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Merck
CN

745057

(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl N-{2-[(2-aminoethyl)disulfanyl]ethyl}carbamate

Synonym(s):

BCN-S-S-amine

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About This Item

Empirical Formula (Hill Notation):
C15H24N2O2S2
CAS Number:
Molecular Weight:
328.49
PubChem Substance ID:
UNSPSC Code:
12352200
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InChI

1S/C15H24N2O2S2/c16-7-9-20-21-10-8-17-15(18)19-11-14-12-5-3-1-2-4-6-13(12)14/h12-14H,3-11,16H2,(H,17,18)/t12-,13+,14-

InChI key

COXJSXQCKNEICM-BTTYYORXSA-N

SMILES string

NCCSSCCNC(=O)OCC1[C@@H]2CCC#CCC[C@H]12

storage temp.

−20°C

General description

Amine functionalized cyclooctyne derivative for incorporation of the cyclooctyne moiety into carboxylic acid containing compounds or biomolecules. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne click chemistry reactions. This strained cyclooctyne will react with azide functionalized compounds or biomolecules without the need for a copper catalyst to result in a stable triazole linkage. The disulfide present can be readily cleaved using mild reducing conditions (10-50 mM DTT at 37°C for 30 min or 5% β-mercaptoethanol in SDS-PAGE sample buffer at 100°C for 5 minutes).

Disclaimer

Please avoid reducing agents and amine or azide containing buffers during coupling/labeling reactions. Only use reducing agents when cleavage of the disulfide is desired.

pictograms

Exclamation mark

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Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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