Botanical species · safety record

Petroselinum crispum

The EFSA Compendium of Botanicals holds 36 constituent measurements for Petroselinum crispum. This page reports what those source records contain and how to reach them. It carries no effect estimate, no dose and no recommendation.

Accepted name in source: Petroselinum crispum (Mill.) Fuss

36Constituent measurements
0Safety records
9Cited sources
576Licensed products (Canada)

Also recorded as

Synonyms are carried from the source compendium. A species may be traded and studied under more than one name, which is exactly how a safety record gets lost.

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 576 licensed products naming Petroselinum crispum as a medicinal ingredient, matched on the exact Latin binomial. A licence records that a product met the regulator's requirements for sale in Canada. It is not evidence that the product works.

Extract types on licence

  • Dry
  • Extract Type TBA
  • Fresh

Source material stated

  • Aerial parts
  • Fresh root(s)
  • Grass(es)
  • Herb
  • Herb top
  • Herb top and root
  • Herb(s)
  • Leaf

What the records describe

Constituents measured

  • Furanocoumarins11
  • Bergapten5
  • Isopimpinellin4
  • Psoralen4
  • Myristicin2
  • Nitrate2
  • Apiole1
  • Bergamottin1
  • Bergaptol1
  • Coumarins1

Plant parts

  • Leaves15
  • Live plants9
  • Aerial part of plants7
  • Unspecified3
  • Seed2

Preparations

  • Solvent extraction32
  • Essential oil4

Recorded constituents

What analytical work has found in this species, at which plant part and preparation. A measured constituent is a fact about material, not about effect.

SubstancePlant partPreparationConcentrationAnalytical methodSource
ApioleLeavesEssential oil24.3 PercentUnspecifiedResolve DOI
BergamottinAerial part of plantsSolvent extraction57.9 Nanogram/gramUHPLC-MS-MSResolve DOI
BergaptenLive plantsSolvent extraction≤ 1.7 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
BergaptenAerial part of plantsSolvent extraction11049.3 Nanogram/gramUHPLC-MS-MSResolve DOI
BergaptenLeavesSolvent extraction≤ 146.7 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
BergaptenLeavesSolvent extraction≥ 56.7 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
BergaptenLive plantsSolvent extraction≥ 0.2 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
BergaptolAerial part of plantsSolvent extraction740.4 Nanogram/gramUHPLC-MS-MSResolve DOI
CoumarinsUnspecifiedSolvent extraction37 Microgram/millilitreNuclear Magnetic Resonance (NMR)Resolve DOI
FuranocoumarinsAerial part of plantsSolvent extraction23214.8 Nanogram/gramUHPLC-MS-MSResolve DOI
FuranocoumarinsAerial part of plantsSolvent extraction5971.5 Nanogram/gramUHPLC-MS-MSResolve DOI
FuranocoumarinsLive plantsSolvent extraction≥ 0.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLive plantsSolvent extraction≤ 2.4 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsAerial part of plantsSolvent extraction5971.5 Nanogram/gramUHPLC-MS-MSResolve DOI
FuranocoumarinsLive plantsSolvent extraction≥ 0.1 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLeavesSolvent extraction≤ 53 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLive plantsSolvent extraction≤ 0.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLeavesSolvent extraction≥ 94.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLeavesSolvent extraction≤ 304.4 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FuranocoumarinsLeavesSolvent extraction≥ 5.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
IsopimpinellinLeavesSolvent extraction≥ 15.7 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
IsopimpinellinLive plantsSolvent extraction≤ 0.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
IsopimpinellinLive plantsSolvent extraction≥ 0.1 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
IsopimpinellinLeavesSolvent extraction≤ 79.8 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
MyrceneSeedEssential oil4.25 PercentGC-MSResolve DOI
MyristicinSeedEssential oil42.65 PercentGC-MSResolve DOI
MyristicinLeavesEssential oilStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
OxypeucedaninLeavesSolvent extractionNuclear Magnetic Resonance (NMR)Resolve DOI
Oxypeucedanin hydrateLeavesSolvent extractionNuclear Magnetic Resonance (NMR)Resolve DOI
PabulenolLeavesSolvent extractionNuclear Magnetic Resonance (NMR)Resolve DOI
PsoralenLeavesSolvent extraction≥ 32.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
PsoralenLeavesSolvent extraction≤ 104.7 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
PsoralenLive plantsSolvent extraction< 0.1 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
PsoralenAerial part of plantsSolvent extraction5386 Nanogram/gramUHPLC-MS-MSResolve DOI
NitrateUnspecifiedSolvent extraction≥ 674 Milligram/kilogramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
NitrateUnspecifiedSolvent extraction≤ 1588 Milligram/kilogramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier

