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2051-24-3

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2051-24-3 Usage

Description

DECACHLOROBIPHENYL, also known as a polychlorobiphenyl, is a compound in which all the hydrogen atoms in a biphenyl molecule are replaced by chlorine atoms. This chemical structure gives it unique properties and potential applications in various industries.

Uses

Used in Chemical Industry:
DECACHLOROBIPHENYL is used as a chemical intermediate for the production of various chemicals and materials. Its high chlorine content makes it a valuable component in the synthesis of other compounds.
Used in Plastics Industry:
In the plastics industry, DECACHLOROBIPHENYL is used as an additive to enhance the flame retardancy and thermal stability of plastic materials. Its chlorine content contributes to the fire-resistant properties of the final product.
Used in Electrical Industry:
DECACHLOROBIPHENYL is utilized as an insulating material in the electrical industry due to its high resistance to heat and electrical breakdown. It is particularly useful in high-voltage applications where insulation is critical.
Used in Environmental Remediation:
DECACHLOROBIPHENYL can be employed in environmental remediation processes, such as soil and water treatment, to remove or neutralize harmful contaminants. Its chemical properties allow it to interact with and immobilize pollutants, reducing their impact on the environment.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DECACHLOROBIPHENYL may be used as a starting material for the synthesis of various drugs, particularly those with antimicrobial, antifungal, or antiviral properties. Its unique structure can be modified to create new therapeutic compounds.
Please note that the provided materials do not include specific applications for DECACHLOROBIPHENYL, so the uses listed above are inferred based on the general properties of polychlorinated biphenyls and their potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2051-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2051-24:
(6*2)+(5*0)+(4*5)+(3*1)+(2*2)+(1*4)=43
43 % 10 = 3
So 2051-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C12Cl10/c13-3-1(4(14)8(18)11(21)7(3)17)2-5(15)9(19)12(22)10(20)6(2)16

2051-24-3 Well-known Company Product Price

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  • Supelco

  • (48318)  Decachlorobiphenylsolution  certified reference material, 200 μg/mL in acetone

  • 2051-24-3

  • 000000000000048318

  • 266.76CNY

  • Detail
  • Cerilliant

  • (SCD-015)  Decachlorobiphenyl  99%, vial of 1 g, analytical standard

  • 2051-24-3

  • SCD-015-1G

  • 1,974.96CNY

  • Detail

2051-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name decachlorobiphenyl

1.2 Other means of identification

Product number -
Other names Decachlorobiphenyl solution

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:2051-24-3 SDS

2051-24-3Relevant articles and documents

Optimization of Perchlorination Conditions for Some Representative Polychlorinated Biphenyls

Lin, Jia Ming,Hee, Shane S, Que

, p. 2130 - 2134 (1985)

The yield of decachlorobiphenyl (DCB) from representative Aroclors (50 to 6000 ng) using antimony pentachloride as perchlorinating agent was extremely temperature dependent below 236 deg C for a reaction period of 2 h.At 288 deg C, a 35-min reaction period was sufficient to obtain DCB yields >80percent for Aroclors 1016, 1242, 1254, and 1268.The perchlorination process was shown to be first order.The temperature dependence of the reaction times below 236 deg C was largely responsible for the inconsistent perchlorination yields reported previously in the literature.The extraction of DCB with hexane form a HCl-acidified perchlorinated solution and the subsequent column chromatography on silica gel were also essential after the perchlorination to quantitate the DCB by (63)Ni electron capture/gas chromatography.The structures of the two nonachlorobiphenyls, which were the penultimate stable intermediates before DCB, were found.The methodology to use the technique for air and blood samples was described.

Electrophilic phosphonium cations (EPCs) with perchlorinated-aryl substituents: Towards air-stable phosphorus-based Lewis acid catalysts

Postle, Shawn,Podgorny, Vitali,Stephan, Douglas W.

, p. 14651 - 14657 (2016/10/03)

A series of phosphines incorporating (C6Cl5) substituents, Ph2P(C6Cl5) 1, PhP(C6Cl5)22, P(C6Cl5)33 and (C6F5)P(C6Cl5)24 were prepared. In the case of 1, 2 and 4, these were converted to the corresponding aryl-difluorophosphoranes 5-7via reaction with XeF2, whereas reaction of 3 with XeF2 afforded only an inseparable mixture of products. The compounds 5-7 were converted to the fluorophosphonium cations 8-10, whereas the reaction of 3 with Selectfluor afforded (C6Cl5)2POF and (C6Cl5)2. The fluorophosphonium salts showed evidence of improved air stability as well as Lewis acid catalytic activity in hydrodefluorination, hydrosilylation, deoxygenation and dehydrocoupling chemistry.

Effects of oxygen on formation of PCB and PCDD/F on extracted fly ash in the presence of carbon and cupric salt

Pekarek,Grabic,Marklund,Puncochar,Ullrich

, p. 777 - 782 (2007/10/03)

The effect of oxygen-nitrogen atmosphere (N2 + 10%O2, N2 + 1%O2 and 99.999% N2) on the formation of PCB, PCDD and PCDF by the de novo synthetic reactions in the system consisting of extracted fly ash

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