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N29406

Sigma-Aldrich

Nonane

ReagentPlus®, 99%

Synonym(s):

n-Nonane

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About This Item

Linear Formula:
CH3(CH2)7CH3
CAS Number:
Molecular Weight:
128.26
Beilstein:
1696917
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.21

Agency

suitable for EPA 1613

vapor density

4.41 (vs air)

vapor pressure

0.18 psi ( 37.7 °C)

product line

ReagentPlus®

Assay

99%

form

liquid

autoignition temp.

401 °F

expl. lim.

2.9 %

refractive index

n20/D 1.405 (lit.)

bp

151 °C (lit.)

mp

−53 °C (lit.)

density

0.718 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCC

InChI

1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3

InChI key

BKIMMITUMNQMOS-UHFFFAOYSA-N

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General description

Nonane is a linear alkane that is mainly obtained from petroleum distillate. It is used as a solvent in organic synthesis.

Application

Nonane (n-Nonane) can be used as a solvent in:      
  • The Ullman reaction and the hydrogenation of CO2 to form CH3OH in the presence of a copper catalyst.      
  • The porosity characterization of different carbons by “nonane blocking of micropores”.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31.0 °C - closed cup


Certificates of Analysis (COA)

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Characterization of single wall carbon nanotubes by nonane preadsorption.
Byl O, et al.
Carbon, 44(10), 2039-2044 (2006)
Measurement of triglycerides using nonane extraction and colorimetry.
A L Levy
Annals of clinical laboratory science, 2(6), 474-479 (1972-11-01)
Oxidation kinetics of n-nonane: Measurements and modeling of ignition delay times and product concentrations.
Rotavera B, et al.
Proceedings of the Combustion Institute, 33(1), 175-183 (2011)
Heat capacities and densities of liquid n-octane, n-nonane, n-decane, and n-hexadecane at temperatures from 318.15 K to 373.15 K and at pressures up to 10 MPa.
Banipal TS, et al.
The Journal of Chemical Thermodynamics, 23(10), 923-931 (1991)
Johanna Faist et al.
European journal of medicinal chemistry, 45(1), 179-185 (2009-11-03)
N-Alkyl and N-(2-dialkylaminoethyl) derivatives of 5-amino-2-azabicyclo-nonanes were prepared and tested in vitro for their activities against the multidrug-resistant K1 strain of Plasmodium falciparum and Trypanosoma brucei rhodesiense (STIB 900). Most of the new compounds showed lower antitrypanosomal activity than their

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