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36913-39-0

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36913-39-0 Usage

Uses

Different sources of media describe the Uses of 36913-39-0 differently. You can refer to the following data:
1. Dopaminergic neurotoxin; a selective cytostatic agent in small-cell lung cancer cell lines with neuroendocrine properties.
2. MPP+ iodide is an active metabolite of the dopaminergic neurotoxin MPTP.

General Description

1-Methyl-4-phenylpyridinium (MPP+) induces neurotoxicity by inhibiting mitochondrial redox functions in the striatal synaptosomes. It is a potential neurotoxin and induces Parkinson′s disease in animal models. It mediates apoptosis by the generation of reactive oxygen species in cerebellar granule neurons and neuroblastoma cells. MPP+ modulates the distribution of dopamine. It elicits neurotoxicity by activating neuronal nitric oxide synthase (nNOS), resulting in excess nitric oxide.

Biochem/physiol Actions

MPP+ iodide is an active metabolite of dopaminergic neurotoxin MPTP.

Check Digit Verification of cas no

The CAS Registry Mumber 36913-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,1 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36913-39:
(7*3)+(6*6)+(5*9)+(4*1)+(3*3)+(2*3)+(1*9)=130
130 % 10 = 0
So 36913-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9N.HI/c1-2-4-10(5-3-1)11-6-8-12-9-7-11;/h1-9H;1H

36913-39-0 Well-known Company Product Price

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  • Sigma

  • (D048)  MPP+ iodide  ≥98% (HPLC), powder

  • 36913-39-0

  • D048-100MG

  • 1,655.55CNY

  • Detail
  • Sigma

  • (D048)  MPP+ iodide  ≥98% (HPLC), powder

  • 36913-39-0

  • D048-1G

  • 9,921.60CNY

  • Detail

36913-39-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-4-phenylpyridinium iodide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36913-39-0 SDS

36913-39-0Relevant articles and documents

Cation-π interactions secure aggregation induced emission of planar organic luminophores

Leduskrasts, Kaspars,Kinens, Artis,Suna, Edgars

, p. 12663 - 12666 (2019)

The use of non-covalent intermolecular π+-π interactions between quaternary pyridinium or imidazolium cations and aromatic π systems is an efficient approach to achieve AIE in planar purely organic luminophores.

MATERIALS FOR USE IN AN AQUEOUS ORGANIC REDOX FLOW BATTERY

-

Paragraph 0256; 0260, (2018/05/15)

Described herein are aqueous organic redox flow batteries that include a first redox active material that can include a metallocene or a salt thereof, and a second redox active material that can include a viologen or a salt thereof. The aqueous organic re

Photophysical and electrochemical properties of platinum(ii) complexes bearing a chromophore-acceptor dyad and their photocatalytic hydrogen evolution

Zhang, Gui-Ju,Gan, Xin,Xu, Quan-Qing,Chen, Yong,Zhao, Xi-Juan,Qin, Biao,Lv, Xiao-Jun,Lai, Siu-Wai,Fu, Wen-Fu,Che, Chi-Ming

experimental part, p. 8421 - 8429 (2012/07/30)

A series of platinum(ii) complexes bearing a chromophore-acceptor dyad obtained by reacting 4-(p-bromomethylphenyl)-6-phenyl-2,2′-bipyridine or 4′-(p-bromomethylphenyl)-2,2′:6′,2′′-terpyridine with pyridine, 4-phenylpyridine, 4,4′-bipyridine, 1-methyl-4-(

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