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297879

Sigma-Aldrich

Dodecane

anhydrous, ≥99%

Synonym(s):

n-Dodecane

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About This Item

Linear Formula:
CH3(CH2)10CH3
CAS Number:
Molecular Weight:
170.33
Beilstein/REAXYS Number:
1697175
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.21

grade

anhydrous

Quality Level

vapor density

5.96 (vs air)

vapor pressure

1 mmHg ( 47.8 °C)

assay

≥99%

form

liquid

autoignition temp.

401 °F

expl. lim.

8 %

impurities

<0.003% water
<0.005% water (100 mL pkg)

refractive index

n20/D 1.421 (lit.)

bp

215-217 °C (lit.)

mp

−9.6 °C (lit.)

density

0.75 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCC

InChI

1S/C12H26/c1-3-5-7-9-11-12-10-8-6-4-2/h3-12H2,1-2H3

InChI key

SNRUBQQJIBEYMU-UHFFFAOYSA-N

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General description

Dodecane is a linear alkane mainly found in jet fuels.

Application

Dodecane may be used as an inorganic diluent to form an organic phase along with decanol as an active diluent and tri-n-octylamine as an extractant. This system may be used for the extraction of lactic acid from aqueous solutions.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1

supp_hazards

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

158.0 °F - Pensky-Martens closed cup

flash_point_c

70 °C - Pensky-Martens closed cup

ppe

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


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1 of 2

Thermal decomposition of n-dodecane: Experiments and kinetic modeling.
Herbinet O, et al.
Journal of Analytical and Applied Pyrolysis, 78(2), 419-429 (2007)
Lactic acid extraction from aqueous solutions with tri-n-octylamine dissolved in decanol and dodecane
Yankov D, et al.
Biochemical Engineering Journal, 21(1), 63-71 (2004)
The novel extractants, diglycolamides, for the extraction of lanthanides and actinides in HNO3-n-dodecane system.
Sasaki Y, et al.
Solvent Extr. Ion Exch., 19(1), 91-103 (2001)
E J Walsh et al.
Biomedical microdevices, 8(1), 59-64 (2006-02-24)
The two-phase segmented flow approach to the processing and quantitative analysis of biological samples in microdevices offers significant advantages over the single-phase continuous flow methodology. Despite this, little is known about the compatibility of samples and reactants with segmenting fluids
Hydroisomerization and hydrocracking. 2. Product distributions from n-decane and n-dodecane.
Steijns M, et al.
Ind. Eng. Chem. Prod. Res. Dev., 20(4), 654-660 (1981)

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