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α-Ionone

(3E)-4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-buten-2-one

Parmone · 4,7-Megastigmadien-9-one

Monocyclic monoterpenoid alkene ketone · C₁₃H₂₀O

Chemical structure of α-Ionone
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
24190-29-2
Molecular formula
C₁₃H₂₀O
Molecular weight
192.30 g/mol
Aroma
Defining violet, soft and sweet, with woody undertones.

Safety

Low concern · Safe at standard use

α-Ionone is the principal constituent of violet aroma in perfumery. It occurs at low levels in osmanthus and champaca absolutes.

Skin. Patch tests on 25 volunteers with undiluted ionone (a mixture of α and β) caused no irritation, and at 8 percent no sensitization. A 48-hour patch test at 32 percent in acetone caused moderate irritation. In 100 consecutive dermatitis patients, no reactions occurred at 1 percent.

Oral. Acute oral LD50 in mice is 6.6 to 7.0 g/kg.

Subchronic. A 90-day study at 10 or 100 mg/kg/day established a NOAEL of 10 mg/kg. In another 12-week study the NOAEL was 10.6 mg/kg.

Mutagenicity. Not mutagenic in the Ames test, weakly genotoxic in Chinese hamster cells, not genotoxic in micronucleus tests.


Usage guidelines

Concern level
Low
90-day NOAEL
10 mg/kg/day
Oils with high content
Osmanthus absolute, Orange champaca absolute

Found in essential oils

Principal sources
Osmanthustr – 2.3 %
Champaca (orange)0.1 – 1.6 %

Pharmacokinetics

α-Ionone metabolism involves oxidation, reduction and glucuronide conjugation. The compound induces CYP1A and CYP2B.


Notes

α-Ionone and β-ionone are the ionone pair responsible for violet aroma, produced synthetically at large scale for perfumery. Natural ionone is rare and precious, found mainly in osmanthus.