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Merck

163333

Sigma-Aldrich

香叶醇

98%

别名:

反式-3,7-二甲基-2,6-辛二烯-1-醇

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About This Item

线性分子式:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2OH
CAS号:
分子量:
154.25
Beilstein:
1722456
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

5.31 (vs air)

蒸汽壓力

~0.2 mmHg ( 20 °C)

化驗

98%

形狀

liquid

折射率

n20/D 1.474 (lit.)

bp

229-230 °C (lit.)

溶解度

water: soluble 0.1 g/L at 25 °C

密度

0.879 g/mL at 20 °C (lit.)

SMILES 字串

C\C(C)=C\CC\C(C)=C\CO

InChI

1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+

InChI 密鑰

GLZPCOQZEFWAFX-JXMROGBWSA-N

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一般說明

香叶醇在含有介孔分子筛的含铬催化的超临界二氧化碳中经过分子氧氧化,得到柠檬醛

應用

香叶醇用于合成草食动物诱导的植物挥发物的现场评估,作为有益昆虫的引诱剂。它被用于评估体外体内类异戊二烯的肿瘤抑制能力

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

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

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

226.4 °F - closed cup

閃點(°C)

108 °C - closed cup

個人防護裝備

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


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Selective catalytic oxidation of geraniol to citral with molecular oxygen in supercritical carbon dioxide.
Dapurkar SE, et al.
Applied Catalysis A: General, 394(1), 209-214 (2011)
Maria Cristina Bonferoni et al.
Pharmaceutics, 11(3) (2019-03-06)
The pharmacological activities of geraniol include anticancer and neuroprotective properties. However, its insolubility in water easily induces separation from aqueous formulations, causing administration difficulties. Here we propose new emulsified formulations of geraniol by using the amphiphilic polymer chitosan-oleate (CS-OA) as
L He et al.
The Journal of nutrition, 127(5), 668-674 (1997-05-01)
Sundry mevalonate-derived constituents (isoprenoids) of fruits, vegetables and cereal grains suppress the growth of tumors. This study estimated the concentrations of structurally diverse isoprenoids required to inhibit the increase in a population of murine B16(F10) melanoma cells during a 48-h
Ying Zhou et al.
Biomolecules, 9(12) (2019-12-06)
When insects attack plants, insect-derived elicitors and mechanical damage induce the formation and emission of plant volatiles that have important ecological functions and flavor properties. These events have mainly been studied in model plants, rather than crop plants. Our study
Layane da Silva Corrêa et al.
Applied biochemistry and biotechnology, 190(2), 574-583 (2019-08-10)
This article describes the synthesis of terpenic esters derived from geraniol and citronellol (geranyl and citronellyl alkanoates) through esterification reactions catalyzed by the immobilized lipases from Thermomyces lanuginosus (Lipozyme TL IM®) and Candida antarctica (Novozym 435®). Geraniol was esterified with

实验方案

-(+)-Limonene, purum, ≥98.0% (sum of enantiomers, GC); Geranyl tiglate; α-Terpineol, natural, ≥96%, FCC, FG; Geranyl formate; α-Pinene

-3,7-Dimethyl-2,6-octadien-1-ol; Neral; Geraniol; Geranial; Undecanal; Citronellyl acetate; Neryl acetate; 3,7-Dimethyl-2,6-octadienyl acetate; 1-Tetradecene; Tetradecane; α-Bisabolol

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