768804
BCN-POE3-NH-lissamine™ rhodamine B conjugate
别名:
5-(N-{1-[(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-yl]-3-oxo- 2,7,10-trioxa-4-azadodecan-12-yl]sulfamoyl}-2-[6- (diethylamino)-3-(diethyliminio)-3H-xanthen-9- yl]benzenesulfonate, BCN-lissamine™ rhodamine B conjugate
登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
storage temp.
−20°C
SMILES string
[H][C@@]12CCC#CCC[C@]1([H])[C@@H]2COC(NCCOCCOCCNS(=O)(C3=CC=C(C(C(C=CC(N(CC)CC)=C4)=C4O5)=C6C5=CC(C=C6)=[N+](CC)CC)C(S([O-])(=O)=O)=C3)=O)=O
InChI
1S/C44H56N4O10S2/c1-5-47(6-2)31-15-18-36-40(27-31)58-41-28-32(48(7-3)8-4)16-19-37(41)43(36)38-20-17-33(29-42(38)60(52,53)54)59(50,51)46-22-24-56-26-25-55-23-21-45-44(49)57-30-39-34-13-11-9-10-12-14-35(34)39/h15-20,27-29,34-35,39,46H,5-8,11-14,21-26,30H2,1-4H3,(H-,45,49,52,53,54)/t34-,35+,39-
InChI key
ZMENVOKFFFDNLT-JUPLXENESA-N
General description
This BCN-lissamine rhodamine B conjugate is a versatile fluorescent reagent for labeling azide containing compounds or biomolecules. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne click chemistry reactions.This cyclooctyne derivative will react with azide-functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage. Subsequent labeled molecules can be visualized by fluorescence spectroscopy.
Other Notes
Spectral Properties: Abs/Em = 559/578 nm, molar absorbance: 120,000 M-1cm-1
Legal Information
Lissamine is a trademark of PerkinElmer Inc.
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有