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1,1'-DIPHENYL-4,4'-BIPYRIDINIUM DICHLORIDE, commonly known as paraquat, is a highly toxic chemical compound that serves as a non-selective herbicide. It is capable of killing a broad spectrum of plants and plant parts upon contact. Paraquat is notorious for its extreme toxicity to both humans and animals, with even minimal ingestion potentially leading to severe injury or death. Due to these hazardous properties, its use is heavily regulated and restricted in numerous countries. Additionally, it poses health risks such as lung damage when inhaled and skin irritation upon contact.

47369-00-6

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47369-00-6 Usage

Uses

Used in Agricultural Industry:
1,1'-DIPHENYL-4,4'-BIPYRIDINIUM DICHLORIDE is used as a herbicide for its ability to effectively control and eliminate a wide range of unwanted plant species. Its non-selective nature makes it a potent tool in agricultural settings for managing and eradicating invasive or undesirable vegetation.
However, it is important to note that due to the high toxicity of 1,1'-DIPHENYL-4,4'-BIPYRIDINIUM DICHLORIDE, its application in the agricultural industry is subject to stringent regulations and safety measures to minimize the risk of exposure to humans, animals, and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 47369-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,3,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 47369-00:
(7*4)+(6*7)+(5*3)+(4*6)+(3*9)+(2*0)+(1*0)=136
136 % 10 = 6
So 47369-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H34N2/c1-3-7-21(8-4-1)23-15-11-19(12-16-23)20-13-17-24(18-14-20)22-9-5-2-6-10-22/h1,3-4,7-8,19-20,22H,2,5-6,9-18H2

47369-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4-(1-phenylpyridin-1-ium-4-yl)pyridin-1-ium,dichloride

1.2 Other means of identification

Product number -
Other names N,N'-diphenyl-4,4'-bipyridylium dichloride

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:47369-00-6 SDS

47369-00-6Relevant academic research and scientific papers

A new class of light-fast oxonol dyes: Organic-glass forming salts of oxonol anions and 4,4′-bipyridinium cations

Inagaki, Yoshio,Morishima, Shin-Ichi,Wariishi, Koji,Saito, Naoki,Akiba, Masaharu

, p. 345 - 347 (2006)

A new class of light-fast oxonol dyes were prepared. These dyes were spin-coated onto glass plates using 2,2,3,3-tetrafluoro-1-propanol as a solvent to form noncrystalline-solid-dye films. They were colored, transparent, uniform, but dark when placed between crossed polarizers. The change of the normalized absorbance of dye films measured at their respective absorption maxima. The oxidative quenching mechanism is responsible for the light-fastness of the oxonol salts. The heavy-metal free and organic recording dyes with enhanced light-resistance will expand the range of potential applications for oxonol dyes.

Anion-induced ionic liquid crystals of diphenylviologens

Wang, Ren-Tzong,Lee, Gene-Hsiang,Lai, Chung K.

, p. 9430 - 9444 (2018/09/25)

Two series of ionic liquid crystals derived from diphenylviologens, 1 and 2, were prepared and their photophysical and electrochemical properties were also investigated. The crystallographic data of two single crystals, 1-RSO3 (n = 10) and 2-BF

Redox Photochromism of Arylviologen Crystals

Kamogawa, Hiroyoshi,Sato, Shigeki

, p. 321 - 323 (2007/10/02)

Reversible color development induced by near UV light (photochromism) was observed for some crystalline powder of 1,1'-diaryl-4,4'-bipyridinium bis(p-toluenesulfonate).Redox mechanism by the electron transfer from the sulfonate anion to viologen dication

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