General Information of Natural Product (ID: NP0713)
  Natural Product Name
2,2,6-Trimethylcyclohexanone
  Synonyms
2,2,6-TRIMETHYLCYCLOHEXANONE; 2408-37-9; 2,2,6-Trimethylcyclohexan-1-one; Cyclohexanone, 2,2,6-trimethyl-; 2,6,6-Trimethylcyclohexanone; 1,1,3-Trimethyl-2-cyclohexanone; (+/-)-2,2,6-Trimethylcyclohexanone; FEMA No. 3473; 2,6,6-Trimethylcyclohexan-1-one; cistus cyclohexanone; EINECS 219-309-9; NSC401659; NSC 401659; 2,6-Trimethylcyclohexanone; Cyclohexanone,2,6-trimethyl-; SCHEMBL107630; 1,3-Trimethyl-2-cyclohexanone; 2,2,6-Trimethyl cyclohexanone; 2,2,6-trimethyl-cyclohexanone; 2,6-Trimethylcyclohexan-1-one; DTXSID20862925; 2,2,6-trimethyl-cyclohexan-1-one; AMY38174; MFCD00045550; AKOS015903247; HY-W077671; NSC-401659; AS-44336; DB-046342; CS-0113167; FT-0634253; J-015344; Q27275646
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  Formula C9H16O
  Weight 140.22
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C9H16O/c1-7-5-4-6-9(2,3)8(7)10/h7H,4-6H2,1-3H3
  InChI Key ZPVOLGVTNLDBFI-UHFFFAOYSA-N
  Isomeric SMILES CC1CCCC(C1=O)(C)C
  Canonical SMILES CC1CCCC(C1=O)(C)C
  External Links PubChem ID 17000
CAS ID 2408-37-9

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Cistus ladanifer
  Factor Name: Locality Variation [1]
              Species Info Factor Info
               Experiment Detail
Cistus ladanifer was collected from two sites, in July-August 2001, after the flowering season. The major quantity was brought from the wild, where the plant was growing in the mountainous region of the center-interior of the country (site 1). A smaller amount was harvested from a cultivated plant in the north of Portugal (site 2) that was propagated from a wild plant found in the dry plain region in the South of Portugal.
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               Factor Function
Considering the oil composition of cistus plants from different sites, there were found some differences. The cistus oil of site 2 had a high content on the ocimenone isomers, an absence of trans-pinocarveol and unknown (compound 17) and a higher quantity of less volatile compounds such as sclareol oxide and 15-nor-labdan-8-ol. Cistus oil from site 1 was richer in sesquiterpene alcohols and 2,2,6-trimethylcyclohexanone. The amount of ambrox was the same for both oils. Considering the use of fresh or dry plant, the composition of cistus from site 2 was more affected, decreasing the amount of components of middle to high volatility and increasing the amount of the less volatiles. Drying promoted the doubling of the amount of ocimenone isomers in cistus oil from site 2 and of unknown (compound 21) and sesquiperpene alcohol (compound 29) in cistus from site 1. Again the quantity of ambrox was the same for both oils.
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               Factor Part Location NP Content
 
Fresh plant: (Locality: center-interior of Portugal)
Leaves and branches Portugal
NP Content: 2 %
 
Fresh plant: (Locality: north of Portugal)
Leaves and branches Portugal
NP Content: 0.3 %
 
Dry plant: (Locality: center-interior of Portugal)
Leaves and branches Portugal
NP Content: 2.8 %
References
1 Characterization of the Portuguese-Grown Cistus ladanifer Essential Oil