| Identification | Back Directory | [Name]
DILLAPIOLE | [CAS]
484-31-1 | [Synonyms]
dillapiol
DILLAPIOLE
apiole (dill)
DILLAPIOL(SG)
dillapiol (dill)
DILLAPIOLE WITH GC
6-ALLYL-4,5-DIMETHOXY-1,3-BENZODIOXOLE
4,5-Dimethoxy-6-allyl-1,3-benzodioxole
6-Allyl-4,5-dimethoxybenzo[d][1,3]dioxole
4,5-dimethoxy-6-(2-propenyl)-3-benzodioxole
4,5-dimethoxy-6-prop-2-enyl-1,3-benzodioxole
4,5-dimethoxy-6-(2-propenyl)-1,3-benzodioxole
1-Allyl-2,3-dimethoxy-4,5-methylenedioxybenzene
1,3-Benzodioxole, 4,5-dimethoxy-6-(2-propenyl)-
1-allyl-2,3-dimethoxy-4,5-(methylenedioxy)-benzen
1,3-Benzodioxole, 4,5-dimethoxy-6-(2-propen-1-yl)-
Benzene, 1-allyl-2,3-dimethoxy-4,5-(methylenedioxy)-
dillapiol,4,5-dimethoxy-6-(2-propenyl)-1,3-benzodioxole,dillapiol | [Molecular Formula]
C12H14O4 | [MDL Number]
MFCD00210045 | [MOL File]
484-31-1.mol | [Molecular Weight]
222.24 |
| Chemical Properties | Back Directory | [Melting point ]
29.5° | [Boiling point ]
bp 285° | [density ]
1.163 g/mL at 20 °C (lit.) | [refractive index ]
n20/D 1.533 | [storage temp. ]
2-8°C | [Odor]
wood spice | [Odor Type]
woody | [Merck ]
13,740 | [BRN ]
196037 | [LogP]
2.343 (est) |
| Hazard Information | Back Directory | [Uses]
Dillapiol is an organic compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. | [Uses]
Dillapiole may be used as an analytical reference standard for the quantification of the analyte in French bean Pha搜索引擎优化lus sp. treated with pesticidal formulation, dill, caraway seeds and pharmaceutical formulations using chromatography techniques. | [Definition]
ChEBI: Dillapiole is a member of benzodioxoles. It has a role as a metabolite. | [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. |
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