eucalyptus polybractea extract
blue-leaved mallee extract
Identification
| Name | eucalyptus polybractea extract |
| IUPAC | eucalyptus polybractea extract |
| CAS Number | 91771-67-4 |
| FDA UNII | Search |
Regulatory
Physical Properties
| Food Chemicals Codex Listed | No |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for eucalyptus polybractea extract usage levels up to | not for fragrance use. |
| Recommendation for eucalyptus polybractea extract flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
blue-leaved mallee extract
PubMed:
Native Australian species are effective in extracting multiple heavy metals from biosolids.
PubMed:
Localization of oleuropeyl glucose esters and a flavanone to secretory cavities of Myrtaceae.
PubMed:
Multiphoton fluorescence lifetime imaging shows spatial segregation of secondary metabolites in Eucalyptus secretory cavities.
PubMed:
Validation of models to estimate the fumigant and larvicidal activity of Eucalyptus essential oils against Aedes aegypti (Diptera: Culicidae).
PubMed:
Chemical composition and fumigant toxicity of the essential oils from 16 species of Eucalyptus against Haematobia irritans (Diptera: Muscidae) adults.
PubMed:
The influence of micropropagation on growth and coppicing ability of Eucalyptus polybractea.
PubMed:
Regulation of oil accumulation in single glands of Eucalyptus polybractea.
PubMed:
Fumigant activity of plant essential oils and components from garlic (Allium sativum) and clove bud (Eugenia caryophyllata) oils against the Japanese termite (Reticulitermes speratus Kolbe).
PubMed:
Roles of cytochrome P450 3A enzymes in the 2-hydroxylation of 1,4-cineole, a monoterpene cyclic ether, by rat and human liver microsomes.
PubMed:
Oxidation of 1,8-cineole, the monoterpene cyclic ether originated from eucalyptus polybractea, by cytochrome P450 3A enzymes in rat and human liver microsomes.