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:
Molecular Weight:
158.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-956-9
Beilstein/REAXYS Number:
1735221
MDL number:
Assay:
98%
Form:
liquid
vapor density
4.5 (vs air)
Quality Level
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
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
Application
1-Decanol was used to study the thermal properties of polymer-monolithic stationary phases.
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signalword
Warning
hcodes
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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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
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