W329304
α-当归内酯
98%, FG
别名:
4-羟基-3-戊烯酸-γ-内酯, 5-甲基-2(3H)-呋喃酮
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关于此项目
经验公式（希尔记法）:
C5H6O2
CAS Number:
分子量:
98.10
FEMA编号:
3293
Beilstein:
108394
EC 号:
欧洲委员会编号:
731
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
10.012
NACRES:
NA.21
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
meets purity specifications of JECFA
生物来源
synthetic
等级
FG
Fragrance grade
Halal
Kosher
Agency
follows IFRA guidelines
meets purity specifications of JECFA
管理合规性
EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
方案
98%
折射率
n20/D 1.448 (lit.)
沸点
55-56 °C/12 mmHg (lit.)
mp
13-17 °C (lit.)
密度
1.092 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
致敏芳香化合物
no known allergens
性状检查
coconut; oily; sweet
SMILES字符串
CC1=CCC(=O)O1
InChI
1S/C5H6O2/c1-4-2-3-5(6)7-4/h2H,3H2,1H3
InChI key
QOTQFLOTGBBMEX-UHFFFAOYSA-N
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一般描述
α-Angelica lactone, a cyclic lactone that occurs naturally in tobacco, is generally used in tobacco flavoring.
包装
玻璃瓶包装
警示用语：
Warning
危险声明
危险分类
Skin Sens. 1
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
154.4 °F - closed cup
闪点(°C)
68 °C - closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Chemical composition and carcinogenicity of smokeless tobacco.
Hoffmann D & Djordjevic MV.
Advances in Dental Research, 11(3), 322-329 (1997)
Efficient conversion of ?-angelica lactone into ?-valerolactone with ionic liquids at room temperature
Cao R, et al.
ACS sustainable chemistry & engineering, 2(4), 902-909 (2014)
Y M Ioannou et al.
Cancer research, 42(4), 1199-1204 (1982-04-01)
The effects of alpha-angelica lactone (alpha-AL), butylated hydroxyanisole (BHA), and beta-naphthoflavone (beta-NF) on the amount of benzo(alpha)pyrene (BP) metabolite:DNA adducts formed in the forestomach, lung, and liver of ICR/Ha mice were investigated 48 hr after p.o. administration of BP. BP
W A Nijhoff et al.
Carcinogenesis, 16(3), 607-612 (1995-03-01)
The naturally occurring anticarcinogens flavone and alpha-angelicalactone incorporated separately and simultaneously in the diet at 0.5, 0.1, 0.05 and 0.01% w/w, were studied with respect to their effects on oesophageal, gastric, intestinal, colonic and hepatic (i) glutathione S-transferase (GST) enzyme
Xin Huang et al.
Chemical communications (Cambridge, England), 48(18), 2439-2441 (2012-01-24)
The first organocatalytic asymmetric assembly of Morita-Baylis-Hillman carbonates of isatins and α-angelica lactone has been studied, affording multifunctional products containing two valuable pharmacophores and vicinal quaternary chiral centers in high stereoselectivity (up to 92% ee, dr >95:5).
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