1,3-Diphenylurea

1,3-Diphenylurea
Names
	Preferred IUPAC name N,N′-Diphenylurea
	Other names 1,3-Diphenylurea; Diphenylurea; carbanilide
Identifiers
CAS Number	102-07-8 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	782650
ChEBI	CHEBI:41320;
ChEMBL	ChEMBL354676;
ChemSpider	7314;
DrugBank	DB07496;
ECHA InfoCard	100.002.731
EC Number	203-003-7;
Gmelin Reference	143821
PubChem CID	7595;
UNII	94YD8RMX5B ;
CompTox Dashboard (EPA)	DTXSID2025183 ;
	InChI InChI=1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16) Key: GWEHVDNNLFDJLR-UHFFFAOYSA-N;
	SMILES c1ccc(cc1)N/C(=N\c2ccccc2)/O;
Properties
Chemical formula	C13H12N2O
Molar mass	212.252 g·mol−1
Magnetic susceptibility (χ)	-127.5·10−6 cm3/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H312, H332
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

1,3-Diphenylurea is a phenyl urea-type compound with the formula (PhNH)₂CO (Ph = C₆H₅). It is a colorless solid that is prepared by transamidation of urea with aniline.

DPU is a cytokinin, a type of plant hormone that induces flower development. It occurs in coconut milk.^[1] The cytokinin effect of DPU is relatively low, but other more potent phenylurea-type cytokinins have been reported.^[2]

References

^ Shantz, E. M.; Steward, F. C. (1955). "The Identification of Compound A from Coconut Milk as 1,3-Diphenylurea". Journal of the American Chemical Society. 77 (23): 6351. doi:10.1021/ja01628a079.
^ Effect of cytokinin-active phenylurea derivatives on shoot multiplication. T. Genkov and I. Ivanova, Bulg. J. Plant Physiol., 1995, 21(1), pages 73–83 (link to article at researchgate)

External links

The dictionary definition of Diphenylurea at Wiktionary

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[1] Shantz, E. M.; Steward, F. C. (1955). "The Identification of Compound A from Coconut Milk as 1,3-Diphenylurea". Journal of the American Chemical Society. 77 (23): 6351. doi:10.1021/ja01628a079.

[2] Effect of cytokinin-active phenylurea derivatives on shoot multiplication. T. Genkov and I. Ivanova, Bulg. J. Plant Physiol., 1995, 21(1), pages 73–83 (link to article at researchgate)

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