Name: | 1,8-BIS-MALEIMIDOTRIETHYLENEGLYCOL |
CAS: | 115597-84-7 |
Synonyms: | 1,8-BIS-MALEIMIDOTETRAETHYLENEGLYCOL ; 1,8-BIS-MALEIMIDO-(PEO)3 ; 1,8-BIS(MALEIMIDO)-3,6-DIOXAOCTANE ; BM(PEO)3 ; ABLOCK AB-13-6093 ; 1,8-BIS-MALEIMIDOTRIETHYLENEGLYCOL ; 2,2'-(ETHYLENEDIOXY)BIS(ETHYLMALEIMIDE) |
MDL.: | MFCD01096749 |
H bond acceptor: | 8 |
H bond donor: | 0 |
Smile: | C1=CC(=O)N(C1=O)CCOCCOCCN2C(=O)C=CC2=O |
InChi: | InChI=1S/C14H16N2O6/c17-11-1-2-12(18)15(11)5-7-21-9-10-22-8-6-16-13(19)3-4-14(16)20/h1-4H,5-10H2 |
InChiKey: | InChIKey=FERLGYOHRKHQJP-UHFFFAOYSA-N |
Property |
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Comments: | EIGHT-ATOM POLYETHER SPACER REDUCES POTENTIAL FOR CONJUGATE PRECIPITATION IN SULFHYDRYL-TO-SULFHYDRYL CROSS-LINKING APPLICATIONS FEATURES/BENEFITS: IDEAL FOR SMALL MOLECULE OR PEPTIDE CONJUGATIONS FEATURES/BENEFITS: LONG SULFHYDRYL-REACTIVE, HOMOBIFUNCTIONAL CROSS-LINKER FEATURES/BENEFITS: MALEIMIDES REACT WITH -SH GROUPS AT PH 6.5-7.5, FORMING STABLE THIOETHER LINKAGES FEATURES/BENEFITS: NON-CLEAVABLE; WATER-SOLUBLE FEATURES/BENEFITS: POLYETHYLENE OXIDE (PEO) CROSS-BRIDGE PROVIDES INCREASED WATER SOLUBILITY, REDUCING THE POTENTIAL FOR CROSS-LINKER-CAUSED PRECIPITATION OF CONJUGATES FEATURES/BENEFITS: REACTIVE GROUPS: MALEIMIDE (HOMOBIFUNCTIONAL) FEATURES/BENEFITS: REACTIVE TOWARD: SULFHYDRYL GROUPS |
Information: | SPACER ARM 14.7 ANGSTROM |
Safety information |
1,8-BIS-MALEIMIDOTRIETHYLENEGLYCOL
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