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D80800

N,N′-Dicyclohexylurea

Name: <I>N</I>,<I>N</I>′-Dicyclohexylurea
Brand: ALDRICH

98%

Synonym(s):

1,3-Dicyclohexylurea

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About This Item

Linear Formula:

C₆H₁₁NHCONHC₆H₁₁

CAS Number:

2387-23-7

Molecular Weight:

224.34

NACRES:

NA.22

PubChem Substance ID:

24894186

UNSPSC Code:

12352100

EC Number:

219-213-7

MDL number:

MFCD00003829

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

232-233 °C (lit.)

SMILES string

O=C(NC1CCCCC1)NC2CCCCC2

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)

InChI key

ADFXKUOMJKEIND-UHFFFAOYSA-N

Gene Information

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

Description

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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Certificates of Analysis (COA)

Lot/Batch Number

0000456251

0000451647

0000441211

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The solid state structure and reactivity of NbCl(5) x (N,N'-dicyclohexylurea) in solution: evidence for co-ordinated urea dehydration to the relevant carbodiimide.

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

Oral delivery of 1,3-dicyclohexylurea nanosuspension enhances exposure and lowers blood pressure in hypertensive rats.

Sarbani Ghosh et al.

Basic & clinical pharmacology & toxicology, 102(5), 453-458 (2008-03-04)

Cytochrome P450-derived epoxyeicosatrienoic acids (EET) are biologically active metabolites of arachidonic acid that have potent effects on renal vascular reactivity and tubular ion transport and have been implicated in the control of blood pressure. EETs are hydrolyzed to their less

Rapid determination of soluble epoxide hydrolase inhibitors in rat hepatic microsomes by high-performance liquid chromatography with electrospray tandem mass spectrometry.

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

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Global Trade Item Number

SKU	GTIN
D80800-25G	04061833589199