Cited sources

The literature the compendium cites for this species. Metatron Health has no relationship with these authors or journals and earns nothing from citing them.

  1. BEIER, RC., IVIE, GW., OERTLI, EH. LINEAR FURANOCOUMARINS AND GRAVEOLONE FROM THE COMMON HERB PARSLEY. Phytochemistry, 1994, vol. 36, no. 4, p. 869-872. DOI
  2. Peroutka, Radek., Schulzova, Vera., Botek, Petr., Hajslova, Jana. Analysis of furanocoumarins in vegetables (Apiaceae) anal citrus fruits (Rutaceae). JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2007, vol. 87, no. 11, p. 2152-2163. DOI
  3. Melough, Melissa M., Lee, Sang Gil., Cho, Eunyoung., Kim, Kijoon., Provatas, Anthony A., Perkins, Christopher., Park, Min Kyung., Quresh, Abrar., Chun, Ock K. Identification and Quantitation of Furocoumarins in Popularly Consumed Foods in the US Using QuEChERS Extraction Coupled with UPLC-MS/MS Analysis . Journal of agricultural and food chemistry, 2017, vol. 65, no. 24, p. 5049-5055. DOI
  4. Ojala, T., Vuorela, P., Kiviranta, J., Vuorela, H., Hiltunen, R. A bioassay using Artemia salina for detecting phototoxicity of plant coumarins . Planta medica, 1999, vol. 65, no. 8, p. 715-718. DOI
  5. Sousa, Rose Marie O. F., Rosa, Jose S., Oliveira, Luisa., Cunha, Ana., Fernandes-Ferreira, Manuel. Activities of Apiaceae essential oils and volatile compounds on hatchability, development, reproduction and nutrition of Pseudaletia unipuncta (Lepidoptera: Noctuidae) . Industrial crops and products, 2015, vol. 63, p. 226-237. DOI
  6. Sbai, Haifa., Saad, Ines., Ghezal, Nadia., Della Greca, Marina., Haouala, Rabiaa. Bioactive compounds isolated from Petroselinum crispum L. leaves using bioguided fractionation . Industrial crops and products, 2016, vol. 89, p. 207-214. DOI
  7. Tamme, T., Reinik, M., Roasto, M., Juhkam, K., Tenno, T., Kiis, A. Nitrates and nitrites in vegetables and vegetable-based products and their intakes by the Estonian population. Food additives & contaminants, 2006, vol. 23, no. 4, p. 355-361.
  8. Mahmoodi, Leila., Valizadegan, Oroj., Mahdavi, Vahid. Fumigant toxicity of Petroselinum crispum L. (Apiaceae) essential oil on Trialeurodes vaporariorum (Westwood) (Hemiptera: Aleyrodidae) adults under greenhouse conditions . Journal of plant protection research, 2014, vol. 54, no. 3, p. 294-299. DOI
  9. ZHENG, GQ., KENNEY, PM., ZHANG, JL., LAM, LKT. INHIBITION OF BENZO A PYRENE-INDUCED TUMORIGENESIS BY MYRISTICIN, A VOLATILE AROMA CONSTITUENT OF PARSLEY LEAF OIL . Carcinogenesis, 1992, vol. 13, no. 10, p. 1921-1923. DOI

Boundary

A constituent measurement is a fact about material at a stated preparation, not a statement about what that material does in a person. An adverse-effect or genotoxicity record is an observation reported in a source, most often in an animal or laboratory model. Neither is a Metatron Health conclusion about causality, human risk or benefit, and the absence of a record is not proof that a preparation is safe. Nothing here is diagnosis, prescribing or individual medical care.

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