InChI key
OFYLBLSSPQTTHT-VMPITWQZSA-N
InChI
1S/C6H6N2O/c9-8-5-6-1-3-7-4-2-6/h1-5,9H/b8-5+
SMILES string
[H]\C(=N\O)c1ccncc1
assay
98%
mp
130-133 °C (lit.)
Application
4-Pyridinealdoxime was used in the chromatographic separation and NMR characterization of the isomers of 1,1′-Methylenebis{4-[(hydroxyimino)methyl]pyridinium) dichloride.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
G R Veera Babu et al.
Archives internationales de physiologie et de biochimie, 97(2), 205-209 (1989-04-01)
Effects in vitro of benthiocarb on rat brain Mg2+-ATPase were studied to elucidate the interaction of benthiocarb with Mg2+-ATPase. Based on IC50 values, it was evident that Mg2+-ATPase was sensitive to benthiocarb. Non-competitive inhibition with respect to activation by ATP
Tsung-Ming Shih et al.
Archives of toxicology, 83(12), 1083-1089 (2009-09-19)
Methoxime (MMB-4) is a leading candidate oxime acetylcholinesterase (AChE) reactivator to replace pralidoxime (2-PAM) for therapeutic treatment of nerve agent intoxication. 4-Pyridine aldoxime (4-PA) is a synthetic starting material, a breakdown product, and a probable metabolite of MMB-4. There is
Patrick Macauley et al.
Journal of pharmaceutical and biomedical analysis, 49(4), 889-894 (2009-02-17)
1,1'-Methylenebis{4-[(hydroxyimino)methyl]pyridinium) dichloride (MMB-4), a promising antidote for organophosphate poisoning, has been shown by chromatography and NMR to be a mixture of geometric isomers, predominantly the E/E form. The chromatographically separated isomers have been isolated, directly characterized by NMR to be
[Capillary isotachophoresis--a new method in drug analysis. 4. Analytic capillary tachophoresis of obidoxime and pyridine-4-aldoxime].
R Jannasch
Die Pharmazie, 41(7), 511-512 (1986-07-01)
Aditya Kapil Valiveti et al.
Chemico-biological interactions, 237, 125-132 (2015-06-14)
A series of mono pyridinium oximes linked with arenylacetamides as side chains were synthesized and their in vitro reactivation potential was evaluated against human acetylcholinesterase (hAChE) inhibited by organophosphorus inhibitors (OP) such as sarin, VX and tabun. The reactivation data
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