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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:
Assay:
99%
Form:
crystals
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Quality Level

assay

99%

form

crystals

mp

95-98 °C (lit.)

SMILES string

CCCCNC(N)=O

InChI

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

InChI key

CNWSQCLBDWYLAN-UHFFFAOYSA-N



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
Srinivasan R Nagarajan et al.
Bioorganic & medicinal chemistry, 11(22), 4769-4777 (2003-10-15)
The human immunodeficiency virus (HIV) has been shown to be the causative agent for AIDS. The HIV virus encodes for a unique aspartyl protease that is essential for the production of enzymes and proteins in the final stages of maturation.
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



Global Trade Item Number

SKUGTIN
B103004-100G04061832492070