W285609
α-水芹烯
≥75%, stabilized
别名:
2-甲基-5-（1-甲基乙基）-1，3-环己二烯
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关于此项目
经验公式（希尔记法）:
C10H16
化学文摘社编号:
分子量:
136.23
FEMA Number:
2856
Council of Europe no.:
2117
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
1.006
EC Number:
202-792-5
NACRES:
NA.21
MDL number:
Organoleptic:
spicy; woody
Grade:
Halal
Kosher
Kosher
Biological source:
synthetic
Food allergen:
no known allergens
产品名称
α-水芹烯, ≥75%, stabilized
SMILES string
CC(C)C1CC=C(C)C=C1
InChI
1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4-6,8,10H,7H2,1-3H3
InChI key
OGLDWXZKYODSOB-UHFFFAOYSA-N
biological source
synthetic
grade
Halal
Kosher
reg. compliance
FDA 21 CFR 172.515
assay
≥75%
optical activity
[α]20/D −139 to −110°, neat
contains
alpha-tocopherol as additive
refractive index
n20/D 1.474 (lit.)
density
0.85 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
spicy; woody
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Application
- 绿色意味着清洁吗？常规清洁产品与绿色清洁产品的挥发性有机物排放研究。：研究比较了常规清洁产品和绿色清洁产品中的挥发性有机化合物（VOC）排放，确定a-水芹烯是一种常见成分。研究结果强调了绿色产品的环境影响及其有效性（Harding-Smith et al., 2024）。
- 基于RNA-Seq的转录组学和GC-MS定量分析的黄皮种子精油抗白色念珠菌机制研究。：研究使用RNA-Seq和GC-MS研究含有a-水芹烯的黄皮精油对白色念珠菌的抗真菌特性，为其潜在的治疗应用提供见解（Ma et al., 2023）。
- 马钱精油抗霍乱和糖尿病肾保护活性化合物研究：计算和分子动力学研究。本研究确定a-水芹烯是马钱精油中具有抗霍乱和肾脏保护作用的活性化合物，表明其具有治疗霍乱和预防糖尿病肾损伤的潜力（Dahab et al., 2023）。
- 云斑天牛对黄连木挥发性物质的电生理和行为反应。：研究考察了云斑天牛对来自黄连木的a-水芹烯等挥发性物质的反应。这些发现对使用天然挥发物的病虫害管理策略具有启示意义（Fan et al., 2023）。
Disclaimer
仅供R&D或非EU食品使用不用于零售。
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
116.6 °F - closed cup
flash_point_c
47 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Kazuhiro Okamoto et al.
Organic letters, 10(19), 4387-4389 (2008-09-06)
Chiral dienes possessing the bicyclo[2.2.2]octadiene framework were prepared readily through the [4 + 2] cycloaddition of ( R)-alpha-phellandrene with methyl propiolate as the key step. Diene 9, substituted with a tertiary alcohol on one of the two double bonds, is
S Foss et al.
Systematic and applied microbiology, 21(2), 237-244 (1998-08-15)
Four pseudomonad strains 51Men, 54Pin, 62Car and 65Phen were recently isolated on the monoterpenes (+)-menthene, alpha-pinene, 2-carene and alpha-phellandrene as sole carbon source and nitrate as electron acceptor. These bacteria were characterised. The motile, mesophilic, Gram-negative rods had a strictly
Gökalp İşcan et al.
Chemistry & biodiversity, 9(8), 1525-1532 (2012-08-18)
Terpene derivatives converted by microbial biotransformation constitute an important resource for natural pharmaceutical, fragrance, and aroma substances. In the present study, the monoterpene α-phellandrene was biotransformed by 16 different strains of microorganisms (bacteria, fungi, and yeasts). The transformation metabolites were
Huai-sheng Hu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(1), 67-70 (2009-05-19)
The chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus were studied. The essential oil was extracted from the stem of A. brachypus by steam distillation, and its antimicrobial activity was tested in vitro. The chemical constituents
M Miyazawa et al.
Journal of agricultural and food chemistry, 48(7), 2893-2895 (2000-07-18)
gamma-Terpinene was mixed in artificial diet at a concentration of 1 mg/g of diet, and the diet was fed to the last instar larvae of common cutworm (Spodoptera litura). Metabolites were recovered from frass and analyzed spectroscopically. gamma-Terpinene was transformed
实验方案
-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene
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