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30570

Sigma-Aldrich

Decane

≥95%

Synonym(s):

n-Decane

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About This Item

Linear Formula:
CH3(CH2)8CH3
CAS Number:
Molecular Weight:
142.28
Beilstein/REAXYS Number:
1696981
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.9 (vs air)

vapor pressure

1 mmHg ( 16.5 °C)
3.77 mmHg ( 37.7 °C)

assay

≥95%

form

liquid

autoignition temp.

410 °F

expl. lim.

2.6 %

refractive index

n20/D 1.411 (lit.)
n20/D 1.412

bp

170.0-182.0 °C
174 °C (lit.)

mp

−30 °C (lit.)

density

0.730 g/mL at 20 °C
0.73 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCC

InChI

1S/C10H22/c1-3-5-7-9-10-8-6-4-2/h3-10H2,1-2H3

InChI key

DIOQZVSQGTUSAI-UHFFFAOYSA-N

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General description

Decane is an organic solvent. Bifunctional conversion of decane over Pt/ZSM-22, Pt/ZSM-5 and Pt/USY catalysts was compared. Structure of single-phase (sodium di-2-ethylsulfosuccinate)/D2O/decane microemulsions was investigated by small-angle neutron scattering.

Application

Decane was used as solvent to investigate the self-association of cyclohexanols.

pictograms

FlameHealth hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

114.8 °F - closed cup

flash_point_c

46.0 °C - closed cup

ppe

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


Certificates of Analysis (COA)

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Self-association of cyclohexanols in inert solvents. Apparent heat capacities of cyclohexanol and substituted cyclohexanols in n-heptane and n-decane.
Trejo LM, et al.
J. Chem. Soc., Faraday, 87(11), 1739-1743 (1991)
Structure of Dense Sodium Di-2-Ethylsulfosuccinate/D 2 O/Decane Microemulsions.
Kotlarchyk M, et al.
Physical Review Letters, 53(9), 941-941 (1984)
Selective conversion of decane into branched isomers: A comparison of platinum/ZSM-22, platinum/ZSM-5 and platinum/USY zeolite catalysts.
Martens JA, et al.
Applied Catalysis, 76(1), 95-116 (1991)
Mahvash Karimi et al.
Colloids and surfaces. B, Biointerfaces, 95, 129-136 (2012-03-27)
Wettability alteration is considered to be one of the important mechanisms that lead to increased oil recovery during microbial enhanced oil recovery (MEOR) processes. Changes in wettability will greatly influence the petrophysical properties of the reservoir rocks and determine the
Ching-Wei Njauw et al.
Langmuir : the ACS journal of surfaces and colloids, 29(12), 3879-3888 (2013-02-28)
It has been known that the addition of bile salts to lecithin organosols induces the formation of reverse wormlike micelles and that the worms are similar to long polymer chains that entangle each other to form viscoelastic solutions. In this

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