Dibutylurea
Dibutylurea Basic information
- Product Name:
- Dibutylurea
- Synonyms:
-
- 1,3-DIBUTYLUREA
- n,n’-dibutylurea(asimpurity)
- Urea, N,N'-dibutyl-
- urea,1,3-dibutyl-
- N,N'-DI-N-BUTYLUREA
- N,N'-DIBUTYLUREA
- TIMTEC-BB SBB007953
- Dibutylurea,98%
- CAS:
- 1792-17-2
- MF:
- C9H20N2O
- MW:
- 172.27
- EINECS:
- 217-258-7
- Product Categories:
-
- Agro-Products, Aliphatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
- Mol File:
- 1792-17-2.mol
Dibutylurea Chemical Properties
- Melting point:
- 65-75 °C
- Boiling point:
- 115°C 0,03mm
- Density
- 0.9845 (rough estimate)
- refractive index
- 1.5800 (estimate)
- Flash point:
- 115°C/0.03mm
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 14.44±0.46(Predicted)
- color
- White to Off-White
- BRN
- 1704165
- CAS DataBase Reference
- 1792-17-2(CAS DataBase Reference)
- NIST Chemistry Reference
- 1,3-Dibutylurea(1792-17-2)
- EPA Substance Registry System
- N,N'-Dibutylurea (1792-17-2)
Safety Information
- Safety Statements
- 24/25
MSDS
- Language:English Provider:1,3-Dibutylurea
- Language:English Provider:ACROS
- Language:English Provider:ALFA
Dibutylurea Usage And Synthesis
Chemical Properties
white to pink or light beige crystalline powder
Uses
N,N'-Dibutylurea is a degradation product of Benomyl, the active ingredient in Benlate fungicides.
Uses
N,N''-Dibutylurea is a degradation product of Benomyl, the active ingredient in Benlate fungicides.
Preparation
The reactions under CO2 pressured conditions were carried out in a stainless steel reactor (SUS 304, 30 mL, TVS-5 type). Thus, butylamine (2.9 g, 40 mmol), Ph3SbO (370 mg, 1.0 mmol), P4S10 (890 mg, 2.0 mmol), and benzene (20 mL) were charged into the reactor, and then CO2 was introduced at a pressure of 4.9 MPa (50 kg cm-2, ca. 65 mmol) at room temperature. The reactor was heated at 80 ℃ in a temperature-regulated incubator for 12 h. When a reaction temperature higher than 100 ℃ was necessary, an oil bath was used. After the heating, the reactor was cooled and carefully decompressed. The contents were treated with hot benzene (3×20 mL) and filtered to remove an insoluble residue containing the catalyst and phosphoric acid derivatives. The collected benzene solution was then concentrated to dryness in vacuo with cooling. Pure 1,3-dibutylurea was isolated by recrystallization from ligroin (yield 2.99 g, 88%).
Synthesis Reference(s)
Synthetic Communications, 21, p. 1923, 1991 DOI: 10.1080/00397919108021783
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Dibutylurea(1792-17-2)Related Product Information
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- TOLBUTAMIDE
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- Dibutyltin dilaurate
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- Diethyl dibutylmalonate
- Butylated Hydroxytoluene
- n-Butyllithium
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- BIUREA
- 1,5-Diphenylcarbazide
- Tetrabutylurea
- Lenacil
- 1,1'-CARBONYLDIPIPERIDINE
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