ChemicalBook >> CAS DataBase List >>Cinnamaldehyde

Cinnamaldehyde

CAS No.
104-55-2
Chemical Name:
Cinnamaldehyde
Synonyms
CINNAMIC ALDEHYDE;3-Phenyl-2-propenal;2-Propenal, 3-phenyl-;STYRONE;3-Phenylacrylaldehyde;203-213-9;FEMA 2286;3-PHENYLPROPENAL;2-propenal,3-phenyl-;abionca
CBNumber:
CB1168459
Molecular Formula:
C9H8O
Lewis structure
c9h8o lewis structure
Molecular Weight:
132.16
MDL Number:
MFCD00007000
MOL File:
104-55-2.mol
MSDS File:
SDS
Last updated:2024-03-11 13:16:07

Cinnamaldehyde Properties

Melting point −9-−4 °C(lit.)
Boiling point 248 °C (lit.)
Density 1.05 g/mL at 25 °C (lit.)
vapor density 4.6 (vs air)
vapor pressure <0.1 hPa (20 °C)
FEMA 2286 | CINNAMALDEHYDE
refractive index n20/D 1.622(lit.)
Flash point 160 °F
storage temp. Store below +30°C.
solubility 1g/l soluble
form Liquid
pka 0[at 20 ℃]
color Clear yellow
Specific Gravity 1.05
Odor Strong odor of cinnamon
Odor Type spicy
Viscosity 21.25mm2/s
Water Solubility Slightly soluble
Merck 13,2319
JECFA Number 656
Dielectric constant 16.9(24℃)
Stability Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
InChIKey KJPRLNWUNMBNBZ-QPJJXVBHSA-N
LogP 1.83-2.1 at 25-27℃
Substances Added to Food (formerly EAFUS) CINNAMALDEHYDE
FDA 21 CFR 182.60
CAS DataBase Reference 104-55-2(CAS DataBase Reference)
FDA UNII SR60A3XG0F
NIST Chemistry Reference Cinnamylaldehyde(104-55-2)
EPA Substance Registry System Cinnamaldehyde (104-55-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H317-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38-43
Safety Statements  26-36/37
RIDADR  UN8027
WGK Germany  3
RTECS  GD6476000
10-23
HS Code  29122900
Toxicity LD50 in rats (mg/kg): 2220 orally (Jenner)

Cinnamaldehyde price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W228613 Cinnamaldehyde natural, ≥95%, FG 104-55-2 sample-k $38.2 2024-03-01 Buy
Sigma-Aldrich W228613 Cinnamaldehyde natural, ≥95%, FG 104-55-2 100g $81.9 2024-03-01 Buy
Sigma-Aldrich W228613 Cinnamaldehyde natural, ≥95%, FG 104-55-2 1kg $195 2024-03-01 Buy
Sigma-Aldrich W228613 Cinnamaldehyde natural, ≥95%, FG 104-55-2 5kg $777 2024-03-01 Buy
Sigma-Aldrich 8.02505 trans-Cinnamaldehyde forsynthesis 104-55-2 5ml $53.4 2024-03-01 Buy
Product number Packaging Price Buy
W228613 sample-k $38.2 Buy
W228613 100g $81.9 Buy
W228613 1kg $195 Buy
W228613 5kg $777 Buy
8.02505 5ml $53.4 Buy

Cinnamaldehyde Chemical Properties,Uses,Production

Description

Cinnamic aldehyde is used as a flavoring agent, ingredient of fragrance in soft drinks, ice creams, dentifrices, pastries, chewing-gum, etc. It can induce both contact urticaria and delayed-type reactions. It can be implicated in contact dermatitis in those who work in the perfume industry or food handlers. Cinnamic aldehyde is contained in the "fragrance mix".

Chemical Properties

Cinnamaldehyde exists as yellowish to greenish-yellow oily liquid with a Strong pungent, spicy, cinnamon odor. It is normally insoluble in water and many organic solvents but is miscible with alcohol and other flavoring oils. Exposure to air will result in thickening and oxidation.
Cinnamaldehyde
Cinnamaldehyde (cinnamic aldehyde, benzylideneactaldehyde, phenylacrolein, 3-phenylpropenal, 3-phenyl-2-propenal) is a saturated aldehyde with an aromatic ring that is a yellowish, oily liquid at room temperature. It is used as a flavoring and aromatic agent in a variety of food products, perfumes, and household products. It has also seen use as a rubber reinforcing agent. A burning taste that produces the odor and flavor of the spice may be found with this aromatic aldehyde. Cinnamaldehyde has also been used as an attractant for insect control, in the preparation of corrosion inhibitors, and as a coating for metals. Although extensively used in industry, it is also a natural constituent of cinnamon leaves and bark, some essential oils, and other plant products.

