Details of Natural Product (NP)

General Information of Natural Product (ID: NP1954)
  Natural Product Name
Limonene + Eucalyptol
  Synonyms
LIMONENE; Dipentene; 138-86-3; Cinene; Cajeputene; DL-Limonene; Kautschin; p-Mentha-1,8-diene; Dipenten; Eulimen; Nesol; 1,8-p-Menthadiene; Cyclohexene, 1-methyl-4-(1-methylethenyl)-; Cajeputen; Limonen; Cinen; Inactive limonene; Acintene DP dipentene; 1-Methyl-4-(1-methylethenyl)cyclohexene; Polylimonene; Dipanol; Unitene; alpha-Limonene; Flavor orange; Orange flavor; Goldflush II; Acintene DP; Di-p-mentha-1,8-diene; 1,8(9)-p-Menthadiene; 4-Isopropenyl-1-methyl-1-cyclohexene; 4-Isopropenyl-1-methylcyclohexene; 1-methyl-4-prop-1-en-2-ylcyclohexene; p-Mentha-1,8-diene, dl-; (+/-)-Limonene; DL-4-Isopropenyl-1-methylcyclohexene; 1-Methyl-4-isopropenyl-1-cyclohexene; MENTHA-1,8-DIENE (DL); Dipentene, technical grade; .alpha.-Limonene; NSC 21446; PC 560; 1-methyl-4-(prop-1-en-2-yl)cyclohex-1-ene; .delta.-1,8-Terpodiene; 7705-14-8; CHEBI:15384; 1-Methyl-4-isopropenylcyclohexene; Limonene, dl-; 65996-98-7; NCGC00163742-03; Polydipentene; Limonene polymer; DSSTox_CID_9612; d,l-Limonene; Dipentene polymer; DSSTox_RID_78787; DSSTox_GSID_29612; Dipentene 200; Terpenes and Terpenoids, limonene fraction; (+-)-Dipentene; (+-)-Linonene; Caswell No. 526; Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (.+/-.)-; delta-1,8-Terpodiene; (+-)-alpha-Limonene; d-Limonene (JAN); Dipentene, crude; CAS-138-86-3; HSDB 1809; NSC 844; p-Mentha-1,8-diene, (+-)-; Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (R)-; EINECS 205-341-0; EINECS 231-732-0; UN2052; 1-Methyl-p-isopropenyl-1-cyclohexene; DIPENTENE (+-); EPA Pesticide Chemical Code 079701; NSC-844; Terpodiene; Ciene; Cyclil decene; AI3-00739; NSC-21446; Achilles dipentene; NSC-757069; Dipentene, tech.; 4-isopropenyl-1-methyl-cyclohexene; Dipentene, technical, for use as solvent (for the paint industry), mixture of various terpenes; c0626; Mentha-1,8-diene; p-Mentha-1, dl-; Dipentene, homopolymer; d(R)-4-Isopropenyl-1-methylcyclohexene; (.+-.)-Limonene; (.+-.)-Dipentene; (.+/-.)-Dipentene; (.+/-.)-Limonene; DIPENTENE 38 PF; Limonene, (+/-)-; ESSENCE DE PIN PF; (1)-1-Methyl-4-(1-methylvinyl)cyclohexene; DL-p-mentha-1,8-diene; Mentha-1,8-diene, DL; (+-)-(RS)-limonene; Cyclohexene, (.+-.)-; Dipentene, p.a., 95%; p-Mentha-1,8(9)-diene; Dipentene, mixture of isomers; CHEMBL15799; Monocyclic terpene hydrocarbons; Methyl-4-isopropenylcyclohexene; NSC844; (.+/-.)-.alpha.-Limonene; DTXSID2029612; (+/-)-p-Mentha-1,8-diene; p-Mentha-1, (.+-.)-; HMS3264E05; Pharmakon1600-00307080; Methyl-4-isopropenyl-1-cyclohexene; HY-N0544; NSC21446; Tox21_112068; Tox21_201818; Tox21_303409; MFCD00062992; NSC757069; STK801934; 1-methyl-4-isopropenylcyclohex-1-ene; AKOS009031280; Cyclohexene, 4-Isopropenyl-1-methyl-; Methyl-4-(1-methylethenyl)cyclohexene; WLN: L6UTJ A1 DY1 & U1; CCG-214016; MCULE-2462317444; p-Mentha-1,8-diene, (.+/-.)-; p-Mentha-1,8-diene, polymers (8CI); SB44847; UN 2052; (+/-)-p-Mentha-1,8-diene homopolymer; Limonene 1000 microg/mL in Isopropanol; NCGC00163742-01; NCGC00163742-02; NCGC00163742-04; NCGC00163742-05; NCGC00257291-01; NCGC00259367-01; Terpenes andTerpenoids, limonene fraction; 8050-32-6; NCI60_041856; p-Mentha-1,8-diene, homopolymer (7CI); 1-methyl-4-(1-methylethenyl) cylcohexene; 1-methyl-4-(prop-1-en-2-yl)cyclohexene; 4-(1-methylethenyl)-1-methyl-cyclohexene; Dipentene [UN2052] [Flammable liquid]; Cyclohexene, 1-methyl-4-(1-methylethynyl); DB-053490; DB-072716; CS-0009072; FT-0600409; FT-0603053; FT-0605227; L0046; EN300-21627; C06078; D00194; 1-METHYL-4-PROP-1-EN-2-YL-CYCLOHEXENE; AB01563249_01; Q278809; SR-01000872759; J-007186; J-520048; SR-01000872759-1; 4B4F06FC-8293-455D-8FD5-C970CDB001EE; Dipentene, mixt. of limonene, 56-64%, and terpinolene, 20-25%; 555-08-8; 8016-20-4; 8022-90-0
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  Formula C10H16
  Weight 136.23
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3
  InChI Key XMGQYMWWDOXHJM-UHFFFAOYSA-N
  Isomeric SMILES CC1=CCC(CC1)C(=C)C
  Canonical SMILES CC1=CCC(CC1)C(=C)C
  External Links PubChem ID 22311
CAS ID 138-86-3
NPASS ID NPC34764
CHEMBL ID CHEMBL15799
  NP Activity Charts   Click to show/hide
  Activity Info  

