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Merck
CN

11107

Supelco

α-细辛脑

analytical standard

别名:

反式-1,2,4-三甲氧基-5-(1-丙烯基)苯, 反式-1-丙烯基-2,4,5-三甲氧基苯

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关于此项目

线性分子式:
(CH3O)3C6H2CH=CHCH3
化学文摘社编号:
分子量:
208.25
Beilstein:
1910606
EC 号:
MDL编号:
UNSPSC代码:
85151701
PubChem化学物质编号:
NACRES:
NA.24
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等级

analytical standard

质量水平

方案

≥97.0% (GC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

296 °C (lit.)

mp

57-61 °C (lit.)
57-61 °C

应用

food and beverages

包装形式

neat

SMILES字符串

COc1cc(OC)c(\C=C\C)cc1OC

InChI

1S/C12H16O3/c1-5-6-9-7-11(14-3)12(15-4)8-10(9)13-2/h5-8H,1-4H3/b6-5+

InChI key

RKFAZBXYICVSKP-AATRIKPKSA-N

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一般描述

Asarones are toxic morphogenetic agents. It is also known for its chemosterlant and oviposition stimulant properties. Naturally it can be extracted from Acorus calamus. α-Asarone is considered as growth inhibitor. This isomer acts as antifeedant with less toxicity.

应用

It was used as standard in synthesis of five isomers of α-Asarone to compare the better deterrent using HPLC analysis.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Feeding-deterrent activity of a-asarone isomers against some stored Coleoptera.
Poplawski, Janusz, et al.
Pest Management Science, 56.6, 560-564 (2000)
Daijie Wang et al.
Journal of separation science, 34(23), 3339-3343 (2011-11-01)
In this study, supercritical fluid extraction (SFE) was used to extract essential oil from Acorus tatarinowii Schott under the pressure of 25 MPa and temperature of 35°C. Two (E)- and (Z)-diastereomers of α-asarone and β-asarone were separated and purified by
Jadwiga Marczewska et al.
Acta poloniae pharmaceutica, 70(2), 349-354 (2013-04-26)
In our previous paper we examined mutagenic and genotoxic activity of 4 alpha-asarone isomers 2-5 exhibiting relatively high hypolipidemic activity. In the present paper, we examined genotoxic activity of alpha-asarone and its isomers as the ability to damage cellular DNA
De-Jia Zou et al.
Die Pharmazie, 66(1), 44-51 (2011-03-12)
Beta-amyloid (Abeta) toxicity has been postulated to initiate synaptic loss and subsequent neuronal degeneration seen in Alzheimer's disease (AD). We previously demonstrated that beta-asarone improves cognitive function by suppressing neuronal apoptosis in vivo. In this study, we assessed the neuroprotective
Yong Qi Fang et al.
European journal of drug metabolism and pharmacokinetics, 37(3), 187-190 (2012-02-22)
The objective of this work was to analyze transformation and excretion of β-asarone in rabbits with gas chromatography-mass spectrometry (GC-MS). The rabbits were administered IV at a dose of 30 mg/kg body weight β-asarone-water-propylene glycol (6:34:60, v/v/v), and urine and

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