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Merck
CN

B103004

N-Butylurea

99%

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About This Item

Linear Formula:
CH3(CH2)3NHCONH2
CAS Number:
Molecular Weight:
116.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-748-4
Beilstein/REAXYS Number:
1744775
MDL number:
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Product Name

N-Butylurea, 99%

InChI

1S/C5H12N2O/c1-2-3-4-7-5(6)8/h2-4H2,1H3,(H3,6,7,8)

InChI key

CNWSQCLBDWYLAN-UHFFFAOYSA-N

SMILES string

CCCCNC(N)=O

assay

99%

form

crystals

mp

95-98 °C (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Joanna Krakowiak et al.
Journal of biological physics, 45(2), 161-172 (2019-03-25)
The results of thermal studies of denaturation of hen egg white lysozyme (HEWL) in water and an aqueous solution of N-butylurea (BU) are presented. High-precision densimetric measurements were used to characterize and analyze the changes of the specific volume, v
Peter L Larsen et al.
Journal of the American Chemical Society, 126(21), 6522-6523 (2004-05-27)
Metal complexes with terminal chalcogenido ligands are known for the early transition-metal complexes, yet for the heavier congeners (e.g., sulfido and selenido), there are no analogous examples for the late 3d metal ions. Reported herein is the isolation and characterization
Kevin X Chen et al.
Bioorganic & medicinal chemistry, 16(4), 1874-1883 (2007-11-23)
Starting from a pentapeptide Hepatitis C virus NS3 protease inhibitor, a number of alpha-ketoamide inhibitors based on novel dichlorocyclopropylproline P2 core were synthesized and investigated for their HCV NS3 serine protease activity. The key intermediate 3,4-dichlorocyclopropylproline was obtained through a
Thermodynamics of anti-sickling agents with hemoglobin S.
R C Benedict et al.
Journal of molecular biology, 150(3), 423-434 (1981-08-15)
Taiho Park et al.
Journal of the American Chemical Society, 127(51), 18133-18142 (2005-12-22)
An exceptionally strong quadruply hydrogen-bonded complex is formed between 2,7-diamido-1,8-naphthyridine 3 (DAN) and the butylurea of guanosine 6 (UG) in chloroform. The UG unit can be prepared in four steps from guanosine on a 10 g scale in excellent yields

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