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Merck
CN

U407

Undecane

≥99%

Synonym(s):

n-Undecane, Hendecane

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About This Item

Linear Formula:
CH3(CH2)9CH3
CAS Number:
Molecular Weight:
156.31
Beilstein:
1697099
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor density

5.4 (vs air)

Quality Level

vapor pressure

<0.4 mmHg ( 20 °C)

Assay

≥99%

refractive index

n20/D 1.417 (lit.)

bp

196 °C (lit.)

mp

−26 °C (lit.)

density

0.74 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCC

InChI

1S/C11H24/c1-3-5-7-9-11-10-8-6-4-2/h3-11H2,1-2H3

InChI key

RSJKGSCJYJTIGS-UHFFFAOYSA-N

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Application

Undecane is mainly used as a model n-alkane in studies relating to viscosities, excess molar enthalpies and vapor-liquid equilibrium of binary alkane mixtures.

Pictograms

FlameHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Excess enthalpies of decan-1-ol+ n-pentane,+ n-hexane,+ n-heptane,+ n-octane,+ n-nonane,+ n-decane, and+ n-undecane at 298.15 K.
Kumaran M K and Benson G C
The Journal of Chemical Thermodynamics, 16(2), 175-182 (1984)
Measurements of the viscosity of n-heptane, n-nonane, and n-undecane at pressures up to 70 MPa.
Assael M J and Papadaki M
International Journal of Thermophysics, 12(5), 801-810 (1991)
A general correlation of vapor?liquid equilibria in hydrocarbon mixtures.
Chao K C and Seader J D
AIChE Journal, 7(4), 598-605 (1961)
C Yohannan Panicker et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(5), 1559-1565 (2010-03-17)
Fourier-transform-Raman and infrared spectrum of 4-azatricyclo [5.2.2.0(2,6)] undecane-3,5,8-trione were recorded and analyzed. The vibrational wavenumbers were examined theoretically using the Gaussian03 set of quantum chemistry codes, and the normal modes were assigned by potential energy distribution (PED) calculations. The first
Kye-Simeon Masters et al.
The Journal of organic chemistry, 73(20), 8081-8084 (2008-09-19)
In a study directed at developing a concise approach to the polycyclic core of frondosin D, a Stille-Heck sequence has been identified that gives direct access to the trimethylbicyclo[5.4.0]undecane ring system common to all frondosins.

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