Occurrence

Reported found in celery seed, cinnamon, cinnamon leaf, cassia leaf, clove stem and lemon balm.

Uses

Cinnamic aldehyde is a common ingredient in perfumes for household products like deodorizers, detergents, and soap; flavor in toothpaste, sweets, ice cream, soft drinks, chewing gums, and cakes; in balsam of Tolu and Peru, hyacinth plant, spices, cinnamon, Ceylon and cassia oil; some perfumery uses (Canoe; hyacinth; bubblegum; Balsam; Cassia); natural occurrence (cinnamon).

Uses

Cinnamaldehyde is used in flavor and perfumes.It occurs in cinnamon oils.

Uses

In the flavor and perfume industry.

Definition

ChEBI: (E)-cinnamaldehyde is the E (trans) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes. It has a role as a hypoglycemic agent, an EC 4.3.1.24 (phenylalanine ammonia-lyase) inhibitor, a vasodilator agent, an antifungal agent, a flavouring agent, a plant metabolite and a sensitiser. It is a 3-phenylprop-2-enal and a member of cinnamaldehydes.

Aroma threshold values

Detection at 50 to 750 ppb.

Taste threshold values

Taste characteristics at 0.5 ppm: spicy, cinnamon and cinnamon bark.

General Description

Yellow oily liquid with a cinnamon odor and sweet taste.

Air & Water Reactions

Thickens on exposure to air. May be unstable to prolonged exposure to air. Slightly water soluble .

Reactivity Profile

Cinnamaldehyde reacts with sodium hydroxide owing to aerobic oxidation.

Health Hazard

Cinnamaldehyde can cause moderate to severeskin irritation. Exposure to 40 mg in48 hours produced a severe irritation effecton human skin. The toxicity of this compoundwas low to moderate on test subjects,depending on the species and the toxicroutes. However, when given by oral routein large amounts, its poisoning effect wassevere. Amounts greater than 1500 mg/kghave produced a wide range of toxic effectsin rats, mice, and guinea pigs. The symptomswere respiratory stimulation, somnolence,convulsion, ataxia, coma, hypermotility, anddiarrhea.
LD50 value, oral (guinea pigs): 1150 mg/kg
Cinnamaldehyde is a mutagen. Its carcinogeniceffect is not established.

Fire Hazard

Cinnamaldehyde is combustible.

Agricultural Uses

Fungicide, 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.

Trade name

ADIOS®; ZIMTALDEHYDE®; ZIMTALDEHYDE® LIGHT

Contact allergens

This perfumed molecule is used as a fragrance in perfumes, a flavoring agent in soft drinks, ice creams, dentifrices, pastries, chewing-gum, etc. It can induce both contact urticaria and delayed-type reactions. It can be responsible for dermatitis in the perfume industry or in food handlers. Cinnamic aldehyde is contained in “fragrance mix.” As a fragrance allergen, it has to be mentioned by name in cosmetics within the EU.

Anticancer Research

This is promising in antitumor activity against NSCLC cells. The cells were inducedin apoptosis and also the epithelial-mesenchymal transition was reversed affectingthe Wnt/b-catenin pathway (Bouyahya et al. 2016).

Safety Profile

Poison by intravenous and parenteral routes. Moderately toxic by ingestion and intraperitoneal routes. A severe human skin irritant. Mutation data reported. Combustible liquid. May ipte after a delay period in contact with NaOH. When heated to decomposition it emits acrid smoke and fumes. See also ALDEHYDES.

Synthesis

By isolation from natural sources; synthetically, by condensation of benzaldehyde with acetaldehyde in the presence of sodium or calcium hydroxide.

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.

