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Merck

150584

1-Decanol

98%

Synonym(s):

n-Decyl alcohol, Alcohol C10

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About This Item

Linear Formula:
CH3(CH2)9OH
CAS Number:
112-30-1
Molecular Weight:
158.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849047
EC Number:
203-956-9
Beilstein/REAXYS Number:
1735221
MDL number:
MFCD00004747

Product Name

1-Decanol, 98%

InChI key

MWKFXSUHUHTGQN-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCO

vapor density

4.5 (vs air)

vapor pressure

1 mmHg ( 70 °C)
8.25 mmHg ( 100 °C)

assay

98%

form

liquid

autoignition temp.

550 °F

refractive index

n20/D 1.437 (lit.)

bp

231 °C (lit.)

mp

5-7 °C (lit.)

solubility

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

density

0.829 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

100

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Application

1-Decanol was used to study the thermal properties of polymer-monolithic stationary phases.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

203.0 °F - Pensky-Martens closed cup

flash_point_c

95 °C - Pensky-Martens closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6045
SDBB5248
SDBB2810
SDBB0559
SDBB1044

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Sam Wouters et al.
Journal of separation science, 37(1-2), 179-186 (2013-10-30)
Thermal analysis and SEM were employed to gain insights in the different stages of morphology development and the thermal properties of polymer-monolithic stationary phases. The studied system was a thermally initiated free-radical copolymerization reaction at 70°C of styrene and divinylbenzene
Sanhita S Dixit et al.
Langmuir : the ACS journal of surfaces and colloids, 26(9), 6193-6200 (2010-04-07)
We demonstrate the optical manipulation of nanoliter aqueous droplets containing surfactant or lipid molecules and immersed in an organic liquid using near-infrared light. The resulting emulsion droplets are manipulated using both the thermocapillary effect and convective fluid motion. Droplet-pair interactions
Darren J Caven-Quantrill et al.
Journal of chromatography. A, 1218(7), 875-881 (2011-01-11)
A stir bar sorptive extraction (SBSE) method coupled with gas chromatography-mass spectrometry was optimised for the analysis of volatile components of a model wine, based on a previously optimised method used for analysis of the same components in model grape
H Ahumada et al.
The journal of physical chemistry. A, 109(30), 6644-6651 (2006-07-13)
Most drugs have to cross cell membranes to reach their final target. A better understanding of the distribution, interactions, and dynamics of biologically active molecules in model bilayers is of fundamental importance in understanding drug functioning and design. 2H NMR
Anne M Shearrow et al.
Journal of chromatography. A, 1216(36), 6349-6355 (2009-08-01)
Two ionic liquids (IL), namely, 1-methyl-3-octylimidazolium chloride (MOIC) and trihexyltetradecylphosphonium tetrafluoroborate (TTPT) were used to prepare polar and nonpolar sol-gel coatings for capillary microextraction (CME). Bis[(3-methyldimethoxysilyl)propyl] polypropylene oxide (BMPO), containing sol-gel active terminal methoxysilyl groups and polar propylene oxide repeating
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