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Supelco

Dillapiole

analytical standard

Synonym(s):

6-Allyl-4,5-dimethoxy-1,3-benzodioxole

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About This Item

Empirical Formula (Hill Notation):
C12H14O4
CAS Number:
Molecular Weight:
222.24
Beilstein:
196037
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

COc1c(CC=C)cc2OCOc2c1OC

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

InChI key

LIKYNOPXHGPMIH-UHFFFAOYSA-N

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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.

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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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)
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)
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)
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)

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