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Merck
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I12603

Sigma-Aldrich

β-Ionone

96%

Sinonimo/i:

beta-Ionone, 4-(2,6,6-Trimethyl-1-cyclohexenyl)-3-buten-2-one

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About This Item

Formula empirica (notazione di Hill):
C13H20O
Numero CAS:
14901-07-6
Peso molecolare:
192.30
Beilstein:
1909544
Numero CE:
201-224-3
Numero MDL:
MFCD00001549
Codice UNSPSC:
12352100
ID PubChem:
24895924
NACRES:
NA.22

Saggio

96%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.52 (lit.)

P. eboll.

126-128 °C/12 mmHg (lit.)

Densità

0.945 g/mL at 25 °C (lit.)

Stringa SMILE

CC(=O)\C=C\C1=C(C)CCCC1(C)C

InChI

1S/C13H20O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h7-8H,5-6,9H2,1-4H3/b8-7+
PSQYTAPXSHCGMF-BQYQJAHWSA-N

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Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H315,H411

Classi di pericolo

Aquatic Chronic 2 - Skin Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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Sigma-Aldrich

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Sigma-Aldrich

Sigma-Aldrich

8.04778

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Sigma-Aldrich

CDS005151

alpha-cyclociral

Damascenone natural, 1.1-1.4 wt. % (190 proof ethanol), FG

Sigma-Aldrich

W342017

Damascenone

A Vieira et al.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 44(6), 538-545 (2011-03-30)
β-ionone (βI), a cyclic isoprenoid, and geraniol (GO), an acyclic monoterpene, represent a promising class of dietary chemopreventive agents against cancer, whose combination could result in synergistic anticarcinogenic effects. The chemopreventive activities of βI and GO were evaluated individually or
Jianfeng Wang et al.
Investigative ophthalmology & visual science, 53(10), 6355-6369 (2012-08-18)
In human retinal degeneration, rod photoreceptors reactively sprout neurites. The mechanism is unknown in part because of the paucity of animal models displaying this feature of human pathology. We tested the role of cAMP and opsin in sprouting by tiger
Shu Wei et al.
Environmental entomology, 40(6), 1622-1630 (2012-01-06)
Plant carotenoid derived β-ionone has been shown to have diverse biological effects on some insect herbivores and herbivore parasitoids. In this study, Arabidopsis transgenic plants over-expressing a carotenoid cleavage dioxygenase1 gene (AtCCD1) were generated to test whether β-ionone emissions could
Mun-Ock Kim et al.
Molecular cancer therapeutics, 9(4), 833-843 (2010-04-01)
beta-Ionone (ION), an end-ring analogue of beta-carotenoid, has been known to inhibit tumor cell growth and induce apoptosis in various types of cancer cells. Nevertheless, its apoptosis-related molecular mechanisms remain unclear. Here, we first investigated the molecular mechanisms by which
Hiroki Irieda et al.
Biochemistry, 50(22), 4912-4922 (2011-05-07)
Organisms sense and respond to environmental stimuli through membrane-embedded receptors and transducers. Sensory rhodopsin I (SRI) and sensory rhodopsin II (SRII) are the photoreceptors for the positive and negative phototaxis in microorganisms, respectively. They form signaling complexes in the membrane
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