Phenidone

Phenidone
Names


IUPAC name 1-phenyl-3-pyrazolidinone
Identifiers
CAS Number	92-43-3^Y
3D model (Jmol)	Interactive image
ChemSpider	6823^Y
ECHA InfoCard	100.001.960
EC Number	202-155-1
PubChem CID	7090
InChI InChI=1S/C9H10N2O/c12-9-6-7-11(10-9)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,12)^Y Key: CMCWWLVWPDLCRM-UHFFFAOYSA-N^Y InChI=1/C9H10N2O/c12-9-6-7-11(10-9)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,12) Key: CMCWWLVWPDLCRM-UHFFFAOYAF
SMILES O=C2NN(c1ccccc1)CC2
Properties
Chemical formula	C₉H₁₀N₂O
Molar mass	162.19 g·mol⁻¹
Appearance	Crystal leaflets or needles
Melting point	121 °C (250 °F; 394 K)
Solubility in water	10 g/100 ml at 100 °C
Solubility in ethanol	10 g/100 ml (hot)
Solubility in diethyl ether	practically insoluble
Hazards
Main hazards	Harmful if swallowed
Safety data sheet	External MSDS
R-phrases (outdated)	R20 R22
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y (what is ^YN ?)
Infobox references

Phenidone (1-phenyl-3-pyrazolidinone) is an organic compound that is primarily used as a photographic developer. It has five to ten times the developing power as Metol. It also has low toxicity and, unlike some other developers, does not cause dermatitis upon skin contact.

Phenidone is Ilford's trademark for this material, which was first prepared in 1890. It was not until 1940 that J. D. Kendall, in the laboratories of Ilford Limited, discovered the reducing properties of this compound. Large scale production did not become feasible until 1951.

Phenidone functions as a reducing agent. It converts to the N-phenyl-hydroxypyrazole:

Phenidone can be prepared by heating phenyl hydrazine with 3-chloropropanoic acid.

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