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15721-02-5

15721-02-5 Structure

15721-02-5 Structure
IdentificationMore
[Name]

2,2',5,5'-Tetrachlorobenzidine
[CAS]

15721-02-5
[Synonyms]

2,2',5,5'-TETRACHLOROBENZIDINE
4,4'-DIAMINO-2,2',5,5'-TETRACHLOROBIPHENYL
1’-biphenyl)-4,4’-diamine,2,2’,5,5’-tetrachloro-(
1’-biphenyl]-4,4’-diamine,2,2’,5,5’-tetrachloro-[
2,2’,5,5’-tetrachloro-4,4’-diaminodiphenyl
2,2’,5,5’-tetrachloro-benzidin
3,3’,6,6’-tetrachlorobenzidine
4,4'-diamino-5,5',2,2'-tetrachlorobiphenyl
2,2,5,5-TETRACHLORO-4,4-DIAMINOBIPHENYL
2,2,5,5-TETRACHLOROBENZIDINE 98+%
2,2',5,5'-Tetrachloro-[1,1'-Biphenyl]-4,4'-diamine
TCB
2,2',5,5'-Tetrachlorobenzidine
2,2',5,5'-Tetrachlorobiphenyl-4,4'-diamine
[EINECS(EC#)]

239-815-3
[Molecular Formula]

C12H8Cl4N2
[MDL Number]

MFCD00043918
[Molecular Weight]

322.02
[MOL File]

15721-02-5.mol
Chemical PropertiesBack Directory
[Melting point ]

135-140 °C(lit.)
[Boiling point ]

477.67°C (rough estimate)
[density ]

1.5309 (rough estimate)
[refractive index ]

1.6000 (estimate)
[storage temp. ]

-70°C
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

1.58±0.13(Predicted)
[color ]

Light yellow to Yellow to Orange
[biological source]

human
[Water Solubility ]

water: soluble
[CAS DataBase Reference]

15721-02-5(CAS DataBase Reference)
[IARC]

3 (Vol. 27, Sup 7) 1987
[EPA Substance Registry System]

15721-02-5(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

61
[Safety Statements ]

53-45
[WGK Germany ]

3
[RTECS ]

DD1751000
[TSCA ]

TSCA listed
[HS Code ]

2921.59.8090
[Safety Profile]

Suspected carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits very toxic fumes of NO, and Cl-.
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

Pigment Yellow 81
Hazard InformationBack Directory
[Uses]

PKM1active human has been used in:
  • cell-based kinase assay to study the ability of a compound to inhibit the kinase activity of PKM1.
  • oxidative stress experiments on PKM2.
  • Co-immunoprecipitation (Co-IP) to determine pyruvate kinase M2 (PKM2) as a novel direct binding partner of phosphoserine aminotransferase 1 (PSAT1).
[Definition]

ChEBI: 2,2',5,5'-Tetrachlorobenzidine is a member of biphenyls and a dichlorobenzene.
[Production Methods]

2,2' ,5,5' -Tetrachlorobenzidine is made by the reduction of 2,5-dichloronitrobenzene with zinc dust and sodium hydroxide solution. The subsequent rearrangement is carried out using sulfuric acid or hydrochloric acid. The dihydrochloride melts at 230 ℃. Tetrachlorobenzidine is marketed as the free base and is used to produce yellow pigments.
[Biological Activity]

Pyruvate kinase (PK) catalyzes the dephosphorylation of phosphoenolpyruvate(PEP) into pyruvate. It is also involved in glycolysis by releasing ATP.Allosteric effects and intracellular signal transduction regulate the enzymaticactivity of PKM1. PKM1 is involved in several biological processes such asmetabolic reprogrammingand innate and acquired immune response. Itparticipates in protein interactionsprotein synthesisglycolysisandintranuclear signal transduction.
Spectrum DetailBack Directory
[Spectrum Detail]

2,2',5,5'-Tetrachlorobenzidine(15721-02-5)MS
2,2',5,5'-Tetrachlorobenzidine(15721-02-5)1HNMR
2,2',5,5'-Tetrachlorobenzidine(15721-02-5)13CNMR
2,2',5,5'-Tetrachlorobenzidine(15721-02-5)IR1
2,2',5,5'-Tetrachlorobenzidine(15721-02-5)IR2
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

2,2',5,5'-Tetrachlorobenzidine,>98.0%(T)(15721-02-5)
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