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Ruta chalepensis
  Factor Name: Developmental Stage Variation [1]
              Species Info Factor Info
               Experiment Detail
Ruta chalepensis seedlings were sown in the field in January 1999. Leaf materials were collected at vegetative stage (25th August 1999, plant height 60 cm, temp. min. 26.4 ℃, max. 35.6 ℃) and at budding stage (25th February 1999, plant height 115 cm, temp. min. 9.6 ℃, ma. 26.2 ℃). At flowering stage (2Sth March 2000, plant height 118 cm, temp. min. 14.3 ℃, max. 29.7 ℃), both leaves and flowers were collected; at fruiting stage (25th April 2000, plant height 119 cm, temp. min. 21.5 ℃, max. 39.1 ℃), leaves and fruits were again collected for oil isolation and analysis.
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               Factor Function
Analysis of the oils from R. chalepensis showed that the major constituents of oils were 2-undecanone, 2-nonanone, 2- nonyl-acetate and 2-dodecanone. 2-Undecanone was found to reach a maximum in the flower oil followed by fruit and leaf oils. The quantity of 2-undecanone was highest in the leaves when the plants were young and in the vegetative stage, and it gradually decreased when the plants started flowering and fruiting. 2-Nonanone, on the other hand, was at its maximum in the Leaf oil followed by flower and fruit oils. The quantity of 2-nonanone in the leaves gradually increased from the vegetative stage to the flowering stage and was highest during fruiting stage. The concentration of 2-nonyl acetate was observed to be highest in the leaves during the vegetative stage, while 2-dodecanone was at its maximum in the fruits. Lina-lool, an important aromatic compound, has been found to be highest in flowers. Gamma-Terpinene and 6-methyl-5-hepten-2-one were observed only in vegetative stage of the plants. During the flowering and fruiting stages they could not be detected. Pregeijerene was observed during flowering only, while geijerene was observed both during flowering and fruiting; however, this compound was found in leaves.
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               Factor Part Location NP Content
 
Fruit: Fruiting Stage
 Fruits Lucknow, India
NP Content: 0.01 %
 
Leaf: Budding Stage
 Leaves Lucknow, India
NP Content: 0.1 %
 
Leaf: Vegetative stage
 Leaves Lucknow, India
NP Content: 0.1 %
 
Leaf: Flowering stage
 Leaves Lucknow, India
NP Content: 0.2 %
 
Leaf: Fruiting Stage
 Leaves Lucknow, India
NP Content: 0.1 %
References
1 Variations in Essential Oil Constituents at Different Growth Stages of Ruta chalepensis on Cultivation at North Indian Plains