EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes

dillapiol (dill)

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CAS Number: 484-31-1Picture of molecule3D/inchi
Nikkaji Web:J12.531H
Beilstein Number:0196037
XlogP3-AA:2.70 (est)
Molecular Weight:222.24038000
Formula:C12 H14 O4
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
Physical Properties:
Appearance:colorless viscous liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:1.16440 @ 0.00 °C.
Refractive Index:1.53050 @ 0.00 °C.
Melting Point: 28.00 to 29.00 °C. @ 760.00 mm Hg
Boiling Point: 285.00 to 292.00 °C. @ 760.00 mm Hg
Boiling Point: 160.00 to 161.00 °C. @ 10.00 mm Hg
Vapor Pressure:0.006000 mmHg @ 25.00 °C. (est)
Flash Point: 222.00 °F. TCC ( 105.70 °C. ) (est)
logP (o/w): 2.343 (est)
Soluble in:
 water, 27.68 mg/L @ 25 °C (est)
Insoluble in:
Organoleptic Properties:
Odor Type: woody
woody spicy
Odor Description:wood spice
Odor and/or flavor descriptions from others (if found).
Cosmetic Information:
None found
BOC Sciences
For experimental / research use only.
For experimental / research use only.
Dillapiole (GC) ≥99%
Safety Information:
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-mouse LD50 1000 mg/kg
Indian Journal of Pharmacy. Vol. 34, Pg. 69, 1972.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Safety in Use Information:
natural substances and extractives
Recommendation for dillapiol (dill) usage levels up to:
 not for fragrance use.
Recommendation for dillapiol (dill) flavor usage levels up to:
 not for flavor use.
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :10231
National Institute of Allergy and Infectious Diseases:Data
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10231
Pubchem (sid):134975341
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
KEGG (GenomeNet):C10449
HMDB (The Human Metabolome Database):HMDB30725
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
Potential Blenders and core components note
None Found
Potential Uses:
None Found
Occurrence (nature, food, other):note
 coriander seed oil
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 coriander seed oil cuba @ 0.45%
Data GC Search Trop Picture
 crithmum maritimum oil @ <0.10%
Data GC Search Trop Picture
 cubeb oil @ 0.16%
Data GC Search Trop Picture
 cumin seed
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 dill leaf
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 dill leaf oil
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 dill oil
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 dill plant
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 dill root oil
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 dill seed
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 dill shoot oil
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 dill weed oil cuba @ 0.31%
Data GC Search Trop Picture
 fennel root oil
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 fennel sprout
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 parsley fruit oil
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 parsley seed oil
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 pepper spiked pepper
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 piper marginatum
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 salvia leucantha
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 trachyspermum roxburghianum benth. ex. kurz. seed oil india @ 0.20%
Data GC Search Trop Picture
1-allyl-2,3-dimethoxy-4,5-(methylene dioxy) benzene
 apiole (dill)
 benzene, 1-allyl-2,3-dimethoxy-4,5-(methylenedioxy)-
1,3-benzodioxole, 4,5-dimethoxy-6-(2-propen-1-yl)-
1,3-benzodioxole, 4,5-dimethoxy-6-(2-propenyl)-
 dill apiole (dill)
1,2-methylene dioxy-5,6-dimethoxy-4-allyl benzene


PubMed:[Chemical constituents of Osmanthus fragrans fruits].
PubMed:Dillapiol: a pyrethrum synergist for control of the Colorado potato beetle.
PubMed:Genetic toxicity of dillapiol and spinosad larvicides in somatic cells of Drosophila melanogaster.
PubMed:Chemical composition and antifungal activity of essential oils and supercritical CO2 extracts of Apium nodiflorum (L.) Lag.
PubMed:The volatile constituents of Salvia leucantha.
PubMed:HIV-1-inhibiting activity of the essential oil of Ridolfia segetum and Oenanthe crocata.
PubMed:Bioactivities of Piper aduncum L. and Piper obliquum Ruiz & Pavon (Piperaceae) essential oils from Eastern Ecuador.
PubMed:Potential control of Aedes aegypti (Diptera: Culicidae) with Piper aduncum L. (Piperaceae) extracts demonstrated by chromosomal biomarkers and toxic effects on interphase nuclei.
PubMed:A synthetic derivative of plant allylpolyalkoxybenzenes induces selective loss of motile cilia in sea urchin embryos.
PubMed:Ciliogenesis, ciliary function, and selective isolation.
PubMed:Modulation of human cytochrome P450 3A4 (CYP3A4) and P-glycoprotein (P-gp) in Caco-2 cell monolayers by selected commercial-source milk thistle and goldenseal products.
PubMed:Dillapiol and Apiol as specific inhibitors of the biosynthesis of aflatoxin G1 in Aspergillus parasiticus.
PubMed:Phytochemistry and antifungal properties of the newly discovered tree Pleodendron costaricense.
PubMed:Evaluation of the efficacy of dill apiol and pyriproxyfen in the treatment and control of Xenopsylla cheopis flea Roths (Siphonaptera: Pulicidae).
PubMed:Traditionally-used antimalarials from the Meliaceae.
PubMed:Antimicrobial constituents of Foeniculum vulgare.
PubMed:An in vitro evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures.
PubMed:Evaluation of anti-inflammatory-related activity of essential oils from the leaves and resin of species of Protium.
PubMed:Genetic analysis of nothoapiol formation in Perilla frutescens.
PubMed:Insecticidal defenses of Piperaceae from the neotropics.
PubMed:Five new prenylated p-hydroxybenzoic acid derivatives with antimicrobial and molluscicidal activity from Piper aduncum leaves.
PubMed:Isolation of dillapiol from a chemotype of Perilla frutescens as an active principle for prolonging hexobarbital-induced sleep.
isolated from perilla frutenscens. Constit. of Japanese, Indian (Anethum sowa) and European (Anethum graveolens) dill oils and Piper spp. Also from seeds of Bunium persicum (black caraway) Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though can be found in a variety of other plants.
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