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10580-52-6

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10580-52-6 Usage

Description

Vanadium(II) chloride, also known as vanadium dichloride, is a chemical compound with the formula VCl2. It is characterized by its apple green color and forms hexagonal plate-like structures. Vanadium(II) chloride is a strong reducing agent, which makes it useful in various chemical reactions and processes.
Source:
Vanadium(II) chloride can be prepared by heating vanadium trichloride (VCl3) in a nitrogen (N2) atmosphere, followed by sublimation in the same N2 atmosphere.

Uses

Used in Chemical Synthesis:
Vanadium(II) chloride is used as a reducing agent in various chemical synthesis processes due to its strong reducing properties. It can facilitate the conversion of other compounds and participate in important reactions.
Used in Purification of Hydrochloric Acid:
Vanadium(II) chloride is used as a purifying agent for hydrochloric acid (HCl). It is particularly effective in removing arsenic impurities from the acid, which is crucial for maintaining the purity and quality of the HCl.
Used in Chemical Research:
Due to its unique chemical properties, vanadium(II) chloride is also utilized in research and development for studying various chemical reactions and processes. It can provide valuable insights into the behavior of different compounds and help develop new synthetic methods or improve existing ones.
Used in Industrial Applications:
Vanadium(II) chloride may also find applications in specific industrial processes where its strong reducing properties are required. These applications can vary depending on the needs of the industry and the specific reactions or processes involved.

Check Digit Verification of cas no

The CAS Registry Mumber 10580-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10580-52:
(7*1)+(6*0)+(5*5)+(4*8)+(3*0)+(2*5)+(1*2)=76
76 % 10 = 6
So 10580-52-6 is a valid CAS Registry Number.
InChI:InChI=1/3ClH.V/h3*1H;/q;;;+3/p-3

10580-52-6 Well-known Company Product Price

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  • Aldrich

  • (422371)  Vanadium(II)chloride  85%

  • 10580-52-6

  • 422371-1G

  • 768.69CNY

  • Detail
  • Aldrich

  • (422371)  Vanadium(II)chloride  85%

  • 10580-52-6

  • 422371-5G

  • 2,658.24CNY

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10580-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dichlorovanadium

1.2 Other means of identification

Product number -
Other names vanadium 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:10580-52-6 SDS

10580-52-6Upstream product

10580-52-6Downstream Products

10580-52-6Relevant articles and documents

Reduction of dinitrobenzenes by electron-carrying catalysts in the electrosynthesis of diaminobenzenes

Abakumov, M. V.,Leonova, M. Yu.,Mikhalchenko, L. V.,Novikov, V. T.,Zaplavin, A. P.

, p. 1927 - 1933 (2021/11/05)

The interaction of isomeric dinitrobenzenes (DNBs) with titanium(III), tin(II), and vanadium(II) chlorides, which are reducing agents used as electron carriers in the electrosynthesis of diaminobenzenes, has been studied. Rate constants of the reduction of isomeric DNBs and nitrophenylhydroxylamines by SnCl2 and TiCl3 in a 2 M water-alcohol solution (10 vol.% C2H5OH) of HCl were measured, and activation energies of the reduction of isomeric DNBs were determined. The rates of interaction of DNBs with the listed mediators increase in the series SnCl2 3 2. It is shown that the electrolysis of DNBs in the presence of an excess of these mediators makes it possible to obtain the corresponding diaminobenzenes with a yield of 60–90%.

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