SMILES string
COc1c(CC=C)cc2OCOc2c1OC
InChI key
LIKYNOPXHGPMIH-UHFFFAOYSA-N
InChI
1S/C12H14O4/c1-4-5-8-6-9-11(16-7-15-9)12(14-3)10(8)13-2/h4,6H,1,5,7H2,2-3H3
grade
analytical standard
assay
≥95.0% (GC)
shelf life
limited shelf life, expiry date on the label
refractive index
n20/D 1.530-1.532
density
1.163 g/mL at 20 °C (lit.)
application(s)
cleaning products
cosmetics
food and beverages
personal care
format
neat
storage temp.
2-8°C
Quality Level
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General description
Dillapiole, a natural constituent of Anethum sowa Roxb, and plant-based insecticide synergist is obtained from Piperaceae, Piper aduncum L. It exhibits potential biological properties, and the essential oil extracted from Piper aduncum L., rich in dillapiole content, is commercially available as an alternative for the natural production of synergistic lignans.
Application
Dillapiole may be used as an analytical reference standard for the quantification of the analyte in French bean Phaseolus sp. treated with pesticidal formulation, dill, caraway seeds and pharmaceutical formulations using chromatography techniques.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Synergistic potential of dillapiole-rich essential oil with synthetic pyrethroid insecticides against fall armyworm
Fazolin M, et al.
Ciencia Rural, 46(3), 382-388 (2016)
Densitometric HPTLC Methods for Qualitative and Quantitative Analysis of Carvone, Dillapiole, Methylparaben and Propylparaben in Dill, Caraway seeds and Pharmaceutical Formulations Utilizing Normal and Reversed-Phase Silica Gel Plates
Alam P, et al.
FABAD Journal of Pharmaceutical Sciences, 38(1), 33-48 (2013)
Dillapiole as antileishmanial agent: discovery, cytotoxic activity and preliminary SAR studies of dillapiole analogues
Parise-Filho R, et al.
Arch. Pharm. (Weinheim), 345(12), 934-944 (2012)
Liquid chromatographic method for the analysis of two plant based insecticide synergists dillapiole and dihydrodillapiole
Walia S, et al.
Journal of Chromatography A, 1047(2), 229-233 (2004)
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