所有图片(1)
About This Item
经验公式（希尔记法）:
C10H16
CAS号:
分子量:
136.23
FEMA编号:
2856
EC 号:
欧洲委员会编号:
2117
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
1.006
NACRES:
NA.21
性状检查:
spicy; woody
等级:
Halal
Kosher
Kosher
生物来源:
synthetic
食品过敏原:
no known allergens
推荐产品
生物来源
synthetic
质量水平
等级
Halal
Kosher
管理合规性
FDA 21 CFR 172.515
方案
≥75%
旋光性
[α]20/D −139 to −110°, neat
包含
alpha-tocopherol as additive
折射率
n20/D 1.474 (lit.)
密度
0.85 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
spicy; woody
SMILES字符串
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
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应用
- 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）。
免责声明
仅供R&D或非EU食品使用不用于零售。
警示用语：
Danger
危险声明
危险分类
Asp. Tox. 1 - Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
116.6 °F - closed cup
闪点(°C)
47 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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
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
David F Lima et al.
The Journal of pharmacy and pharmacology, 64(2), 283-292 (2012-01-10)
The aim of this work was to investigate the antinociceptive property of α-phellandrene (α-PHE) in experimental nociception models and possible mechanisms involved. Mass spectrometry was used to evaluate the purity and molecular mass of α-PHE. Macrophages from mice peritoneal cavity
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
实验方案
-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene
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