35031-06-2 Usage
Description
(Z)-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one, commonly known as alpha-Ionone, is a chemical compound classified under the enones category. It is a colorless to pale yellow liquid with a distinct floral and woody odor. (Z)-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one is naturally present in a range of plants, such as roses, violets, and various fruits, and is valued for its diverse applications.
Uses
Used in Fragrance Industry:
Alpha-Ionone is utilized as a key component in the fragrance industry due to its violet-like scent. Its ability to impart a pleasant and distinctive aroma makes it a popular choice for creating various perfumes and colognes.
Used in Flavor Industry:
In addition to its use in fragrances, alpha-Ionone is also employed as a flavoring agent in the food products sector. Its unique taste and aroma enhance the sensory experience of various consumables, contributing to the overall appeal of the product.
Used in Pharmaceutical Research:
(Z)-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one has been investigated for its potential biological activities, which include anti-inflammatory and antioxidant properties. This research suggests that alpha-Ionone may have therapeutic applications in the future, particularly in the development of treatments for inflammation-related conditions and those that could benefit from its antioxidant effects.
Check Digit Verification of cas no
The CAS Registry Mumber 35031-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35031-06:
(7*3)+(6*5)+(5*0)+(4*3)+(3*1)+(2*0)+(1*6)=72
72 % 10 = 2
So 35031-06-2 is a valid CAS Registry Number.
35031-06-2Relevant articles and documents
PHOTOCHEMISTRY OF DIENONES-VIII; THE LOW TEMPERATURE PHOTOCHEMISTRY OF (Z)-β-IONONE AND ITS PHOTO-ISOMERS
Cerfontain, Hans,Geenevasen, Jan A. J.
, p. 1571 - 1576 (2007/10/02)
The isomerizations of (E)-β-ionone 1, and of mixtures of the isomeric pyran 2 and (Z)-β-ionone 3 in CD3OD as solvent on direct irradiation with λ 254 nm and on triplet photo-sensitization have been studied at temperatures 24:Φ34=0.50.On starting with either 1 or mixtures of 2 and 3 the same photo-stationary equilibrium ratio of 1-3 is eventually obtained, viz 1:2:3=17:72:11. 4 is photostable relative to 1-3.The perdeuterobenzophenone triplet photo-sensitization with λ 366 nm at -50 deg C of 1 leads to 3 as the sole primary product, which isomer on triplet sensitization yields both 1 and 2.The triplet sensitized conversion is much faster for (Z)- than (E)-β-ionone.On starting with either 1 or mixtures of 2 and 3, eventually the same photo-stationary state is obtained, viz 1:2:3=39:46:15. (Z)-retro-γ-ionone 4 is not formed in the triplet sensitized irradiations of 1, 2 and 3 and in the direct irradiation it apparently results from the singlet excited state of the three substrates.The UV spectrum of the (unstable) (Z)-β-ionone 3 has been indirectly determined; its absorption occurs at lower wavelength and is of lower intensity than that of the (E)-isomer 1.
