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Catalogue Number
BD-D0412
Analysis Method
HPLC,NMR,MS
Specification
HPLC≥90%
Storage
2-8°C
Molecular Weight
220.4
Appearance
Powder
Botanical Source
Structure Type
Sesquiterpenoids
Category
Standards;Natural Pytochemical;API
SMILES
CC(C)C1CCC(C(C1=O)C(=C)C)(C)C=C
Synonyms
Mcneil 1025/NORBORMIDE/Nobormide/Shoxin/Caswell No. 606/Cyclohexanone, 3-ethenyl-3-methyl-2-(1-methylethenyl)-6-(1-methylethyl)-, (2S,3S,6S)-/(2S,3S,6S)-2-Isopropenyl-6-isopropyl-3-methyl-3-vinylcyclohexanone/Compound S-6,999
IUPAC Name
(2S,3S,6S)-3-ethenyl-3-methyl-6-propan-2-yl-2-prop-1-en-2-ylcyclohexan-1-one
Applications
Density
0.9±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
116.2±22.0 °C
Boiling Point
290.2±39.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C15H24O/c1-7-15(6)9-8-12(10(2)3)14(16)13(15)11(4)5/h7,10,12-13H,1,4,8-9H2,2-3,5-6H3/t12-,13+,15+/m0/s1
InChl Key
GWHRSRIPLDHJHR-GZBFAFLISA-N
WGK Germany
RID/ADR
HS Code Reference
2914290000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:21698-44-2) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
26600710
CONTEXT:
It was found that the essential oil of Acorus calamus rhizomes showed insecticidal activity.
AIM:
The aim of this study was to determine the chemical composition of the essential oil from A. calamus rhizomes, evaluate insecticidal and repellant activity against Lasioderma serricorne (LS) and Tribolium castaneum (TC), and to isolate any insecticidal constituents from the essential oil.
MATERIALS AND METHODS:
Essential oil from A. calamus was obtained by hydrodistillation and analyzed by gas chromatography (GC) flame ionization detector and GC-mass spectrometry. The insecticidal and repellant activity of the essential oil and isolated compounds was tested using a variety of methods.
RESULTS:
The main components of the essential oil were identified to be isoshyobunone (15.56%), β-asarone (10.03%), bicyclo[6.1.0]non-1-ene (9.67%), shyobunone (9.60%) and methylisoeugenol (6.69%). Among them, the two active constituents were isolated and identified as shyobunone and isoshyobunone. The essential oil showed contact toxicity against LS and TC with LD50 values of 14.40 and 32.55 μg/adult, respectively. The isolated compounds, shyobunone and isoshyobunone also exhibited strong contact toxicity against LS adults with LD50 values of 20.24 and 24.19 μg/adult, respectively, while the LD50 value of isoshyobunone was 61.90 μg/adult for TC adults. The essential oil, shyobunone and isoshyobunone were strongly repellent (98%, 90% and 94%, respectively, at 78.63 nL/cm(2), after 2 h treatment) against TC.
CONCLUSION:
The essential oil, shyobunone and isoshyobunone possessed insecticidal and repellant activity against LS and TC.
Acorus calamus; Lasioderma serricorne; Tribolium castaneum; contact toxicity; repellency
Repellant and insecticidal activities of shyobunone and isoshyobunone derived from the essential oil of Acorus calamus rhizomes.
Chen HP1, Yang K2, Zheng LS1, You CX2, Cai Q1, Wang CF3.
2015 Oct-Dec
