Spin Traps

Cat.No. Product Name Information

GC42351 4-carboxy TEMPO

4-Carboxyl-2,2,6,6-tetramethylpiperidin-1-oxyl

4-carboxy TEMPO is a nitroxide and spin label. 4-carboxy TEMPO Chemical Structure

GC41397 BMPO

BocMPO

BMPO is a cell-permeable superior spin trap that captures OH and O₂^•−, forming stable BMPO/OH and ^•BMPO-OOH adducts. BMPO Chemical Structure

GC43352 CYPMPO

RR 071

CYPMPO is a free radical spin trap with excellent trapping capabilities toward hydroxyl and superoxide radicals in biological and chemical systems.

GC43411 DEPMPO-biotin DEPMPO is a nitrone that is used to spin trap reactive O-, N-, S-, and C-centered radicals and allow their characterization when used in association with electron spin resonance. DEPMPO-biotin Chemical Structure

GC41290 EMPO

5-(Ethoxycarbonyl)-5-methyl-1-Pyrroline-N-Oxide

EMPO is a hydrophilic cyclic nitrone analog of the free radical spin trap DMPO.

GC44408 Nitrosobenzene

NSC 66479

Nitrosobenzene is a spin trap that has been used in the study of oxidative DNA damage and nitroso-compound-induced respiratory burst in neutrophils. Nitrosobenzene Chemical Structure

GC44666 POBN

4-POBN

POBN is a cell permeable, hydrophilic spin trap that can be used to detect free radical adducts in in vitro studies. POBN Chemical Structure

GC44773 PTIO

αPhenyltetramethylnitronyl nitroxide

PTIO is a nitric oxide-selective capture agent that can react with nitric oxide to form the corresponding ^•NO₂ and imino nitroxides. PTIO Chemical Structure

GC45010 TEMPONE

4oxoTEMPO, Triacetoneamine nitroxide

2,2,6,6-Tetramethylpiperidin-1-oxyl (TEMPO) is a stable radical that will react with reactive oxygen species (ROS). TEMPONE Chemical Structure

Products for Spin Traps