α-Isomethyl ionone

α-Isomethyl ionone
Names
IUPAC name
(3E)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one
Other names
α-Cetone
Cetone Alpha
Isomethyl-α-ionone
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.407
EC Number
  • 204-846-3
UNII
  • InChI=1S/C14H22O/c1-10-7-6-8-14(4,5)13(10)9-11(2)12(3)15/h7,9,13H,6,8H2,1-5H3/b11-9+
    Key: JRJBVWJSTHECJK-PKNBQFBNSA-N
  • CC(=O)C(\C)=C\C1C(C)=CCCC1(C)C
Properties
C14H22O
Molar mass 206.3239
Appearance liquid
Density 0.93 gcm −3 (20 °C)
Boiling point 93 °C (199 °F; 366 K) (3.1 mmHg)[1]
0.064 g/L
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
irritant, environmental hazard
GHS labelling:
Warning
H315, H317, H319, H411, H412
P261, P264, P272, P273, P280, P302+P352, P305+P351+P338, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

α-Isomethyl ionone, also known as α-cetone, is a synthetically made and naturally occurring organic compound found in Brewer's yeasts or the species known as Saccharomyces cerevisiae. The compound is an isomer of methyl ionone. Alpha-isomethyl ionone can be colorless or pale-straw coloured liquid. Its primary scent is flowery and secondary scent is violet. It may also have a woody or orris-like scent. and is often used in flavouring and cosmetic industries for example, aftershave lotions, bath products, hair care products, moisturizers, perfumes, shampoos and skin care products. It is also an ingredient used in Chanel No. 5, and other branded products such as Fidji by Guy Laroche. Perfume fragrances that α-isomethyl ionone is used in are for example, amber, chypre, violet, mimosa, reseda, iris, orris, cyclamen, chypre, berries, woody notes, ylang-ylang, leather, orange, nut, pistachio, muscatel, and tobacco.