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1,3-Diphenyl-2-thiourea

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CAS:102-08-9
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CAS:102-08-9
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CAS:102-08-9
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CAS:102-08-9
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Products Intro: Product Name:1,3-Diphenyl-2-thiourea
CAS:102-08-9
Purity:99% Package:1KG;1USD

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  • 1,3-Diphenyl-2-thiourea
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  • $0.00 / 25KG
  • 2023-09-06
  • CAS:102-08-9
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  • Purity: 99%
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1,3-Diphenyl-2-thiourea Basic information
Product Name:1,3-Diphenyl-2-thiourea
Synonyms:N,N-Diphenylsulfourea;N,N'-Diphenylthiocaramide;N,N'-Diphenylthiocarbamide;1,3-diphenyl-2-thio-ure;2-Fenylotiomocznik;a-1 Thiocarbanilide;Activit;Akrochem thio No. 1
CAS:102-08-9
MF:C13H12N2S
MW:228.31
EINECS:203-004-2
Product Categories:
Mol File:102-08-9.mol
1,3-Diphenyl-2-thiourea Structure
1,3-Diphenyl-2-thiourea Chemical Properties
Melting point 152-155 °C(lit.)
Boiling point 50℃
density 1.32
vapor pressure 0.001Pa at 25℃
refractive index 1.5700 (estimate)
storage temp. Store below +30°C.
pka12.68±0.70(Predicted)
form Crystalline Powder
color White to pale yellow
Water Solubility <0.01 g/100 mL at 19 ºC
Merck 14,3333
BRN 644277
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKeyFCSHMCFRCYZTRQ-UHFFFAOYSA-N
LogP3.6
CAS DataBase Reference102-08-9(CAS DataBase Reference)
NIST Chemistry ReferenceThiourea, n,n'-diphenyl-(102-08-9)
EPA Substance Registry SystemDiphenylthiourea (102-08-9)
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 36/37/39-45-24/25
RIDADR UN 2811 6.1/PG 2
WGK Germany 3
RTECS FE1225000
TSCA Yes
HazardClass 6.1
PackingGroup II
HS Code 29309070
Hazardous Substances Data102-08-9(Hazardous Substances Data)
ToxicityMLD orally in rabbits: 1.5 g/kg (Hanzlik, Irvine)
MSDS Information
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1,3-Diphenyl-2-thiourea English
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1,3-Diphenyl-2-thiourea Usage And Synthesis
DescriptionDiphenylthiourea is a rubber chemical used as an accelerator and stabilizer in neopren.
Chemical Propertieswhite powder
UsesVulcanizing accelerator; sulfur dyes.
UsesN,N'-Diphenylthiourea possesses a wide dipole moment and thus is involved in the forming wide metal chelated complexes as the radioactive-compound which used in radiopharmaceutical imaging, and to treat metal poisoning. It is used in co-crystals development used in the field of nonlinear optics to generate new coherent wavelengths.
UsesN,N'-Diphenylthiourea is a vulcanizing accelerator; sulfur dyes; pharmaceutieals; floatation agent; acid inhibitor; intermediate for organic synthesis; accelerator and activator for chloroprene rubber and ethylene-propylene-diene terpolymers; as heat stabilizer in PVC adhesive-tape backing.
DefinitionChEBI: N,N'-diphenylthiourea is thiourea in which each nitrogen carries a phenyl substituent. It has a role as an allergen.
Synthesis Reference(s)Tetrahedron Letters, 15, p. 1191, 1974 DOI: 10.1016/S0040-4039(01)82442-4
General DescriptionWhite to off-white powder.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileAn organosulfide amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Health HazardACUTE/CHRONIC HAZARDS: When heated to decomposition 1,3-Diphenyl-2-thiourea emits highly toxic fumes.
Fire HazardFlash point data for 1,3-Diphenyl-2-thiourea are not available. 1,3-Diphenyl-2-thiourea is probably combustible.
Flammability and ExplosibilityNon flammable
Industrial usesThiocarbanilide (diphenyl thiourea) is a crystalline compound, only marginally soluble in water. In solution, it can assume a tautomeric form, typical of thiocarbanilide.
The first tautomer has acidic characteristics. The hydrogen can easily react with cations from the mineral surface and therefore can act as a collector. The second form (II) does not have collecting properties. Thiocarbanilide is a very effective and selective collector for galena. Diphenylthiocarbazide (C6H5–NH–NH)2–C=S. This collector also appears in two forms; in the active form the hydrogen is connected to sulfur. This reagent can be both anionic and cationic. This collector can be utilized for flotation of nickel and cobalt minerals after treatment of the pulp with copper sulfate.
Contact allergensIt is a rubber chemical used as an accelerator and stabilizing agent in neoprene
Safety ProfileModerately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits highly toxic fumes of SOx, and NOx,.
Purification MethodsCrystallise the thiourea from boiling EtOH by adding hot water and allowing to cool. [Beilstein 12 H 394, 12 IV 810.]
Tag:1,3-Diphenyl-2-thiourea(102-08-9) Related Product Information
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