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B103004

Sigma-Aldrich

N-Butylurea

99%

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About This Item

Linear Formula:
CH3(CH2)3NHCONH2
CAS Number:
Molecular Weight:
116.16
Beilstein:
1744775
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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.
H Chang et al.
Blood, 61(4), 693-704 (1983-04-01)
Fifteen compounds reported to be inhibitors of gelation or sickling were studied by standard methods. These tests included (1) the determination of the solubility of deoxyhemoglobin S or Csat, (2) evaluation of sickling in whole SS blood at various pO2s
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
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

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