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Benzaldehyde
[CAS# 100-52-7]

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Complete supplier list of Benzaldehyde
Identification
Classification Organic raw materials >> Aldehyde
Name Benzaldehyde
Synonyms Benzoic aldehyde; Phenylmethanal
Molecular Structure CAS # 100-52-7, Benzaldehyde, Benzoic aldehyde, Phenylmethanal
Molecular Formula C7H6O
Molecular Weight 106.12
CAS Registry Number 100-52-7
EC Number 202-860-4
FEMA 2127
SMILES C1=CC=C(C=C1)C=O
Properties
Density 1.044 g/mL (20 ºC) (Expl.)
Melting point -26 ºC (Expl.)
Boiling point 179 ºC (Expl.)
Refractive index 1.545 (Expl.)
Flash point 64 ºC (Expl.)
Water solubility <0.01 g/100 mL (19.5 ºC) (Expl.)
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H319-H332-H336    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P304+P340-P305+P351+P338-P317-P319-P330-P337+P317-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H332
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H336
Specific target organ toxicity - single exposureSTOT SE3H335
Skin sensitizationSkin Sens.1H317
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Reproductive toxicityRepr.1BH360D
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Acute toxicityAcute Tox.3H331
Acute toxicityAcute Tox.4H312
Specific target organ toxicity - repeated exposureSTOT RE2H373
Reproductive toxicityRepr.1BH360
Transport Information UN 1989
SDS Available
up Discovory and Applicatios
Benzaldehyde is a simple aromatic aldehyde with the molecular formula C₆H₅CHO. It is one of the most important and widely used aromatic compounds in both organic synthesis and industrial applications. Benzaldehyde was first isolated in the early 19th century from bitter almonds, a natural source of the compound, and its distinctive almond-like odor has made it an important ingredient in flavoring and fragrance industries. Its discovery and the development of its applications have contributed to a variety of fields, including pharmaceuticals, cosmetics, and materials science.

The first recorded synthesis of benzaldehyde is attributed to the German chemist, August Wilhelm von Hofmann, in 1855. Hofmann synthesized the compound by oxidizing toluene, a methylated benzene derivative, using chromic acid. This marked a significant advancement in the ability to produce benzaldehyde synthetically, as prior to this, it was primarily obtained through the distillation of bitter almonds, where it occurs as part of the cyanogenic glycoside amygdalin. Over time, other methods of synthesizing benzaldehyde were developed, such as the oxidation of toluene or the reaction of benzyl chloride with sodium hydroxide.

Benzaldehyde is characterized by its aromatic odor, which is often associated with almonds, cherries, or certain flowers, making it highly useful in the production of flavors and fragrances. It is a key ingredient in almond-flavored products and is also used in the fragrance industry to impart a sweet, nutty scent. Beyond its use in flavorings and perfumes, benzaldehyde plays a significant role as a building block in the synthesis of various chemicals. It is a precursor in the production of other compounds like cinnamic acid, benzoin, and certain pharmaceuticals. Additionally, benzaldehyde serves as a starting material in the preparation of plastics, dyes, and resins.

In the pharmaceutical industry, benzaldehyde is used as an intermediate in the synthesis of a range of active pharmaceutical ingredients (APIs), including those used in the treatment of cardiovascular diseases, antimicrobial agents, and anti-inflammatory drugs. Its utility in medicinal chemistry arises from its ability to undergo various chemical reactions, such as condensation, reduction, and substitution, which allow the production of a wide array of biologically active compounds.

Another important application of benzaldehyde is in the synthesis of benzoin, a compound with antiseptic properties, which is further used to prepare benzoin derivatives. It also serves as a key reactant in the production of plastics, where its reactivity enables the formation of polymers and resins. Furthermore, benzaldehyde is employed in the synthesis of various specialty chemicals, including rubber accelerators and dyes.

Benzaldehyde has a relatively low toxicity, but exposure to high concentrations can cause irritation to the eyes, skin, and respiratory system. As with many chemicals, proper handling and safety protocols are necessary to minimize risks during its production and use.

In conclusion, benzaldehyde is a versatile and widely used compound in industries ranging from food and cosmetics to pharmaceuticals and material science. Its distinct odor, chemical reactivity, and role as a precursor to a variety of other chemicals make it a valuable substance in both industrial and laboratory settings. As research continues into its applications, new uses for benzaldehyde may emerge, further cementing its importance in modern chemistry.
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