Skip to Content
Merck
All Photos(3)

Documents

C109401

Sigma-Aldrich

Cyclooctane

≥99%

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C8H16
CAS Number:
292-64-8
Molecular Weight:
112.21
Beilstein:
1900349
EC Number:
206-031-8
MDL number:
MFCD00004162
UNSPSC Code:
12352100
PubChem Substance ID:
24892341
NACRES:
NA.22

vapor pressure

16 mmHg ( 37.7 °C)

Quality Level

200

Assay

≥99%

form

liquid

refractive index

n20/D 1.458 (lit.)

bp

151 °C/740 mmHg (lit.)

mp

10-13 °C (lit.)

density

0.834 g/mL at 25 °C (lit.)

SMILES string

C1CCCCCCC1

InChI

1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2

InChI key

WJTCGQSWYFHTAC-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Cyclooctane can undergo oxidation with hydrogen peroxide in the presence of triethylpropylammonium-functionalized silica and transition metal mono-substituted polyoxotungstates.
Cyclooctane may undergo oxidation with hydrogen peroxide in the presence of triethylpropylammonium-functionalized silica and transition metal mono-substituted polyoxotungstates.

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

82.4 °F - closed cup

Flash Point(C)

28 °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’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Cyclooctene oxide 99%

Sigma-Aldrich

C110507

Cyclooctene oxide

Butylcyclohexane ≥99%

Sigma-Aldrich

110388

Butylcyclohexane

Silica supported transition metal substituted polyoxotungstates: Novel heterogeneous catalysts in oxidative transformations with hydrogen peroxide.
Estrada AC, et al.
Applied Catalysis A: General, 392(1-2), 28-35 (2011)
Pieter van Delft et al.
Organic letters, 12(23), 5486-5489 (2010-11-06)
The conjugation of a ribonucleic acid 16-mer with the cationic amphiphilic peptide penetratin and an anionic hyaluronan tetrasaccharide by means of Cu-free "click" chemistry is reported. The alkyne-functionalized 16-mer was prepared by automated solid-phase synthesis, using a newly developed strained
Raffaella Rossin et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 54(11), 1989-1995 (2013-10-05)
Current pretargeting systems use noncovalent biologic interactions, which are prone to immunogenicity. We previously developed a novel approach based on the bioorthogonal reaction between a radiolabeled tetrazine and an antibody-conjugated trans-cyclooctene (TCO). However, the tumor-to-blood ratio was low due to
Zhong-Ke Yao et al.
Organic letters, 13(1), 134-137 (2010-11-26)
Discovering new carbon building blocks is very significant to advance transition-metal-catalyzed cycloadditions for the synthesis of various-sized ring compounds. A new seven-carbon building block from buta-1,3-dienylcyclopropanes (BDCPs) has been developed, showing that, under the catalysis of [Rh(CO)(2)Cl](2), BDCPs react with
Shawn Martin et al.
The Journal of chemical physics, 132(23), 234115-234115 (2010-06-25)
Understanding energy landscapes is a major challenge in chemistry and biology. Although a wide variety of methods have been invented and applied to this problem, very little is understood about the actual mathematical structures underlying such landscapes. Perhaps the most
View All Related Papers

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