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C109401

Sigma-Aldrich

Cyclooctane

≥99%

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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

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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

C109401-2.5L:
C109401-VAR:
C109401-BULK:
C109401-100ML:
C109401-500ML:
C109401-5ML:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBK3666
SHBK1739
SHBK1738
SHBK1737
SHBK1736

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Sigma-Aldrich

C110507

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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)
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
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
Péter Kele et al.
Organic & biomolecular chemistry, 7(17), 3486-3490 (2009-08-14)
The synthesis of a set of new clickable fluorophores that virtually cover the whole visible spectrum reaching the near infra-red regime is presented herein. Besides dyes that are capable of participating in classical copper catalyzed 1,3-dipolar cycloaddition reactions with the
Leo A Paquette et al.
The Journal of organic chemistry, 70(2), 505-509 (2005-01-18)
A program directed to the possible adaptation of ring closing metathesis to a total synthesis of vinigrol is described. With a convenient route to intermediates of general type 3 available from a prior investigation, several candidate substrates were prepared. These
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