Ethyloctanoat

Ethyl caprylate  Struktur
106-32-1
CAS-Nr.
106-32-1
Bezeichnung:
Ethyloctanoat
Englisch Name:
Ethyl caprylate
Synonyma:
ETHYL OCTANOATE;OCTANOIC ACID ETHYL ESTER;Octanoic acid ethyl;Ethyl octoate;Ethyl carprylate;Ethyloctanoat;ETHYL OCTYLATE;Etheyl Octanoat;WC3035;WC 3035
CBNumber:
CB4852670
Summenformel:
C10H20O2
Molgewicht:
172.26
MOL-Datei:
106-32-1.mol

Ethyloctanoat Eigenschaften

Schmelzpunkt:
-48--47 °C (lit.)
Siedepunkt:
206-208 °C (lit.)
Dichte
0.867 g/mL at 20 °C (lit.)
Dampfdruck
0.02 mm Hg ( 25 °C)
Brechungsindex
n20/D 1.417(lit.)
FEMA 
2449 | ETHYL OCTANOATE
Flammpunkt:
167 °F
storage temp. 
Store below +30°C.
Löslichkeit
ethanol: soluble1ml/4ml, clear, colorless (70% ethanol)
Aggregatzustand
Liquid
Farbe
Clear colorless
Geruch (Odor)
at 100.00 %. fruity wine waxy sweet apricot banana brandy pear
Geruchsart
waxy
Explosionsgrenze
0.7%(V)
Wasserlöslichkeit
insoluble
Merck 
14,3778
JECFA Number
33
BRN 
1754470
LogP
4.47 at 22.7℃
CAS Datenbank
106-32-1(CAS DataBase Reference)
NIST chemische Informationen
Octanoic acid, ethyl ester(106-32-1)
EPA chemische Informationen
Ethyl octanoate (106-32-1)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 38
S-Sätze: 26-36
WGK Germany  2
RTECS-Nr. RH0680000
Selbstentzündungstemperatur 325 °C
TSCA  Yes
HS Code  29159080
Toxizität LD50 orally in rats: 25,960 mg/kg, P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H411 Giftig für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 2
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P391 Verschüttete Mengen aufnehmen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Ethyloctanoat Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R38:Reizt die Haut.

S-Sätze Betriebsanweisung:

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

Beschreibung

Ethyl caprylate (ethyl octanoate) is a kind of fatty acid ester formed from caprylic acid and ethanol. It is a kind of natural fruit flavoring agent. It is usually included in the alcohol beverage. Among the main flavoring components of None-flavor liquor, the absolute content of ethyl caprylate is not high but its flavoring contributions is higher than ethyl acetate, ethyl lactate, and ethyl butyrate, only lower than ethyl caproate. Only small amount of ethyl caprylate could produce obvious fruit aroma in Nong-flavor liquor. However, excessive content of ethyl caprylate would inhibit the performance of other flavoring components.

Chemische Eigenschaften

CLEAR COLOURLESS LIQUID

Occurrence

Reported found in apple, apricot, orange juice, grapefruit juice, guava, pineapple, cheddar cheese, other cheeses, butter, beer, cognac, rum, whiskey, cider, grape wines, cocoa, coconut meat, passion fruit, mango, pawpaw and mastic gum leaf oil.

Verwenden

Ethyl caprylate is a flavoring and fragrance agent.

synthetische

Usually prepared by esterification of caprylic acid with ethyl alcohol and sulfuric acid as catalyst; also by alcoholysis of coconut oil in the presence of HCl.

Definition

ChEBI: A fatty acid ethyl ester resulting from the formal condensation of octanoic acid with ethanol.

Allgemeine Beschreibung

Ethyl octanoate is a powerful odourant found in mead (a traditional drink that contains alcohol).

Sicherheitsprofil

Mddly toxic by ingestion. A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.

Carcinogenicity

Not listed by ACGIH, California Proposition 65, IARC, NTP, or OSHA.

Stoffwechsel

Aliphatic esters including ethyl caprylate are thought to be readily hydrolysed to the corresponding alcohol and acid, which are then further metabolized (Fassett, 1963). Oral adminis tration of ethyl caprylate to rats produced a ketonuria twice as great as that from acetoacetate, indicating the formation of two fragments for the production of ketone bodies, and it was suggested that caprylic acid was probably broken down by a process involving multiple alternate oxidation (Deuel, Hallman, Butts & Murray, 1936).

Einzelnachweise

Powers, John J. "HETEROGENEITY AND TEMPERATURE EFFECTS ON FLAVOR SENSING OF ETHYL CAPRYLATE." Journal of Food Science 42.1(2010):275-276.
Zhibin, L. I., and L. I. Jin. "Analysis of the Content of Ethyl Caprylate in Nong-flavor Liquor and Its Flavoring Contributions." Liquor-Making Science & Technology (2013).

Ethyloctanoat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ethyloctanoat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 388)Lieferanten
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106-32-1(Ethyloctanoat)Verwandte Suche:


  • Ethyl octanoate >=98.0%
  • Ethyl caprylate, synthesis grade
  • Ethyl caprylate, 99+% 5ML
  • CAPRYLIC ACID ETHYLESTER WITH GC
  • ETHYL CAPRYLATE, NATURAL
  • Ethyl octanoate Vetec(TM) reagent grade, 98%
  • Ethyl octanoate ReagentPlus(R), >=99%
  • Ethyl Octlate
  • FEMA 2449
  • ETHYL N-CAPRYLATE
  • ETHYL N-OCTANOATE
  • ETHYL CAPRYLATE
  • CAPRYLIC ACID-ETHYL
  • CAPRYLIC ACID ETHYL ESTER
  • N-OCTANOIC ACID ETHYL ESTER
  • N-CAPRYLIC ACID ETHYL ESTER
  • RARECHEM AL BI 0166
  • ETHYL OCTANOATE 98+% FCC
  • ETHYL CAPRYLATE, 99+%
  • ETHYL OCTANOATE 98+% NATURAL FCC
  • ethyloctanoate,ethylcaprylate
  • CAPRYLIC ACID ETHYLESTER(SG)
  • Natural Ethyl Octanoate
  • Natural Ethyl Caprylate
  • Ethyln-Octanoate>
  • Ethyl caprylate, 99%, for synthesis
  • Ethyl caprylate@10 mg/mL in Hexane
  • éthyl caprylate
  • Ethyl caprylate USP/EP/BP
  • Ethyl octanoate(kosher)
  • WC 3035
  • WC3035
  • WC-3035
  • Octanoic acid ethyl
  • Ethyl carprylate
  • Ethyloctanoat
  • Ethyl octoate
  • ETHYL OCTYLATE
  • ETHYL OCTANOATE
  • OCTANOIC ACID ETHYL ESTER
  • Etheyl Octanoat
  • OCTANOIC ETHYL
  • 106-32-1
  • CH3CH26CO2CH2CH3
  • CH3CH26COOC2H5
  • C10 to C11
  • Carbonyl Compounds
  • Building Blocks
  • Esters
  • Organic Building Blocks
  • Pharmaceutical Intermediates
  • 106-32-1
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