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Merck

W333301

Sigma-Aldrich

3-正丁烯基苯酞

mixture of cis and trans isomers, ≥96%, FG

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About This Item

经验公式(希尔记法):
C12H12O2
CAS号:
分子量:
188.22
FEMA编号:
3333
EC 号:
欧洲委员会编号:
10083
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
10.024
NACRES:
NA.21

生物来源

synthetic

等级

FG
Halal
Kosher

管理合规性

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

方案

≥96%

折射率

n20/D 1.577 (lit.)

沸点

139-142 °C/5 mmHg (lit.)

密度

1.103 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

herbaceous

SMILES字符串

CCC\C=C1/OC(=O)c2ccccc12

InChI

1S/C12H12O2/c1-2-3-8-11-9-6-4-5-7-10(9)12(13)14-11/h4-8H,2-3H2,1H3/b11-8-

InChI key

WMBOCUXXNSOQHM-FLIBITNWSA-N

一般描述

3-丁烯基苯酞是川芎的生物活性苯酞化合物,川芎来源于川芎(Ligusticum chuanxiong Hort)根部,是一种用于治疗头痛的中草药。

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 2

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Pharmacodynamic action and mechanism of volatile oil from Rhizoma Ligustici Chuanxiong Hort. on treating headache.
Peng C, et al.
Phytomedicine, 16(1), 25-34 (2004)
Sunny Sun-Kin Chan et al.
Journal of ethnopharmacology, 122(2), 308-312 (2009-02-03)
Ligusticum chuanxiong Hort. (Umbelliferae), a traditional Chinese medicinal herb, is often prescribed together with nitric oxide donors for treating coronary heart diseases such as angina in China; however, studies concerning their pharmacological interaction are scarce. The objective of the present
Yung-Luen Yu et al.
Journal of agricultural and food chemistry, 58(3), 1630-1638 (2010-01-02)
Epigenetic alteration of DNA methylation plays an important role in the regulation of gene expression associated with chemosensitivity of human hepatocellular (HCC) carcinoma cells. With the aim of improving the chemotherapeutic efficacy for HCC, the effect of the naturally occurring
Ju-Ching Yeh et al.
Journal of chromatography. A, 1236, 132-138 (2012-03-31)
In natural product research, it is a common experience that fractionation of biologically-active crude extracts can lead to the loss of their original activity. This is attributed to synergistic effects, where two or more components are required to be present
Li-Fu Chang et al.
Journal of surgical oncology, 103(5), 442-450 (2011-01-20)
In previous study, n-butylidenephthalide (BP), a natural compound from Angelica sinensis, has anti-glioblastoma multiform (GBM) cell effects. In this study, we modified BP structure to increase anti-GBM cell effects. The anti-GBM cell effects of one derivative of BP, (Z)-N-(2-(dimethylamino)ethyl)-2-(3-((3-oxoisobenzofuran-1(3H)-ylidene)methyl)phenoxy)acetamide (PCH4)

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