethylparaben, Sodium Ethylparaben, Propylparaben, Butylparaben, Sodium Butylparaben, Sodium methylparaben, Sodium propylparaben, Butyl p-aminobenzoate, Ethyl p-butylaminobenzoate, Ethyl p-dimethylaminobenzoate, Padimate, Octyl p-dimethylaminobenzoate, Methyl p-bromobenzoate, Methyl 4-(bromomethyl)benzoate, Methyl 2-bromobenzoate, Benzoic anhydride, etc.
Benzoic alcohol derivates: Benzyl alcohol, 3 4 5-Trimethoxybenzyl alcohol, 3 5-Dinitrobenzyl alcohol, 4-Mercaptobenzyl alcohol, Benzhydrol, etc.
Ms. Julia ycgc_int04@yccreate.com
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