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About This Item
Empirical Formula (Hill Notation):
C8H16
CAS Number:
Molecular Weight:
112.21
Beilstein/REAXYS Number:
1900349
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
16 mmHg ( 37.7 °C)
Quality Level
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.
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk_germany
WGK 2
flash_point_f
82.4 °F - closed cup
flash_point_c
28 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
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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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