W259411
α-紫罗兰酮
natural, ≥86%
别名:
4-(2,6,6-三甲基-2-环己烯基)-3-丁烯-2-酮
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关于此项目
经验公式（希尔记法）:
C13H20O
化学文摘社编号:
分子量:
192.30
FEMA编号:
2594
Beilstein:
3197885
EC 号:
欧洲委员会编号:
141
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
7.007
NACRES:
NA.21
等级
Halal
Kosher
natural
质量水平
管理合规性
FDA 21 CFR 117
方案
≥86%
折射率
n20/D 1.498 (lit.)
沸点
259-263 °C (lit.)
密度
0.93 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
floral
SMILES字符串
CC(=O)\C=C\C1C(C)=CCCC1(C)C
InChI
1S/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
UZFLPKAIBPNNCA-BQYQJAHWSA-N
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警示用语：
Danger
危险声明
预防措施声明
危险分类
Resp. Sens. 1
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
244.4 °F - closed cup
闪点(°C)
118 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Stephanie B A de Beer et al.
Journal of chemical information and modeling, 52(8), 2139-2148 (2012-07-07)
Previously, stereoselective hydroxylation of α-ionone by Cytochrome P450 BM3 mutants M01 A82W and M11 L437N was observed. While both mutants hydroxylate α-ionone in a regioselective manner at the C3 position, M01 A82W catalyzes formation of trans-3-OH-α-ionone products whereas M11 L437N
Hao Cai et al.
Molecules (Basel, Switzerland), 18(2), 1368-1382 (2013-01-26)
Flos Lonicerae Japonicae (FLJ) is a popular herb used for many centuries in Traditional Chinese Medicine as a treatment of fever and inflammation. Non-fumigated processing of FLJ has been the traditional approach used in post-harvest preparation of the commodity for
Darunee Soorukram et al.
Organic letters, 6(14), 2409-2411 (2004-07-02)
[reaction: see text] The allylic substitution of sterically hindered (2-iodocycloalkyl)phosphates proceeds with complete anti S(N)2' stereoselectivity with mixed diorganozincs of the type RZnCH(2)SiMe(3) in the presence of CuCN.2LiCl. Only the group R of the copper-zinc reagent is transferred in the
Marco Luparia et al.
Chemistry & biodiversity, 5(6), 1045-1057 (2008-07-12)
To study the influence of the steric bulk of the substituents at C(5) on the olfactory characteristics of alpha-ionone, the (S)-antipodes of compounds 8-10 were synthesized starting from (S)-alpha-cyclogeraniol (14a). The latter was available in useful preparative yield with 95%
S Lutz-Wahl et al.
Applied and environmental microbiology, 64(10), 3878-3881 (1998-10-06)
A total of 215 Streptomyces strains were screened for their capacity to regio- and stereoselectively hydroxylate beta- and/or alpha-ionone to the respective 3-hydroxy derivatives. With beta-ionone as the substrate, 15 strains showed little conversion to 4-hydroxy- and none showed conversion
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