CAS 127-41-3
:α-Ionone
Description:
α-Ionone is an organic compound classified as a monoterpenoid and is part of the larger family of ionones, which are derived from the degradation of carotenoids. It is characterized by its pleasant floral and woody aroma, making it a popular ingredient in the fragrance and flavor industry. The molecular formula of α-ionone is C13H18O, and it features a cyclohexene ring with a ketone functional group, contributing to its distinctive scent profile. α-Ionone is typically a colorless to pale yellow liquid at room temperature and is soluble in organic solvents but has limited solubility in water. It is known for its stability under normal conditions but can undergo oxidation if exposed to air over time. In addition to its use in perfumes, α-ionone is also utilized in food flavoring and has potential applications in the pharmaceutical industry due to its biological activity. Safety data indicate that it should be handled with care, as it can cause skin irritation and allergic reactions in some individuals.
Formula:C13H20O
InChI:InChI=1/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:InChIKey=UZFLPKAIBPNNCA-BQYQJAHWNA-N
SMILES:C(=C/C(C)=O)\C1C(C)(C)CCC=C1C
Synonyms:- (.+-.)-trans-α-Ionone
- (3E)-4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-buten-2-one
- (3E)-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-one
- (3E)-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one
- (3E)-4-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]but-3-en-2-one
- (3E)-4-[(1S)-2,6,6-trimethylcyclohex-2-en-1-yl]but-3-en-2-one
- (3Z)-4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-one
- (5E)-Ionone
- (E)-4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-buten-2-one
- (E)-α-Ionone
- 3-Buten-2-one, 4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (3E)-
- 3-Buten-2-one, 4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (E)-
- 4-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-3-buten-2-one
- 4-(2,6,6-Trimethyl-2-cyclohexenyl)-3-buten-2-one
- 4-(2,6,6-Trimethylcyclohex-1-En-1-Yl)But-3-En-2-One
- 4-(2,6,6-Trimethylcyclohex-1-Ene-1-Yl)-But-3-Ene-2-One
- 4-(2,6,6-Trimethylcyclohex-2-Ene-1-Yl)-But-3-Ene-2-One
- 4-(2,6,6-Trimethylcyclohex-2-en-1-yl)-but-3-en-2-on
- 4-(2,6,6-Trimethylcyclohex-2-en-1-yl)-but-3-en-2-one
- 4-(2,6,6-Trimetilciclohex-2-Eno-1-Il)-But-3-Eno-2-Ona
- But-3-En-2-One, 4-(2,6,6-Trimethyl-2-Cyclohexen-1-Yl)-, (E)-
- IONONE , α-
- Ionone
- Irisone
- α-Cyclocitrylideneacetone
- See more synonyms
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Found 10 products.
α-Ionone
CAS:alpha-Ionone analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C13H20OPurity:(GC) ≥90%Color and Shape:LiquidMolecular weight:192.33-Buten-2-one, 4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (3E)-
CAS:Formula:C13H20OPurity:80%Color and Shape:LiquidMolecular weight:192.2973α-ionone
CAS:<p>α-ionone</p>Formula:C13H20OPurity:90%Color and Shape: clear. very pale yellow liquidMolecular weight:192.2973g/molα-Ionone
CAS:Formula:C13H20OPurity:(all isomers) ≥ 90.0%Color and Shape:Colourless to light yellow liquidMolecular weight:192.30α-Ionone
CAS:<p>alpha-Ionone is a natural product for research related to life sciences. The catalog number is TN3385 and the CAS number is 127-41-3.</p>Formula:C13H20OPurity:98%Color and Shape:SolidMolecular weight:192.30α-Ionone
CAS:Formula:C13H20OPurity:>90.0%(GC)Color and Shape:Colorless to Yellow clear liquidMolecular weight:192.30α-Ionone (>90%)
CAS:Controlled Product<p>Applications An aroma compound commonly found in essential oils such as rose oil. It is a degradation products of caratenoids produced by caratenoid cleavage dioxygenases (CCD).<br>References Susanne, B. et al.: J. Exp. Botany, 61, 2967 (2010); Hu, H. et al.: Arch. Pham. res., 32, 699 (2009);<br></p>Formula:C13H20OPurity:>90%Color and Shape:Clear ColourlessMolecular weight:192.30a-Ionone
CAS:<p>α-Ionone is a natural compound that belongs to the class of carotenoids. It has been shown to have anti-angiogenic effects and inhibit the proliferation of cancerous cells, such as cervical cancer cells. α-Ionone also inhibits the growth of HL60 cells in vitro and has shown an anti-tumor effect on human leukemia cells. This compound also has odorant binding properties which may be due to its hydroxyl group. α-Ionone can be found in various plants, such as kidney beans and some other legumes, where it is produced by the enzymatic conversion of zeranol. It can also be synthesized from dehydrocostus lactone, sodium citrate, and anhydrous sodium fatty acid.</p>Formula:C13H20OPurity:90%MinColor and Shape:Clear LiquidMolecular weight:192.3 g/mol4-(2,6,6-Trimethylcyclohex-2-en-1-yl)but-3-en-2-one
CAS:Formula:C13H20OPurity:≥90%(GC)(mixture of isomers)Color and Shape:No data available.Molecular weight:192.302









