DODECYL ACETATE

DODECYL ACETATE Struktur
112-66-3
CAS-Nr.
112-66-3
Englisch Name:
DODECYL ACETATE
Synonyma:
FEMA 2616;NSC 67366;acetatec-12;LAURYLACETAT;Acetate C-12;Dodecylacetat;Okimelanolure;LAURYL ACETATE;DODECYL ACETATE;Dodecylethanoate
CBNumber:
CB1481796
Summenformel:
C14H28O2
Molgewicht:
228.37
MOL-Datei:
112-66-3.mol

DODECYL ACETATE Eigenschaften

Schmelzpunkt:
1.3℃
Siedepunkt:
150 °C15 mm Hg(lit.)
Dichte
0.865 g/mL at 25 °C(lit.)
Brechungsindex
n20/D 1.432(lit.)
FEMA 
2616 | LAURYL ACETATE
Flammpunkt:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
Löslichkeit
Acetone (Slightly), Chloroform (Slightly), Hexanes (Slightly)
Aggregatzustand
Oil
Farbe
Colourless
Geruch (Odor)
at 100.00 %. sweet fresh laundared cloths clean waxy
Geruchsart
waxy
JECFA Number
133
LogP
6.02
CAS Datenbank
112-66-3(CAS DataBase Reference)
EPA chemische Informationen
Acetic acid, dodecyl ester (112-66-3)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
R-Sätze: 53
WGK Germany  2
RTECS-Nr. AH3525000
HS Code  2915.39.4000
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H227 Combustible liquid Flammable liquids Category 4 Warnung P210, P280, P370+P378, P403+P235,P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P370+P378 Bei Brand: zum Löschen verwenden.
P403+P235 An einem gut belüfteten Ort aufbewahren. Kühl halten.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

DODECYL ACETATE Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Lauryl acetate has a characteristic citrus-rose odor. The corre sponding flavor develops only on dilution. May be prepared by acetylation of lauryl alcohol.

Chemische Eigenschaften

Lauryl acetate has a characteristic citrus–rose odor. The corresponding flavor develops only on dilution.

Occurrence

Reported found in sour cherry, cardamom, bitter orange, lime, lemon and mandarin peel oils.

Verwenden

1-Dodecanol Acetate can be used as a foaming agent in the purification process of quartz sand. Furthermore, it is a main component of the essential oil from the flowers of Etlingera elatior (Jack) R. M. Smith, which is found to be active against Staphylococcus aureus, Bacillus cereus, Candida albicans and Cryptococcus neoformans.

synthetische

By acetylation of lauryl alcohol.

DODECYL ACETATE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


DODECYL ACETATE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 149)Lieferanten
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112-66-3()Verwandte Suche:


  • n-dodecylacetate
  • LAURYL ACETATE 98+%
  • Dodecylacetat
  • LAURYLACETAT
  • Lauryl acetate,Dodecyl acetate, Lauryl acetate
  • Dodecylethanoate
  • n-Dodecyl acetate
  • n-Dodecyl ethanoate
  • ACETIC ACID DODECYL ESTER
  • ACETIC ACID LAURYL ESTER
  • ACETIC ACID N-DODECYL ESTER
  • Dodecyl acetate, Lauryl acetate
  • Acetic acid dodecyl
  • DODECYL ACETATE
  • FEMA 2616
  • LAURYL ACETATE
  • 1-Dodecanol acetate
  • Acetic Acid Lauryl Ester Acetic Acid Dodecyl Ester Lauryl Acetate
  • NSC 67366
  • Okimelanolure
  • 1-dodecanolacetate
  • Acetate C-12
  • acetatec-12
  • Dodecan-1-yl acetate
  • dodecan-1-ylacetate
  • Dodecanol acetate
  • dodecanolacetate
  • Dodecanyl acetate
  • Dodecyl alcohol, acetate
  • dodecylalcoholacetate
  • Dodecyl Acetate >
  • DODECYL ACETATE USP/EP/BP
  • 112-66-3
  • CH3COOC12H25
  • 112663
  • CH3CO2CH211CH3
  • Esters
  • Organic Building Blocks
  • Building Blocks
  • C12 to C63
  • Carbonyl Compounds
  • Esters
  • Fatty Acyls
  • Fatty Esters
  • Lipids
  • Organic Building Blocks
  • Alcohol Acetates
  • Biochemicals and Reagents
  • Building Blocks
  • C12 to C63
  • Carbonyl Compounds
  • Chemical Synthesis
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