Pralidoxime (chloride)
For Laboratory Research Only. Not for Clinical or Personal Use.
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Pralidoxime (chloride)
Description :
Pralidoxime chloride is a potent reactivator of acetylcholinesterase (AChE) . Pralidoxime chloride reactivates nerve agent-inhibited AChE via direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent. Pralidoxime chloride is an antidote for organophosphate poisoning[1][2].CAS Number :
[51-15-0]Product Name Alternative :
2-PAM chlorideUNSPSC :
12352005Hazard Statement :
H302, H315, H319, H335Target :
Cholinesterase (ChE)Type :
Reference compoundRelated Pathways :
Neuronal SignalingApplications :
Neuroscience-NeuromodulationField of Research :
Neurological DiseaseAssay Protocol :
https://www.medchemexpress.com/Pralidoxime-chloride.htmlConcentration :
10mMPurity :
99.83Solubility :
DMSO : 21.67 mg/mL (ultrasonic) |H2O : ≥ 100 mg/mLSmiles :
C[N+]1=CC=CC=C1/C=N/O.[Cl-]Molecular Formula :
C7H9ClN2OMolecular Weight :
172.61Precautions :
H302, H315, H319, H335References & Citations :
[1]Cadieux CL, et al. Probing the activity of a non-oxime reactivator for acetylcholinesterase inhibited by organophosphorus nerve agents. Chem Biol Interact. 2016;259 (Pt B) :133‐141.|[2]Eyer P, Buckley N. Pralidoxime for organophosphate poisoning. Lancet. 2006;368 (9553) :2110‐2111.|[3]Houzé P, et al. High Dose of Pralidoxime Reverses Paraoxon-Induced Respiratory Toxicity in Mice. Turk J Anaesthesiol Reanim. 2018;46 (2) :131‐138.Shipping Conditions :
Room TemperatureStorage Conditions :
4°C (Powder, sealed storage, away from moisture)Scientific Category :
Reference compound1Clinical Information :
LaunchedIsoform :
AChE

