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Merck
CN

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
Biological source:
synthetic
Food allergen:
no known allergens
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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

Quality Level

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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。

pictograms

FlameHealth hazard

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
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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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