生物来源
synthetic
质量水平
等级
Halal
Kosher
管理合规性
FDA 21 CFR 172.515
检测方案
≥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
- Does green mean clean Volatile organic emissions from regular versus green cleaning products.: This research compares the volatile organic compound (VOC) emissions from conventional and green cleaning products, identifying a-phellandrene as a common component. The findings highlight the environmental impact of green products and their effectiveness (Harding-Smith et al., 2024).
- RNA-Seq-Based Transcriptomics and GC-MS Quantitative Analysis Reveal Antifungal Mechanisms of Essential Oil of Clausena lansium (Lour.) Skeels Seeds against Candida albicans.: The study uses RNA-Seq and GC-MS to investigate the antifungal properties of Clausena lansium essential oil, which contains a-phellandrene, against Candida albicans, providing insights into its potential therapeutic applications (Ma et al., 2023).
- Unveiling the Anti-Cholera and Active Diabetic Renoprotective Compounds of Maqian Essential Oil: A Computational and Molecular Dynamics Study.: This study identifies a-phellandrene as an active compound in Maqian essential oil with anti-cholera and renoprotective effects, suggesting its potential for treating cholera and protecting against diabetic renal damage (Dahab et al., 2023).
- Electrophysiological and Behavioral Responses of Batocera horsfieldi Hope to Volatiles from Pistacia chinensis Bunge.: This research examines the responses of Batocera horsfieldi to volatiles, including a-phellandrene, from Pistacia chinensis. The findings have implications for pest management strategies using natural volatiles (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
WGK
WGK 2
闪点(°F)
116.6 °F
闪点(°C)
47 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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
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
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
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
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
实验方案
-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene
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