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ChemicalBook--->CAS DataBase List--->112241-19-7

112241-19-7

112241-19-7 Structure

112241-19-7 Structure
IdentificationBack Directory
[Name]

4-succinimidyloxycarbonyl-alpha-methyl-alpha(2-pyridyldithio)toluene
[CAS]

112241-19-7
[Synonyms]

4-Succinimidyloxycarbonyl-α-Methyl-α-(2-Pyridyldithio)toluene
2,5-Dioxopyrrolidin-1-yl 4-[1-(pyridin-2-yldisulfanyl)ethyl]benzoate
4-succinimidyloxycarbonyl-alpha-methyl-alpha(2-pyridyldithio)toluene
2,5-dioxopyrrolidin-1-yl 4-(1-(pyridin-2-yldisulfaneyl)ethyl)benzoate
Benzoic acid, 4-[1-(2-pyridinyldithio)ethyl]-, 2,5-dioxo-1-pyrrolidinyl ester
[Molecular Formula]

C18H16N2O4S2
[MDL Number]

MFCD00083161
[MOL File]

112241-19-7.mol
[Molecular Weight]

388.46
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

Light yellow to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[General Description]

SMPT is a heterobifunctional sulfhydryl- and amine-reactive cross-linker. SMPT is used often for conjugating a toxin molecule to a monoclonal antibody directed against a cell-surface antigen. These immunotoxins produced with SMPT are highly potent as the cleavable disulfide imparts increased cytotoxicity compared to conjugates without a cleavable bond, such as those produced with SPDP. Also, next to the pyridine-2-thione in the spacer arm are a benzene ring and a methyl group adjacent to a carbon that hinders the disulfide bond, allowing exceptional conjugate stability in vivo. SMPT has the added benefit of being more stable to hydrolysis in aqueous solutions than other NHS cross-linkers.
[reaction suitability]

reagent type: cross-linking reagent
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