DIPHENYLCARBAZONE
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
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)
- form
- Powder
- pka
- 9.83±0.43(Predicted)
- 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)
Safety Information
- Risk Statements
- 22-36/37/38
- Safety Statements
- 22-24/25-36/37/39-26
- RIDADR
- 1325
- WGK Germany
- 3
- RTECS
- LQ9420000
- F
- 10-21
- TSCA
- Yes
- HS Code
- 29280000
MSDS
- Language:English Provider:SigmaAldrich
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.]
DIPHENYLCARBAZONESupplier
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