Botanical species · safety record

Melaleuca cajuputi

The EFSA Compendium of Botanicals holds 10 constituent measurements for Melaleuca cajuputi. 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: Melaleuca cajuputi Powell

10Constituent measurements
0Safety records
5Cited sources
45Licensed 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 45 licensed products naming Melaleuca cajuputi 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.

Source material stated

  • Essential oil from leaf
  • Fresh leaves
  • Leaf
  • Leaf/Leaves
  • Leaves
  • Melaleuca cajuputi - Twig Leafy
  • Twig leafy
  • Twigs

What the records describe

Constituents measured

  • 1,8-cineole4
  • Eugenol2
  • Methyleugenol2
  • Myrcene1
  • Tannins1

Plant parts

  • Leaves7
  • Live plants2
  • Stem1
  • stalk1

Preparations

  • Essential oil5
  • Solvent extraction5

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
1,8-cineoleLeavesEssential oil43.7 PercentGC-MSResolve DOI
TanninsStem / stalkSolvent extraction98.8 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
1,8-cineoleLeavesEssential oil≤ 60.2 PercentGaschromatography (GC)No resolvable identifier
1,8-cineoleLive plantsEssential oil65.2 PercentUnspecifiedNo resolvable identifier
1,8-cineoleLeavesEssential oil≥ 42.7 PercentGaschromatography (GC)No resolvable identifier
EugenolLeavesSolvent extraction≥ 0.4 PercentGC-FIDNo resolvable identifier
EugenolLeavesSolvent extraction≤ 1.2 PercentGC-FIDNo resolvable identifier
MethyleugenolLeavesSolvent extraction≥ 0.2 PercentGC-FIDNo resolvable identifier
MethyleugenolLeavesSolvent extraction≤ 1.3 PercentGC-FIDNo resolvable identifier
MyrceneLive plantsEssential oil0.9 PercentUnspecifiedNo 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. Susanto, M., Doran, J., Arnold, R., Rimbawanto, A. Genetic variation in growth and oil characteristics of Melaleuca cajuputi subsp cajuputi and potential for genetic improvement . Journal of tropical forest science, 2003, vol. 15, no. 3, p. 469-482.
  2. Silva, Cleber J., Barbosa, Luiz C. A., Maltha, Ulia R. A., Pinheiro, Antonio L., Ismail, Fyaz M. D. Comparative study of the essential oils of seven Meialeuca (Myrtaceae) species grown in Brazil. FLAVOUR AND FRAGRANCE JOURNAL, 2007, vol. 22, no. 6, p. 474-478. DOI
  3. Galle-Hoffmann, Ute., Konig, Wilfried A. Essential oils. Part 3. Additional tea tree oils from Melaleuca. Deutsche apotheker zeitung, 1999, p. 59-62.
  4. Jajaei, S. M., Daud, W. R. W., Markom, M., Zakaria, Z., Lo Presti, M., Costa, Rosaria., Mondello, L., Santi, Luca. Extraction of Melaleuca cajuputi Using Supercritical Fluid Extraction and Solvent Extraction. JOURNAL OF ESSENTIAL OIL RESEARCH, 2010, vol. 22, no. 3, p. 205-210.
  5. Batubara, I., Kotsuka, S., Yamauchi, K., Kuspradini, H., Mitsunaga, T., Darusman, L.K. TNF-alpha production inhibitory activity, phenolic, flavonoid and tannin contents of selected Indonesian medicinal plants. Research Journal of Medicinal Plant, 2012, vol. 6, no. 6, p. 406-415. 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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