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Merck
CN

442539

1-癸醇

analytical standard

别名:

C10 醇, 正癸醇

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关于此项目

线性分子式:
CH3(CH2)9OH
化学文摘社编号:
分子量:
158.28
Beilstein:
1735221
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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等级

analytical standard

质量水平

蒸汽密度

4.5 (vs air)

蒸汽压

1 mmHg ( 70 °C)
8.25 mmHg ( 100 °C)

CofA

current certificate can be downloaded

自燃温度

550 °F

包装

ampule of 1000 mg

技术

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.437 (lit.)

沸点

231 °C (lit.)

mp

5-7 °C (lit.)

溶解性

H2O: slightly soluble 0.0211 g/L at 20 °C

密度

0.829 g/mL at 25 °C (lit.)

应用

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

包装形式

neat

储存温度

2-30°C

SMILES字符串

CCCCCCCCCCO

InChI

1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3

InChI key

MWKFXSUHUHTGQN-UHFFFAOYSA-N

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一般描述

1-Decanol can be obtained via decomposition of decyl hydroperoxide or dehydrogenation of 1-decene, followed by hydrolysis.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

应用

1-Decanol can find applications as a solvent in order to recover morpholine, via extraction of morpholine from the aqueous effluent in rubber, petrochemical, dye, coking plants, resin and also organo-chemical industries.
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

Aquatic Chronic 3 - Eye Irrit. 2

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

203.0 °F - Pensky-Martens closed cup

闪点(°C)

95 °C - Pensky-Martens 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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Isobaric phase equilibrium of morpholine+ 1-decanol, volumetric properties and molar refractivity from 293.15 to 333.15 K of morpholine+ 1-decanol and 1-octanol+ toluene system with applications of Prigogine?Flory?Patterson theory
Kumari A, et al.
Thermochimica Acta, 649, 41-53 (2017)
Groundwater Chemicals Desk Reference (2010)
Maria Paola Tampieri et al.
Mycopathologia, 159(3), 339-345 (2005-05-11)
Many volatile oils are known to possess antifungal properties and are potentially applicable as antimycotic agents. By studying the efficacy of essential oils against different pathogenic mycetes, we have evaluated the in-vitro inhibiting activity of some essential oils and their
Maen M Husein et al.
Journal of colloid and interface science, 288(2), 457-467 (2005-06-02)
A novel method of preparing AgCl nanoparticles by mixing AgCl powder and a microemulsion consisting of dioctyldimethylammonium chloride/n-decanol/water/isooctane is introduced. This new method was discovered during the preparation of AgCl nanoparticles in single microemulsions by direct reaction with the dioctyldimethylammonium
Agnieszka Szarecka et al.
Biophysical journal, 93(6), 1895-1905 (2007-05-22)
The new crystal structures of the product-bound firefly luciferase combined with the previously determined substrate-free structures allow for a detailed analysis of the dynamics basis for the luciferase enzymatic activities. Using the Gaussian network model and the anisotropic network model

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