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Sigma-Aldrich

Cyclodecane

≥90%

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About This Item

Empirical Formula (Hill Notation):
C10H20
CAS Number:
293-96-9
Molecular Weight:
140.27
Beilstein/REAXYS Number:
1900637
EC Number:
206-032-3
MDL number:
MFCD00003711
UNSPSC Code:
12352100
PubChem Substance ID:
24849518
NACRES:
NA.22

assay

≥90%

form

liquid

refractive index

n20/D 1.471 (lit.)

bp

201 °C (lit.)

mp

9-10 °C (lit.)

density

0.871 g/mL at 25 °C (lit.)

SMILES string

C1CCCCCCCCC1

InChI

1S/C10H20/c1-2-4-6-8-10-9-7-5-3-1/h1-10H2

InChI key

LMGZGXSXHCMSAA-UHFFFAOYSA-N

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General description

The concentration-dependent diffusion rate of cyclodecane has been studied.

Application

Cyclodecane was used in the hydrolysis of GM1.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Yu Wang et al.
Langmuir : the ACS journal of surfaces and colloids, 29(9), 2935-2945 (2013-01-31)
The structure of a molecule and its concentration can strongly influence diffusional properties for transport in nanoporous materials. We study mass transfer of alkanes in BPL activated carbon using the concentration-swing frequency response method, which can easily discriminate among mass
T Kurita et al.
Journal of lipid research, 41(5), 846-851 (2000-04-29)
Lysoglycosphingolipids were produced from glycosphingolipids by using sphingolipid ceramide N-deacylase, which cleaves the N-acyl linkage between fatty acids and sphingosine bases in various glycosphingolipids. The enzyme reaction was done in a biphasic media prepared with water;-immiscible organic solvent and aqueous

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