P60205
2-Pyridinealdoxime methiodide
99%
Synonym(s):
2-PAM, 2-PAM iodide, Pralidoxime iodide
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25 G
$261.00
About This Item
Empirical Formula (Hill Notation):
C7H11IN2O
CAS Number:
Molecular Weight:
266.08
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Kevin G McGarry et al.
Toxicological sciences : an official journal of the Society of Toxicology, 174(1), 124-132 (2019-12-28)
Organophosphorus (OP) compounds, which include insecticides and chemical warfare nerve agents (CWNAs) such as sarin (GB) and VX, continue to be a global threat to both civilian and military populations. It is widely accepted that cholinesterase inhibition is the primary
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Organophosphate (OP) threat agents can trigger seizures that progress to status epilepticus, resulting in persistent neuropathology and cognitive deficits in humans and preclinical models. However, it remains unclear whether patients who do not show overt seizure behavior develop neurological consequences.
Qiqi Zheng et al.
Analytica chimica acta, 982, 78-83 (2017-07-25)
An electrochemical method based on non-enzymatic inhibition for the determination of organophosphorus pesticide (OPPs) using pralidoxime chloride (PAM-Cl) as a universal electrochemical probe was reported. Cyclic voltammetry was performed to characterize the redox properties of pralidoxime and OPPs. Differential pulse
Kimberly D Spradling et al.
Journal of neuroinflammation, 8, 84-84 (2011-07-23)
Although the acute toxicity of organophosphorus nerve agents is known to result from acetylcholinesterase inhibition, the molecular mechanisms involved in the development of neuropathology following nerve agent-induced seizure are not well understood. To help determine these pathways, we previously used
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