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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

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

29598-1ML:
29598-VAR:
29598-BULK:
29598-5ML:

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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
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
Josep M Porta et al.
Journal of computational chemistry, 34(3), 234-244 (2012-09-28)
The conformational space of a flexible molecular loop includes the set of conformations fulfilling the geometric loop-closure constraints and its energy landscape can be seen as a scalar field defined on this implicit set. Higher-dimensional continuation tools, recently developed in
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
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.
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