26958-41-8
104-55-2
Synthesis of Cinnamaldehyde from 1,3-Dithiane, 2-(2-phenylethenyl)-
Global( 709)Suppliers
Supplier Tel Email Country ProdList Advantage
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763 info@tnjchem.com China 2989 55
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17368 58
Shanghai Nuo Rui Hua New Material Technology Co., Ltd
+86-15631980363 +86-15631980363 mandy@sfinechem.com China 99 58
Mainchem Co., Ltd.
-- sarah@mainchem.com China 6572 58
Henan Bao Enluo International TradeCo.,LTD
+86-17331933971 +86-17331933971 deasea125996@gmail.com China 2504 58
Shandong Juchuang Chemical Co., LTD
+86-18885615001 +86-18885615001 admin@juchuangchem.com China 387 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21703 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9359 55

Related articles

  • Synthesis and Uses of Cinnamaldehyde
  • Cinnamaldehyde is a pale yellow gelatinous liquid and an organic compound, which is responsible for the taste and smell of the....
  • Nov 28,2019

View Lastest Price from Cinnamaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cinnamaldehyde pictures 2024-03-19 Cinnamaldehyde
104-55-2
US $3990.00-3975.00 / Tons 1Tons 99.99% 100Tons Hebei Dangtong Import and export Co LTD
Cinnamaldehyde pictures 2024-03-19 Cinnamaldehyde
104-55-2
US $5.00 / KG 1KG ≥98% 200mt/year Jinan Finer Chemical Co., Ltd
Cinnamaldehyde Cinnamic Aldehyde pictures 2024-03-11 Cinnamaldehyde Cinnamic Aldehyde
104-55-2
US $10.00-3.00 / kg 500kg 99.9 200tons Shandong Juchuang Chemical Co., LTD
  • Cinnamaldehyde pictures
  • Cinnamaldehyde
    104-55-2
  • US $3990.00-3975.00 / Tons
  • 99.99%
  • Hebei Dangtong Import and export Co LTD
  • Cinnamaldehyde pictures
  • Cinnamaldehyde
    104-55-2
  • US $5.00 / KG
  • ≥98%
  • Jinan Finer Chemical Co., Ltd
abionca Acrolein, 3-phenyl- Aldehyd skoricovy aldehydskoricovy Benzylideneacetaldehyde beta-phenylacrolein beta-phenylcrolein (E)-3-phenylprop-2-enal Cinnaldehyd CINNAMIC ALDEHYDE, NATURAL Cinnamaldehyde, synthesis grade Cinnamaldehyde 500mg [104-55-2] Cinnamaldehyde,3-Phenylprop-2-enal Ciamaldehyde Cinnamaldehide CINNAMALDEHYDE FOR SYNTHESIS 5 ML CINNAMALDEHYDE FOR SYNTHESIS 250 ML CINNAMALDEHYDE FOR SYNTHESIS 1 L AKOS B004060 AKOS BBS-00003207 CINNAMALDEHYDE CINNAMALDEHYDE, TRANS- LABOTEST-BB LT00939010 TRANS-3-PHENYL-2-PROPEN-1-AL TRANS-3-PHENYL-2-PROPENAL TRANS-ALPHA CINNAMALDEHYDE TRANS-CINNAMIC ALDEHYDE TRANS-CINNAMAL TRANS-PHENYLACROLEIN TRANS-PHENYLACRYLALDEHYDE 3-Fenylpropenal Cassia aldehyde cassiaaldehyde Cinnaldehyde cinnamaldehyde (3-phenyl-2-propenal) cinnamylaldehyde femanumber2286. NCI-C56111 Zimtaldehyde Zimtaldehyd Cininamaldehyde CINNAMALDEHYDE 98+% FCC CINNAMALDEHYDE 93+% NATURAL CinnamicAcidForSynthesis CinnamaldehydeForSynthesis CINNAMIC ALDEHYDE FCC & KOSHER TRANS-CINNAMALDEHYDE,REAGENT Rou Guiquan Cinnamic aldehyde,cinnamaldehyde,β-phenylacrolein  Cinnamaldehyde Vetec(TM) reagent grade, 93% trans-Cinnamaldehyde 3-Phenyl-2-propenal trans-Cinnamaldehyde for synthesis 3-phenyl-2-propena 3-Phenyl-2-propenaldehyde 3-phenyl-acrolei 3-Phenylacrolein Abion CA Cinnamaldehyde 104-55-2