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29598

Supelco

Cyclooctane

analytical standard

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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:
41116107
PubChem Substance ID:
329753379
NACRES:
NA.24

grade

analytical standard

vapor pressure

16 mmHg ( 37.7 °C)

Assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.458 (lit.)
n20/D 1.458

bp

151 °C/740 mmHg (lit.)

mp

10-13 °C (lit.)

density

0.834 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

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

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW3338
BCBQ2442V
BCBL3173V
BCBF9061V
1433366V

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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
Heidi E Bostic et al.
Chemical communications (Cambridge, England), 48(10), 1431-1433 (2011-10-04)
Copper-free click chemistry was employed to derivatize membrane bilayers. This approach uses an azido-lipid conjugate presented on liposomes, which can be labeled in bioorthogonal fashion via cyclooctyne-tagged reagents. An immobilization-based approach using streptavidin-coated microplates was exploited to evaluate membrane derivatization.
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
Leo A Paquette et al.
The Journal of organic chemistry, 71(12), 4353-4363 (2006-06-06)
D-Arabinose and D-glucose are transformed into the identical vinyl furanoside, whose role is to serve as the precursor to enantiopure cyclooctadienone 6. The key steps of this relay involve a zirconocene-promoted ring contraction and [3,3] sigmatropic rearrangement of an enynol.
W Michael Brown et al.
The Journal of chemical physics, 129(6), 064118-064118 (2008-08-22)
Dimensionality reduction approaches have been used to exploit the redundancy in a Cartesian coordinate representation of molecular motion by producing low-dimensional representations of molecular motion. This has been used to help visualize complex energy landscapes, to extend the time scales
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