Other grades of this product :
| Diphenyl sulfide Basic information |
| Diphenyl sulfide Chemical Properties |
| Melting point | -40 °C (lit.) | | Boiling point | 296 °C (lit.) | | density | 1.113 g/mL at 20 °C (lit.) | | vapor pressure | 0.01 hPa (25 °C) | | refractive index | n20/D 1.6327(lit.) | | Fp | >230 °F | | storage temp. | Store below +30°C. | | solubility | Soluble in ether, benzene, carbon disulphide. | | form | Liquid | | color | Clear colorless to light yellow | | Water Solubility | insoluble | | Sensitive | Stench | | Merck | 14,7314 | | BRN | 1907932 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | InChIKey | LTYMSROWYAPPGB-UHFFFAOYSA-N | | LogP | 4.63 at 20℃ | | CAS DataBase Reference | 139-66-2(CAS DataBase Reference) | | NIST Chemistry Reference | Diphenyl sulfide(139-66-2) | | EPA Substance Registry System | Diphenyl sulfide (139-66-2) |
| Hazard Codes | Xn,N | | Risk Statements | 22-38-50/53-36/38 | | Safety Statements | 23-28-60-61-37/39-26 | | RIDADR | UN 3082 9/PG 3 | | WGK Germany | 3 | | RTECS | SX2275000 | | F | 13 | | Hazard Note | Harmful/Stench | | TSCA | Yes | | HS Code | 2930 90 98 | | HazardClass | 6.1 | | PackingGroup | III | | Toxicity | LD50 orally in rats: 0.49 ml/kg (Smyth) |
| Diphenyl sulfide Usage And Synthesis |
| Chemical Properties | colourless liquid | | Uses | Diphenyl Sulfide is an aromatic organosulfur compound. Diphenyl Sulfide is metabolite of the fungicide Edifenphos as well as a potential Impurity of Fenticonazole Nitrate (F279250). | | Uses | Diphenyl sulfide is used as a raw material for triaryl sulfonium photoinitiator, intermediates for agrichemicals, catalyst, metal extractants. | | Definition | ChEBI: An aryl sulfide that consists of two phenyl groups connected by a sulphur atom. | | Synthesis Reference(s) | Chemical and Pharmaceutical Bulletin, 35, p. 1770, 1987 DOI: 10.1248/cpb.35.1770 | | Flammability and Explosibility | Notclassified | | Purification Methods | Wash the sulfide with aqueous 5% NaOH, then water. Dry it with CaCl2, then with sodium. The sodium is filtered off, and the diphenyl sulfide is distiiled under reduced pressure. [Beilstein 2 H 299, 6 IV 1488.] |
| Diphenyl sulfide Preparation Products And Raw materials |
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