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58220

Sigma-Aldrich

Irone

technical, mixture of isomers (mainly the α-isomer), ≥90% (GC)

Synonym(s):

α-Irone, 4-(2,5,6,6-Tetramethyl-2-cyclohexen-1-yl)-3-buten-2-one, 4-(2,5,6,6-Tetramethyl-2-cyclohexen-1-yl)-3-butene-2-one, 6-Methyl-α-ionone, Methyl-α-ionone

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About This Item

Empirical Formula (Hill Notation):
C14H22O
CAS Number:
79-69-6
Molecular Weight:
206.32
Beilstein:
1343498
EC Number:
201-219-6
MDL number:
MFCD00042628
UNSPSC Code:
12352115
PubChem Substance ID:
57651648
NACRES:
NA.22

grade

technical

Assay

≥90% (GC)

refractive index

n20/D 1.492

density

0.934 g/mL at 20 °C (lit.)

SMILES string

CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C

InChI

1S/C14H22O/c1-10-6-7-11(2)14(4,5)13(10)9-8-12(3)15/h6,8-9,11,13H,7H2,1-5H3/b9-8+

InChI key

JZQOJFLIJNRDHK-CMDGGOBGSA-N

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General description

Irone is a bioactive compound that is produced by an endophytic fungus in the rhizomes of Iris germanica.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J Lalko et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45 Suppl 1, S272-S275 (2007-11-23)
A toxicologic and dermatologic review of alpha-irone when used as a fragrance ingredient is presented.
Endophytic fungi for producing bioactive compounds originally from their host plants.
Zhao J, et al.
Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology, 1, 567-576 (2010)

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