General Information of Natural Product (ID: NP1960)
  Natural Product Name
Myrtenal + Myrtenol
  Synonyms
Myrtenal; 564-94-3; (1R)-(-)-Myrtenal; D-myrtenal; Benihinal; (+)-Myrtenal; (1S)-Myrtenal; 2-Norpinene-2-carboxaldehyde, 6,6-dimethyl-; Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-; 2-Formyl-6,6-dimethylbicyclo(3.1.1)hept-2-ene; Pin-2-ene-1-carbaldehyde; BICYCLO(3.1.1)HEPT-2-ENE-2-CARBOXALDEHYDE, 6,6-DIMETHYL-; 6,6-Dimethyl-2-norpinene-2-carboxaldehyde; 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde; (1S,5R)-(+)-6,6-Dimethyl-2-norpinene-2-carboxaldehyde; (1S)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carboxaldehyde; (1S,5R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carboxaldehyde; 6,6-Dimethylbicyclo(3.1.1)hept-2-ene-2-carboxaldehyde; (1R)-2-Pinen-10-al; (1r)-(-) myrtenal; 2-Norpinene-2-carboxaldehyde, 6,6-dimethyl- (8CI); bmse000534; (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-carboxaldehyde; SCHEMBL228374; Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-, (1S)-; FEMA 3395; NSC54384; BICYCLO[3.1.1]HEPT-2-ENE-2-CARBOXALDEHYDE,6,6-DIMETHYL-; AKOS000120250; LMPR0102120023; MCULE-6569061785; 2-Norpinene-2-carboxaldehyde,6-dimethyl-; DB-065494; CS-0081952; J-011849; Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6-dimethyl-; 6,6-Dimethyl-bicyclo [3.1.1]hept-2-ene-2-carbaldehyde; 6,6-Dimethyl-bicyclo[3,1,1]hept-2-ene-2-carboxaldehyde; 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde #
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  Formula C10H14O
  Weight 150.22
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C10H14O/c1-10(2)8-4-3-7(6-11)9(10)5-8/h3,6,8-9H,4-5H2,1-2H3
  InChI Key KMRMUZKLFIEVAO-UHFFFAOYSA-N
  Isomeric SMILES CC1(C2CC=C(C1C2)C=O)C
  Canonical SMILES CC1(C2CC=C(C1C2)C=O)C
  External Links PubChem ID 61130
CAS ID 564-94-3
HIT ID C0609

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Lavandula latifolia
  Factor Name: Developmental Stage Variation [1]
              Species Info Factor Info
               Experiment Detail
Plant material: Samples of L. latifolia were collected in August 1998 during the full flowering period (L/La) and in October 1998 during the fruiting period (L/Lb) from three different spike lavender populations located into the Cazorla, Segura y Las Villas Natural Park (Jaen province, Spain). The plant material from each population consisted of the twigs of several single plants. L/La (Location: 'Garganta de Hornos', Altitude (m): 950, Harvesting date: August 14, 1998, Phenological stage: Flowering); L/Lb (Location: 'Garganta de Hornos', Altitude (m): 950, Harvesting date: October 15, 1998, Phenological stage: Fruiting).
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               Factor Function
The small amounts of linalool needed to match the standard can be reached in a natural way (from full flowering to fruiting) which means it is important to choose the most convenient time of harvest in the studied area.
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               Factor Part Location NP Content
 
Whole plant: Flowering stage
Whole plant Spain
NP Content: 0.3 %
 
Whole plant:Fruiting stage
Whole plant Spain
NP Content: 0.3 %
References
1 Chemical Composition and Seasonal Variations of Spike Lavender Oil from Southern Spain