跳转至内容
Merck
CN
所有图片(1)

主要文件

查看所有文档

W263508

Sigma-Aldrich

芳樟醇

≥97%, FCC, FG

别名:

(±)-3,7-二甲基-3-羟基-1,6-辛二烯, (±)-二甲基-1,6-辛二烯-3-醇

登录查看公司和协议定价
所有图片(1)

About This Item

线性分子式:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS号:
78-70-6
分子量:
154.25
FEMA编号:
2635
Beilstein:
1721488
EC 号:
201-134-4
欧洲委员会编号:
61
MDL编号:
MFCD00008906
UNSPSC代码:
12164502
PubChem化学物质编号:
24901212
Flavis编号:
2.013
NACRES:
NA.21
性状检查:
lemon; orange; floral; sweet
等级:
FG
Fragrance grade
Halal
Kosher
生物来源:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
食品过敏原:
no known allergens

生物来源

synthetic

质量水平

400

等级

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 182.60

蒸汽压

0.17 mmHg ( 25 °C)

方案

≥97%

组成

contains EU 1223/2009 restricted linalool

折射率

n20/D 1.462 (lit.)

沸点

194-197 °C/720 mmHg (lit.)

溶解性

ethanol: soluble 1ml/4ml, clear, colorless (60% ethanol)

密度

0.87 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

致敏芳香化合物

linalool

性状检查

lemon; orange; floral; sweet

SMILES字符串

C\C(C)=C\CCC(C)(O)C=C

InChI

1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3

InChI key

CDOSHBSSFJOMGT-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

芳樟醇或((±)-3,7-二甲基-1,6-辛二烯-3-醇是一种香料。
芳樟醇是一种单萜化合物，是很多精油中的主要成分。已有研究报告天然对映体(−)芳樟醇的抗炎性。它也是罗勒和百里香精油中的主要成分。芳樟醇散发柠檬香气。

应用

芳樟醇已被用于研究各种花芳香化合物的混合物，作为迁徙性飞蛾绒毛虫 ( Anticarsia gemmatalis Hübner) 的花引诱剂。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H317,H319

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

171.0 °F - Pensky-Martens closed cup

闪点(°C)

77.2 °C - Pensky-Martens closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBQ9059
SHBQ1776
SHBP8125
SHBP0723
SHBN4536

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Inhibitory effect of thyme and basil essential oils, carvacrol, thymol, estragol, linalool and p-cymene towards Shigella sonnei and S. flexneri.
Bagamboula CF, et al.
Food Microbiology, 21(1), 33-42 (2004)
H M Schellinck et al.
Chemical senses, 26(6), 663-672 (2001-07-28)
The present paper describes a quick and efficient method for assessing olfactory discrimination learning in mice. In training mice received trials in which one odor (CS+) was paired with sugar and another odor (CS-) was paired with no sugar. When
Transformations of monoterpenoids in aqueous acids: The reactions of linalool. geraniol, nerol and their acetates in aqueous citric acid.
Baxter RL ,et al.
Tetrahedron, 34(14), 2195-2199 (1978)
Binary floral lure attractive to velvetbean caterpillar adults (Lepidoptera: Noctuidae).
Meagher RL and Landolt PJ.
Florida entomologist, 93(1), 73-79 (2010)
L Re et al.
Pharmacological research, 42(2), 177-182 (2000-07-11)
Linalool is a monoterpene compound reported to be a major component of essential oils in various aromatic species. Several linalool-producing species are used in traditional medical systems. Among these is Aeolanthus suaveolens G. Dom (Labiatae) which is used as an
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门