trans-Cinnamaldehyde
- CAS No.
- 14371-10-9
- Chemical Name:
- trans-Cinnamaldehyde
- Synonyms
- (E)-Cinnamaldehyde;3-Phenyl-2-propenal;STYRONE;(2E)-3-Phenylprop-2-enal;FEMA 2286;3-PHENYLPROPENAL;(E)-3-Phenylpropenal;trans-Cinnamylaldehyde;(e)-3-phenyl-2-propenal;Cinna-mal
- CBNumber:
- CB9168460
- Molecular Formula:
- C9H8O
- Molecular Weight:
- 132.16
- MOL File:
- 14371-10-9.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/4/26 17:21:34
| Melting point | −9-−4 °C(lit.) |
|---|---|
| Boiling point | 250-252 °C(lit.) |
| Density | 1.05 g/mL at 25 °C(lit.) |
| vapor density | 4.6 (vs air) |
| refractive index |
n |
| FEMA | 2286 | CINNAMALDEHYDE |
| Flash point | 160 °F |
| storage temp. | 2-8°C |
| solubility | Chloroform (Slightly), DMSO (Sparingly), Methanol (Slightly) |
| form | Liquid |
| color | Clear yellow |
| Odor | at 10.00 % in dipropylene glycol. sweet spice candy cinnamon red hots warm |
| Odor Type | spicy |
| Water Solubility | 1.1 g/L (20 ºC) |
| Sensitive | Air Sensitive |
| Merck | 14,2297 |
| JECFA Number | 656 |
| BRN | 1071571 |
| Dielectric constant | 16.899999999999999 |
| Stability | Hygroscopic |
| LogP | 1.820 |
| CAS DataBase Reference | 14371-10-9(CAS DataBase Reference) |
| NIST Chemistry Reference | Cinnamaldehyde, (E)-(14371-10-9) |
| EPA Substance Registry System | trans-Cinnamaldehyde (14371-10-9) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H315-H317-H319-H335 | |||||||||
| Precautionary statements | P261-P264-P271-P280-P302+P352-P305+P351+P338 | |||||||||
| Hazard Codes | Xi,Xn | |||||||||
| Risk Statements | 36/37/38-43-21 | |||||||||
| Safety Statements | 26-36/37-37/39-24 | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | GD6476000 | |||||||||
| F | 10-23 | |||||||||
| HS Code | 29122990 | |||||||||
| NFPA 704 |
|
trans-Cinnamaldehyde price More Price(16)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | W228605 | trans-Cinnamaldehyde FCC, FG | 14371-10-9 | 1SAMPLE-K | ₹5141.88 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W228605 | trans-Cinnamaldehyde FCC, FG | 14371-10-9 | 1KG | ₹6852.23 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W228605 | trans-Cinnamaldehyde FCC, FG | 14371-10-9 | 10KG | ₹22418.58 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | W228605 | trans-Cinnamaldehyde FCC, FG | 14371-10-9 | 25KG | ₹41697.9 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | C80687 | trans-Cinnamaldehyde 99% | 14371-10-9 | 25G | ₹2284.08 | 2022-06-14 | Buy |
trans-Cinnamaldehyde Chemical Properties,Uses,Production
Chemical Properties
trans-Cinnamaldehyde is the
main component of cassia oil (about 90%) and Sri Lanka cinnamon bark oil (about 75%). Smaller quantities are found in many other essential oils. In nature, the
trans-isomer is predominant.
trans-Cinnamaldehyde is a yellowish liquid with a characteristic spicy odor,
strongly reminiscent of cinnamon. Being an ??,??-unsaturated aldehyde, it
undergoes many reactions, of which hydrogenation to cinnamic alcohol, dihydrocinnamaldehyde,
and dihydrocinnamic alcohol is important. Cinnamic acid is
formed by autoxidation.
On an industrial scale, cinnamaldehyde is prepared almost exclusively by
alkaline condensation of benzaldehyde and acetaldehyde. Self-condensation of
acetaldehyde can be avoided by using an excess of benzaldehyde and by slowly
adding acetaldehyde.
Cinnamaldehyde is used in many compositions for creating spicy and oriental
notes (e.g., soap perfumes). It is the main component of artificial cinnamon oil. In
addition, it is an important intermediate in the synthesis of cinnamic alcohol and
dihydrocinnamic alcohol.
Uses
trans-Cinnamaldehyde is used in the flavor and perfume industry. It is also used in medicine. It reacts with glutathione to get an adduct 1'-(glutathion-S-yl)-dihydrocinnamaldehyde. It is used to prepare cinnamylidene-bisacetamide by reacting with acetamide. Further, it inhibits xanthine oxidase.
Definition
ChEBI: The E (trans) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes.
General Description
Clear yellow liquid with an odor of cinnamon and a sweet taste.
Air & Water Reactions
May be sensitive to prolonged exposure to air and light. Insoluble in water.
Reactivity Profile
trans-Cinnamaldehyde is incompatible with strong oxidizing agents and strong bases. trans-Cinnamaldehyde can also react with sodium hydroxide.
Fire Hazard
trans-Cinnamaldehyde is combustible.
Potential Exposure
Botanical fungicide and insecticide. Used as an antifungal agent, corn rootworm attractant, and dog and cat repellent. Can be used on soil casing for mushrooms, row crops, turf, and all food commodities. Not listed for use in EU countries.
Shipping
UN1989 Aldehydes, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid
Incompatibilities
Aldehydes are frequently involved in selfcondensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, ketones, azo dyes, caustics, boranes, hydrazines
Waste Disposal
Incineration. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.
trans-Cinnamaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
1of3
chevron_right| Supplier | Tel | Country | ProdList | Advantage | Inquiry |
|---|---|---|---|---|---|
| JSK Chemicals | +919879767970 | Gujarat, India | 3756 | 58 | Inquiry |
| Avra Synthesis Pvt Ltd | +914027175796 | New Delhi, India | 1606 | 30 | Inquiry |
| Clearsynth Labs | 91-22-45045900 | Maharashtra, India | 3889 | 58 | Inquiry |
| Oceanic Pharmachem Pvt. Ltd. | 91-22-42128600 | Maharashtra, India | 2006 | 58 | Inquiry |
| ASM Organics | 91-9866122393 | Andhra Pradesh, India | 1188 | 58 | Inquiry |
| Pharma Affiliates | 172-5066494 | Haryana, India | 6761 | 58 | Inquiry |
| Anand Agencies | 91-20-24454597 | Maharashtra, India | 2337 | 58 | Inquiry |
| Spectrochem Private Limited | 08048372608Ext 246 | Maharashtra, India | 1056 | 58 | Inquiry |
| Dr Prem's Molecules Pvt. Ltd. | +91 9825310038 | New Delhi, India | 547 | 50 | Inquiry |
| CLEARSYNTH LABS LTD. | +91-22-45045900 | Hyderabad, India | 6351 | 58 | Inquiry |
| Supplier | Advantage |
|---|---|
| JSK Chemicals | 58 |
| Avra Synthesis Pvt Ltd | 30 |
| Clearsynth Labs | 58 |
| Oceanic Pharmachem Pvt. Ltd. | 58 |
| ASM Organics | 58 |
| Pharma Affiliates | 58 |
| Anand Agencies | 58 |
| Spectrochem Private Limited | 58 |
| Dr Prem's Molecules Pvt. Ltd. | 50 |
| CLEARSYNTH LABS LTD. | 58 |
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