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trans-Cinnamaldehyde
[CAS# 14371-10-9]

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Complete supplier list of trans-Cinnamaldehyde
Identification
Classification Flavors and spices >> Synthetic spice >> Aldehyde fragrance >> Aromatic aldehyde
Name trans-Cinnamaldehyde
Synonyms 3-Phenyl-2-propenal
Molecular Structure CAS # 14371-10-9, trans-Cinnamaldehyde, 3-Phenyl-2-propenal
Molecular Formula C9H8O
Molecular Weight 132.16
CAS Registry Number 14371-10-9
EC Number 604-377-8
SMILES C1=CC=C(C=C1)/C=C/C=O
Properties
Water solubility 1.1 g/L (20 ºC)
Density 1.0±0.1 g/mL, Calc.*,1.05 g/mL (Expl.)
Melting point -9--4 ºC (Expl.)
Index of Refraction 1.577, Calc.*, 1.622 (Expl.)
Boiling Point 246.8±9.0 ºC (760 mmHg), Calc.*, 250-252 ºC (Expl.)
Flash Point 71.1 ºC, Calc.*, 71 ºC (Expl.)
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H312-H315-H317-H319-H335-H412    Details
Precautionary Statements P261-P264-P264+P265-P271-P272-P273-P280-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P332+P317-P333+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Skin sensitizationSkin Sens.1H317
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Flammable liquidsFlam. Liq.4H227
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
Trans-cinnamaldehyde, with the chemical formula C9H8O, is a naturally occurring organic compound found in the essential oil of cinnamon bark. It is the major component of cinnamon oil and contributes significantly to the characteristic odor and flavor of cinnamon. The compound consists of a cinnamyl group attached to an aldehyde functional group, giving it its distinctive aromatic properties.

Trans-cinnamaldehyde was first isolated from cinnamon oil in the early 19th century, and its structure was determined through chemical analysis. It is a yellowish liquid with a strong, sweet, spicy odor, widely recognized as a key element in cinnamon's fragrance profile.

Trans-cinnamaldehyde is primarily used in the flavor and fragrance industries due to its pleasant, spicy aroma. It is used in the formulation of perfumes, soaps, and cosmetics. In the food industry, trans-cinnamaldehyde is used as a flavoring agent, imparting a cinnamon-like taste to various products, including baked goods, candies, and beverages.

In addition to its applications in flavor and fragrance, trans-cinnamaldehyde has demonstrated various biological activities, which have been studied in the context of food preservation, medicinal applications, and potential therapeutic uses. It has been shown to possess antimicrobial, antifungal, and antioxidant properties, making it valuable for use in preservatives, sanitizers, and as a potential component in therapeutic formulations.

The compound has also been studied for its potential pharmacological properties. Research indicates that trans-cinnamaldehyde may have anti-inflammatory, analgesic, and anticancer effects, though these applications are still under investigation. It is also being explored for its potential to enhance the bioavailability of certain drugs or to act as a delivery agent for pharmaceutical compounds.

Trans-cinnamaldehyde is considered to be of low toxicity in the concentrations typically used in food and cosmetic products. However, in high concentrations, it can cause irritation to the skin and mucous membranes. Standard safety precautions should be followed when handling the compound, particularly in concentrated forms.

In summary, trans-cinnamaldehyde is a widely used and versatile compound, valued for its distinctive aromatic properties and its applications in the flavor, fragrance, and chemical industries. Its potential biological and pharmacological activities continue to be explored, broadening its scope of applications in both consumer products and medical research.

References

2024. Enhanced synergistic antioxidant and antibacterial effects of stable nanoemulsions prepared from blends of thyme, black pepper, cinnamon, and garlic essential oils. BioNanoScience, 14(4).
DOI: 10.1007/s12668-024-01718-0

2012. Kinetics of thermal destruction of Salmonella in ground chicken containing trans-Cinnamaldehyde and carvacrol. Journal of Food Protection, 75(2).
DOI: 10.4315/0362-028x.jfp-11-307

2010. The cinnamon-derived dietary factor cinnamic aldehyde activates the Nrf2-dependent antioxidant response in human epithelial colon cells. Molecules (Basel, Switzerland), 15(5).
DOI: 10.3390/molecules15053338
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