1,6-Bis(maleimido)hexane

CAS : 4856-87-5

Ref. TR-B475500

Informations sur le produit

• Nom: 1,6-Bis(maleimido)hexane
• Synonymes: 1,1'-(1,6-Hexanediyl)bis-1H-pyrrole-2,5-dione, 1,6-Maleimidohexane, GMBMI, N,N'-Hexamethylenebis[maleimide], N,N'-Hexamethylenedimaleimide, NSC 12818, 1,1'-(Hexane-1,6-diyl)bis-1H-pyrrole-2,5-dione, 1,1′-(1,6-Hexanediyl)bis[1H-pyrrole-2,5-dione], 1,1′-hexane-1,6-diylbis(1H-pyrrole-2,5-dione), 1,6-Bismaleimidehexane, 1,6-Bismaleimidohexane, 1,6-Bmh, 1,6-Dimaleimidohexane, 1,6-Hexamethylenebis[maleimide], 1,6-Hexanediylbismaleimide, 1-[6-(2,5-Dioxopyrrol-1-yl)hexyl]pyrrole-2,5-dione, 1H-Pyrrole-2,5-dione, 1,1'-(1,6-hexanediyl)bis-, 1H-Pyrrole-2,5-dione, 1,1'-(1,6-hexanediyl)bis- (9CI), Ai3-51359, BMH Crosslinker, Brn 0253749, Gmbmi, Gp 207R, Hexamethylenediamine bismaleimide, Maleimide, N,N'-hexamethylenedi-, N,N'-Hexamethylenebis(maleimide), Nsc 12818

Description

Applications A sulfhydryl reactive homobifunctional crosslinking reagent. Under mild conditions, will permit irreversible cross-linking of sulfhydral containing compounds at a pH range of 6.5 to 7.5.Spacer Arm: 16.1 Angstroms
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Partis, M.D., et al.: J. Prot. Chem., 2, 263 (1983), Garant, M., et al.: Biochem., 39, 7178 (2000), Costantini, P., et al.: Oncogene, 19, 307 (2000),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 276.29
• Formule: C₁₄H₁₆N₂O₄
• Couleur/Forme: Yellow
• InChI: InChI=1S/C14H16N2O4/c17-11-5-6-12(18)15(11)9-3-1-2-4-10-16-13(19)7-8-14(16)20/h5-8H,1-4,9-10H2
• Code InChI: InChIKey=PYVHLZLQVWXBDZ-UHFFFAOYSA-N
• SMILES: O=C1C=CC(=O)N1CCCCCCN1C(=O)C=CC1=O