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Sigma-Aldrich

Decane

≥95%

Synonym(s):

n-Decane

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About This Item

Linear Formula:
CH3(CH2)8CH3
CAS Number:
124-18-5
Molecular Weight:
142.28
Beilstein:
1696981
EC Number:
204-686-4
MDL number:
MFCD00008954
UNSPSC Code:
12352100
PubChem Substance ID:
57648447
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
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Supplementary Hazards

EUH066

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

114.8 °F - closed cup

Flash Point(C)

46.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Structure of Dense Sodium Di-2-Ethylsulfosuccinate/D 2 O/Decane Microemulsions.
Kotlarchyk M, et al.
Physical Review Letters, 53(9), 941-941 (1984)
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)
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
Kai Sotthewes et al.
Langmuir : the ACS journal of surfaces and colloids, 29(11), 3662-3667 (2013-02-21)
The energetics and dynamics of the various phases of decanethiolate self-assembled monolayers on Au(111) surfaces were studied with scanning tunneling microscopy. We have observed five different phases of the decanethiolate monolayer on Au(111): four ordered phases (β, δ, χ*, and
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