Zimtaldehyd

Cinnamaldehyde Struktur
104-55-2
CAS-Nr.
104-55-2
Bezeichnung:
Zimtaldehyd
Englisch Name:
Cinnamaldehyde
Synonyma:
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
Summenformel:
C9H8O
Molgewicht:
132.16
MOL-Datei:
104-55-2.mol

Zimtaldehyd Eigenschaften

Schmelzpunkt:
−9-−4 °C(lit.)
Siedepunkt:
248 °C (lit.)
Dichte
1.05 g/mL at 25 °C (lit.)
Dampfdichte
4.6 (vs air)
Dampfdruck
<0.1 hPa (20 °C)
FEMA 
2286 | CINNAMALDEHYDE
Brechungsindex
n20/D 1.622(lit.)
Flammpunkt:
160 °F
storage temp. 
Store below +30°C.
Löslichkeit
1g/l soluble
Aggregatzustand
Liquid
pka
0[at 20 ℃]
Farbe
Clear yellow
Wichte
1.05
Geruch (Odor)
Strong odor of cinnamon
Geruchsart
spicy
Wasserlöslichkeit
Slightly soluble
Merck 
13,2319
JECFA Number
656
Dielectric constant
16.9(24℃)
Stabilität:
Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
InChIKey
KJPRLNWUNMBNBZ-QPJJXVBHSA-N
LogP
1.83-2.1 at 25-27℃
CAS Datenbank
104-55-2(CAS DataBase Reference)
NIST chemische Informationen
Cinnamylaldehyde(104-55-2)
EPA chemische Informationen
Cinnamaldehyde (104-55-2)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 36/37/38-43
S-Sätze: 26-36/37
RIDADR  UN8027
WGK Germany  3
RTECS-Nr. GD6476000
10-23
HS Code  29122900
Giftige Stoffe Daten 104-55-2(Hazardous Substances Data)
Toxizität LD50 in rats (mg/kg): 2220 orally (Jenner)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P271 Nur im Freien oder in gut belüfteten Räumen verwenden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.

Zimtaldehyd Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R43:Sensibilisierung durch Hautkontakt möglich.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.

Beschreibung

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".

Chemische Eigenschaften

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.

Verwenden

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

Allgemeine Beschreibung

Yellow oily liquid with a cinnamon odor and sweet taste.

Air & Water Reaktionen

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

Reaktivität anzeigen

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.

Brandgefahr

Cinnamaldehyde is combustible.

Landwirtschaftliche Anwendung

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.

Handelsname

ADIOS®; ZIMTALDEHYDE®; ZIMTALDEHYDE® LIGHT

Kontakt-Allergie

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).

Sicherheitsprofil

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.

mögliche Exposition

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.

Versand/Shipping

UN1989 Aldehydes, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid

Inkompatibilitäten

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.

Zimtaldehyd Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Zimtaldehyd Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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104-55-2(Zimtaldehyd)Verwandte Suche:


  • 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
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