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1,2-Diphenylhydrazine

1,2-Diphenylhydrazine

100 Onwards INR

Product Details:

  • Usage It does not evaporate easily but may be released to air when attached to dust particles. 1,2-Diphenylhydrazine is a man-made chemical that was used in the past to make benzidine which was used to make various fabric dyes. Benzidine dyes are no longer used in the United States, but may still be used in other countries.
  • Melting Point 19.5 C
  • Molecular Weight 108.14 Grams (g)
  • Molecular Formula C6H8N2
  • Purity 98%
  • Supply Ability : 500 , , Kilograms Per Month
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Price And Quantity

  • 100 Onwards INR
  • 1 , , Kilograms

Product Specifications

  • C6H8N2
  • 98%
  • It does not evaporate easily but may be released to air when attached to dust particles. 1,2-Diphenylhydrazine is a man-made chemical that was used in the past to make benzidine which was used to make various fabric dyes. Benzidine dyes are no longer used in the United States, but may still be used in other countries.
  • 19.5 C
  • 108.14 Grams (g)

Trade Information

  • Cash Advance (CA), Cash in Advance (CID)
  • 500 , , Kilograms Per Month
  • 2-8 Week
  • Yes
  • Sample costs shipping and taxes has to be paid by the buyer
  • Carton and Poly Bag.
  • Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • All India

Product Description

1,2-Diphenylhydrazine

Analytical standard, ampule of 100 mg

Synonym: N,N-Diphenylhydrazine, N,N-Bianiline, Hydrazobenzene, NSC 3510

  • CAS Number 122-66-7

  • Linear Formula C6H5NHNHC6H5

  • Molecular Weight 184.24

grade   analytical standard
form   neat
packaging   ampule of 100 mg
application(s)   HPLC: suitable
  gas chromatography (GC): suitable
mp   123-126 C(lit.)
format   neat

Application

Reactant involved in:
 Insertion reactions with organometallic tantalum complexes[]
 Reduction reactions catalyzed by titanium(III) trichloride yielding amines[]
 Studying the mechanism of hydrazobenzene rearrangement[]
 Reaction with N-heterocyclic stable silylene[]
 Synthesis of dimanganese amide hydrazide cluster complexes[]
 Iron-mediated hydrazine reductions yielding iron arylimide cubanes[]

 

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