15093-47-7

Basic information

• Product Name: 1,1-dibutyl-3-phenylthiourea
• CAS NO: 15093-47-7
• Molecular Formula: C₁₅H₂₄N₂S
• Molecular Weight: 264.4295
• Mol File: 15093-47-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 353°C at 760 mmHg
• Flash Point: 167.3°C
• Density: 1.044g/cm³
• Vapor Pressure: 3.69E-05mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: 1,1-dibutyl-3-phenylthiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dibutyl-3-phenylthiourea(15093-47-7)
• EPA Substance Registry System: 1,1-dibutyl-3-phenylthiourea(15093-47-7)

Safety Data

• Hazardous Substances Data: 15093-47-7(Hazardous Substances Data)

Usage

Type of compound

Thiourea derivative

Butyl group

Attached to both nitrogen atoms

Phenyl group

Attached to the central carbon atom

Common use

Rubber accelerator

Function in rubber industry

Increases vulcanization, making rubber stronger and more durable

Potential medicinal properties

Antioxidant effects
Anti-inflammatory effects

Health hazards

Toxic and harmful if ingested or inhaled

Safety concerns

Proper handling and usage required to avoid health risks

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 111-92-2 dibutylamine 
• 75-15-0 carbon disulfide 
• 62-53-3 aniline 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 

Downstream Products

• 15927-04-5 N¹,N¹-Di-n-butyl-N²-phenylchlorformamidin 
• 93162-49-3 N,N-Dibutyl-N'-phenyl-S-methyl-isothioharnstoff 
• 144749-78-0 bromo(N,N-dibutyl-N'-phenylthiourea-S)bis(triphenylphosphine-P)copper(I) 
• 144749-77-9 {Cu(P(C₆H₅)3)2(C₆H₅NHC(S)N((CH₂)3CH₃)2)Cl} 
• 144749-79-1 {Cu(P(C₆H₅)3)2(C₆H₅NHC(S)N((CH₂)3CH₃)2)I} 
• 78363-38-9 Cu[C₆H₅NC(S)N(C₄H₉)2]2 
• 263237-06-5 [Cu(triphenylstibine)(N,N-dibutyl-N'-phenylthiourea)2Cl] 
• 263237-08-7 [Cu(triphenylstibine)(N,N-dibutyl-N'-phenylthiourea)2I] 
• 263237-07-6 [Cu(triphenylstibine)(N,N-dibutyl-N'-phenylthiourea)2Br] 
• 168977-42-2 [Cu(As(C₆H₅)3)2(C₆H₅NHC(S)N(C₄H₉)2)Br] 
• 168977-41-1 [Cu(As(C₆H₅)3)2(C₆H₅NHC(S)N(C₄H₉)2)Cl] 
• 168977-43-3 [Cu(As(C₆H₅)3)2(C₆H₅NHC(S)N(C₄H₉)2)I] 
• 1237747-22-6 N-phenyl-N-((E)-(phenylimino)(dibutylamin-1-yl)methyl)dibutylamine-1-carbothioamide 

Relevant articles and documents

Thiourea derivatives, simple in structure but efficient enzyme inhibitors and mercury sensors

In this study six unsymmetrical thiourea derivatives, 1-isobutyl-3-cyclohexylthiourea (1), 1-tert-butyl-3-cyclohexylthiourea (2), 1-(3-chlorophenyl)-3-cyclohexylthiourea (3), 1-(1,1-dibutyl)-3-phenylthiourea (4), 1-(2-chlorophenyl)-3-phenylthiourea (5) an

Cerium ammonium nitrate-catalyzed aerobic oxidative coupling of dithiocarbamates: Facile synthesis of thioureas and bis(aminothiocarbonyl)disulfides

Diverse disubstituted and trisubstituted thioureas were synthesized by the condensation of dithiocarbamate TEA (or DABCO) salts and amines using cerium ammonium nitrate (CAN) as a catalyst in high yields at room temperature. It is a one-pot method and it is unnecessary to isolate isothiocyanates. This reaction probably took place through nucleophilic addition of amines to isothiocyanates, which were generated by oxidative coupling of dithiocarbamates and the following decomposition of bis(aminothiocarbonyl)disulfides. When secondary amines and CS2served as the reactants, bis(aminothiocarbonyl)disulfides were obtained via tandem nucleophilic addition/oxidative coupling reactions in moderate to excellent yields. In all the coupling reactions, the oxidant was air and CAN possibly acted as an SET catalyst.