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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 effect of baicalein-loaded Y-shaped miktoarm copolymer on spatial memory and hippocampal expression of DHCR24, SELADIN and SIRT6 genes in rat model of Alzheimer.

Mozhgan Aghajanzadeh et al.

International journal of pharmaceutics, 586, 119546-119546 (2020-06-17)

In the present study, we successfully synthesized nanocarriers (NCs) based on Y-shaped miktoarm copolymers, Poly Ethylene Glycol-Lysine-(Poly Caprolactone)2 (PEG-Lys-PCL2), which were loaded by baicalein (B) through the nanoprecipitation process to assess their in-vitro and in-vivo properties. We applied various methods

14,15-Dihydroxyeicosatrienoic acid activates peroxisome proliferator-activated receptor-alpha.

Xiang Fang et al.

American journal of physiology. Heart and circulatory physiology, 290(1), H55-H63 (2005-08-23)

Epoxyeicosatrienoic acids (EETs), lipid mediators synthesized from arachidonic acid by cytochrome P-450 epoxygenases, are converted by soluble epoxide hydrolase (SEH) to the corresponding dihydroxyeicosatrienoic acids (DHETs). Originally considered as inactive degradation products of EETs, DHETs have biological activity in some

Design, synthesis and evaluation of non-urea inhibitors of soluble epoxide hydrolase.

Stevan Pecic et al.

Bioorganic & medicinal chemistry letters, 22(1), 601-605 (2011-11-15)

Inhibition of soluble epoxide hydrolase (sEH) has been proposed as a new pharmaceutical approach for treating hypertension and vascular inflammation. The most potent sEH inhibitors reported in literature to date are urea derivatives. However, these compounds have limited pharmacokinetic profiles.

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Global Trade Item Number

SKU	GTIN
D80800-25G	04061833589199