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150584

Sigma-Aldrich

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
Beilstein:
1735221
EC Number:
203-956-9
MDL number:
MFCD00004747
UNSPSC Code:
12352100
PubChem Substance ID:
24849047
NACRES:
NA.22

vapor density

4.5 (vs air)

Quality Level

100

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.)

SMILES string

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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Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
Shuo-Yang Wei et al.
Journal of chromatography. A, 1218(51), 9142-9148 (2011-11-22)
A novel method using sample preparation method, "ultrasound-assisted emulsification microextraction" (USAEME) with manual shaking, coupled with gas chromatography using and an electron capture detector (GC-ECD) was developed for the analysis of organochlorine pesticides (OCPs) in aqueous samples. The apparatus is
Christopher S Lunde et al.
Antimicrobial agents and chemotherapy, 53(8), 3375-3383 (2009-05-28)
Telavancin is an investigational lipoglycopeptide antibiotic currently being developed for the treatment of serious infections caused by gram-positive bacteria. The bactericidal action of telavancin results from a mechanism that combines the inhibition of cell wall synthesis and the disruption of
Grit Neumann et al.
Applied and environmental microbiology, 72(6), 4232-4238 (2006-06-06)
The solvent-tolerant strain Pseudomonas putida DOT-T1E was grown in batch fermentations in a 5-liter bioreactor in the presence and absence of 10% (vol/vol) of the organic solvent 1-decanol. The growth behavior and cellular energetics, such as the cellular ATP content
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
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