58170
α-Ionone
technical, ≥90% (GC)
Synonym(s):
4-(2,6,6-Trimethyl-2-cyclohexenyl)-3-buten-2-one
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About This Item
Empirical Formula (Hill Notation):
C13H20O
CAS Number:
Molecular Weight:
192.30
EC Number:
204-841-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3197885
MDL number:
grade
technical
assay
≥90% (GC)
impurities
<10% β-ionone
refractive index
n20/D 1.498 (lit.), n20/D 1.500
bp
259-263 °C (lit.)
density
0.93 g/mL at 25 °C (lit.)
SMILES string
CC(=O)\C=C\C1C(C)=CCCC1(C)C
InChI
1S/C13H20O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h6-8,12H,5,9H2,1-4H3/b8-7+
InChI key
UZFLPKAIBPNNCA-BQYQJAHWSA-N
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Marco Luparia et al.
Chemistry & biodiversity, 5(6), 1045-1057 (2008-07-12)
To study the influence of the steric bulk of the substituents at C(5) on the olfactory characteristics of alpha-ionone, the (S)-antipodes of compounds 8-10 were synthesized starting from (S)-alpha-cyclogeraniol (14a). The latter was available in useful preparative yield with 95%
J Lalko et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45 Suppl 1, S251-S257 (2007-11-23)
A toxicologic and dermatologic review of ionone when used as a fragrance ingredient is presented.
Ufuk Ozgen et al.
Molecules (Basel, Switzerland), 15(4), 2593-2599 (2010-04-30)
Sonchus erzincanicus (Asteraceae) is an endemic species in Turkey, where six Sonchus species grow. In this study, a phytochemical study was performed on the aerial parts of the plant. The study describes the isolation and structure elucidation of five flavonoids
Global Trade Item Number
| SKU | GTIN |
|---|---|
| G0513-25MG | 04061833623978 |
| G0513-100MG | 04061832908632 |