Basic information Safety Supplier Related

Dibutylurea

Basic information Safety Supplier Related

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
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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)
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Safety Information

Safety Statements 
24/25

MSDS

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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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