Skip to Content
Merck
CN

155330

Cyclodecane

≥90%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C10H20
CAS Number:
Molecular Weight:
140.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-032-3
Beilstein/REAXYS Number:
1900637
MDL number:
Assay:
≥90%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

LMGZGXSXHCMSAA-UHFFFAOYSA-N

InChI

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

SMILES string

C1CCCCCCCCC1

assay

≥90%

form

liquid

Quality Level

bp

201 °C (lit.)

mp

9-10 °C (lit.)

density

0.871 g/mL at 25 °C (lit.)

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

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)


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service