General Information of Natural Product (ID: NP0194)
  Natural Product Name
Ethyl Dodecanoate
  Synonyms
ETHYL LAURATE; Ethyl dodecanoate; 106-33-2; Dodecanoic acid, ethyl ester; Lauric acid ethyl ester; Ethyl laurinate; Ethyl dodecylate; Lauric acid, ethyl ester; dodecanoic acid ethyl ester; Ethyl n-dodecanote; UNII-F389D4MD5K; MFCD00015065; Ethyl n-dodecanoate; F389D4MD5K; CHEBI:87427; Lauric acid, ethyl ester (8CI); DODECANOIC ACID,ETHYL ESTER; WE(2:0/12:0); Ethyl laurate (natural); FEMA No. 2441; EINECS 203-386-0; NSC 83467; AI3-00645; Dodecanoic acid ethyl; dodecanoic acid-ethyl ester; Ethyl ester dodecanoic acid; SCHEMBL8538; DSSTox_CID_27044; DSSTox_RID_82065; NCIOpen2_004797; DSSTox_GSID_47044; Ethyl ester of dodecanoic acid; CHEMBL3187842; DTXSID4047044; Ethyl Laurate(Ethyl Dodecanoate); FEMA 2441; NSC8912; Ethyl laurate, analytical standard; NSC-8912; NSC83467; ZINC1648325; Tox21_300967; LMFA07010464; NSC-83467; Ethyl laurate, >=98%, FCC, FG; AKOS009157278; Ethyl dodecanoate, >=98.0% (GC); MCULE-6150658986; NCGC00248234-01; NCGC00254870-01; BS-14294; CAS-106-33-2; SY037739; Ethyl laurate, natural, >=98%, FCC, FG; FT-0625573; L0013; V0948; D70267; A934209; Ethyl dodecanoate, Vetec(TM) reagent grade, 98%; J-001577; Q18023029; F8889-6672; Ethyl laurate, United States Pharmacopeia (USP) Reference Standard
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  Formula C14H28O2
  Weight 228.37
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-12-13-14(15)16-4-2/h3-13H2,1-2H3
  InChI Key MMXKVMNBHPAILY-UHFFFAOYSA-N
  Isomeric SMILES CCCCCCCCCCCC(=O)OCC
  Canonical SMILES CCCCCCCCCCCC(=O)OCC
  External Links PubChem ID 7800
CAS ID 106-33-2
NPASS ID NPC250028
CHEMBL ID CHEMBL3187842
  NP Activity Charts   Click to show/hide

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Vitis vinifera
  Factor Name: Variety Comparison [1]
              Species Info Factor Info
               Experiment Detail
Grape pomaces and stalks of Nero d'Avola and Frappato were donated by the ''Valle dell'Acate'' wine firm, Acate, RG, Italy - those from Nerello Mascalese and Cabernet Sauvignon were given by the ''Emanuele Scammacca Barone del Murgo'' wine firm, Santa Venerina, CT, Italy. The winemaking procedures were similar for all samples, namely grape clusters were crushed and destemmed using a destemmer-crusher. The crushed grapes were treated with sulphur dioxide (0.2-0.5% total mash) and with selected strains of Saccharomyces cerevisiae to start up the fermentation. After 6-8 days of maceration, when alcoholic fermentation was finished, the mash was pressed. Stalks coming from destemming procedure and grape pomace coming from the maceration procedure were subjected to the distillation procedures within 24 h of their collection. All materials were collected during the 2004 vintage.
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               Factor Function
On the whole, 38 components have been characterized in the samples of grape pomaces, with Frappato cv. showing the richest composition; instead, 88 components have been detected in the stalks of Frappato, Nero d'Avola, Nerello Mascalese and Cabernet Sauvignon varieties.
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               Factor Part Location NP Content
 
Vitis vinifera var. Cabernet Sauvignon
Pomaces Italy
NP Content: 6.01 %
 
Vitis vinifera var. Cabernet Sauvignon
Stalks Italy
NP Content: < 0.05 %
 
Vitis vinifera var. Frappato
Pomaces Italy
NP Content: 10.01 %
 
Vitis vinifera var. Nerello Mascalese
Pomaces Italy
NP Content: 14.67 %
 
Vitis vinifera var. Nero d'Avola
Pomaces Italy
NP Content: 15.38 %
 
Vitis vinifera var. Nero d'Avola
Stalks Italy
NP Content: < 0.05 %
References
1 Volatile components of grape pomaces from different cultivars of Sicilian Vitis vinifera L.