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DIPHENYLCARBAZONE

Basic information Safety Supplier Related

DIPHENYLCARBAZONE Basic information

Product Name:
DIPHENYLCARBAZONE
Synonyms:
  • Diphenylcarbazone Compound with s-Diphenylcarbazide, Reagent
  • (E)-1,5-diphenylcarbazone
  • 1-Phenyl-2-[hydroxy(phenylazo)methylene]hydrazine
  • PhenylazoforMic acid 2-phenylhydrazide, suitable for coloriMetric analysis 10GR
  • (contains Diphenylcarbazide)
  • Diphenylcarbazone 
  • Diphenylcarbazone, for analysis
  • 1,5-DIPHENYLCARBAZONE
CAS:
538-62-5
MF:
C13H12N4O
MW:
240.26
EINECS:
208-698-0
Product Categories:
  • Pharmaceutical Intermediates
  • Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
Mol File:
538-62-5.mol
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DIPHENYLCARBAZONE Chemical Properties

Melting point:
119-123 °C(lit.)
Boiling point:
382.98°C (rough estimate)
Density 
1.19±0.1 g/cm3 (20 ºC 760 Torr)
refractive index 
1.6120 (estimate)
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
9.83±0.43(Predicted)
form 
Powder
color 
Orange
Water Solubility 
Soluble in acetone. Insoluble in water.
Merck 
14,3322
CAS DataBase Reference
538-62-5(CAS DataBase Reference)
EPA Substance Registry System
Diazenecarboxylic acid, phenyl-, 2-phenylhydrazide (538-62-5)
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Safety Information

Risk Statements 
22-36/37/38
Safety Statements 
22-24/25-36/37/39-26
RIDADR 
1325
WGK Germany 
3
RTECS 
LQ9420000
10-21
TSCA 
Yes
HS Code 
29280000

MSDS

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DIPHENYLCARBAZONE Usage And Synthesis

Chemical Properties

orange powder

Uses

Indicator

Uses

It is a reagent for mercury determination.

Uses

As a sensitive reagent for Hg, with which it gives a blue color.

Purification Methods

It crystallises from EtOH (ca 5mL/g), and dry the orange-red needles at 50o. A commercial sample, nominally sym-diphenylcarbazone (m 154-156o) was a mixture of diphenylcarbazide and diphenylcarbazone. The former was removed by dissolving 5g of the crude material in 75mL of warm EtOH, then adding 25g Na2CO3 dissolved in 400mL of distilled water. The alkaline solution was cooled and extracted six times with 50mL portions of diethyl ether (discarded). Diphenylcarbazone was then precipitated by acidifying the alkaline solution with 3M HNO3 or glacial acetic acid. It was filtered off, air dried, and stored in the dark [Gerlach & Frazier Anal Chem 30 1142 1958]. Other impurities are phenylsemicarbazide and diphenylcarbodiazone. Impurities can be detected by chromatography [Willems et al. Anal Chim Acta 51 544 1970]. It is used for detection and estimation of Hg, Zn, Cd, Cr, Cu, Fe and Mo [Cheng et al. Handbook of Organic Analytical Reagents, Boca Baton 277 1982, Beilstein 16 H 24, 16 IV 17.]

DIPHENYLCARBAZONE Preparation Products And Raw materials

Raw materials

DIPHENYLCARBAZONESupplier

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