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Merck
CN

D80800

N,N′-Dicyclohexylurea

98%

Synonym(s):

1,3-Dicyclohexylurea

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About This Item

Linear Formula:
C6H11NHCONHC6H11
CAS Number:
Molecular Weight:
224.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-213-7
MDL number:
Assay:
98%
Form:
solid
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InChI key

ADFXKUOMJKEIND-UHFFFAOYSA-N

InChI

1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)

SMILES string

O=C(NC1CCCCC1)NC2CCCCC2

assay

98%

form

solid

mp

232-233 °C (lit.)

Quality Level

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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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T Watanabe et al.
Analytical biochemistry, 299(2), 227-234 (2001-12-04)
A rapid and reliable electrospray tandem mass spectrometric method for soluble epoxide hydrolase (sEH) inhibitors in rat hepatic microsomes is described. Four synthesized sEH inhibitors were extracted from rat hepatic microsomes with ethyl acetate and were determined by HPLC using
Michele Aresta et al.
Dalton transactions (Cambridge, England : 2003), 39(30), 6985-6992 (2010-06-15)
NbCl(5) x (N,N'-dicyclohexylurea) 1a owns a distorted octahedral structure due to intramolecular NH...Cl bonding. The unit cell contains four units which are intermolecularly NH...Cl and NH...N bonded. An extended intramolecular network of H-bonding (N-H...Cl, CH...Cl, CH...N) causes the 3D self
Z Yu et al.
Circulation research, 87(11), 992-998 (2000-11-25)
The cytochrome P450-derived epoxyeicosatrienoic acids (EETs) have potent effects on renal vascular reactivity and tubular sodium and water transport; however, the role of these eicosanoids in the pathogenesis of hypertension is controversial. The current study examined the hydrolysis of the
L Mark Hall et al.
Journal of chemical information and modeling, 52(5), 1222-1237 (2012-04-12)
The goal of many metabolomic studies is to identify the molecular structure of endogenous molecules that are differentially expressed among sampled or treatment groups. The identified compounds can then be used to gain an understanding of disease mechanisms. Unfortunately, despite
Julian Dominik Wolf et al.
Journal of colloid and interface science, 566, 234-241 (2020-02-02)
Lysine based cationic surfactants are well-tolerated tools for hydrophobic ion pairing (HIP) with DNA and its incorporation into lipophilic delivery systems. Di-Boc-lysine was esterified with 1-hexadecanol and the Boc-residues were cleaved off resulting in hexadecyl lysinate (HL). Subsequently, its Log

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