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1,8-BIS-MALEIMIDOTRIETHYLENEGLYCOL

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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

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

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