Skip to Content
Merck
CN

633267

Dicyclohexylcarbodiimide solution

60 wt. % in xylenes

Synonym(s):

N,N′-Methanetetraylbis[cyclohexanamine], DCC, NSC 30022, NSC 53373, NSC 57182

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C13H22N2
CAS Number:
538-75-0
Molecular Weight:
206.33
NACRES:
NA.22
PubChem Substance ID:
329759830
UNSPSC Code:
12352200
MDL number:
MFCD00011659

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Dicyclohexylcarbodiimide solution, 60 wt. % in xylenes

InChI

1S/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2

SMILES string

C1CCC(CC1)N=C=NC2CCCCC2

InChI key

QOSSAOTZNIDXMA-UHFFFAOYSA-N

reaction suitability

reaction type: Coupling Reactions

concentration

60 wt. % in xylenes

refractive index

n20/D 1.503

density

0.898 g/mL at 25 °C

Application

Catalyst for Mitsunobu reaction to synthesize tetramethylpyrazine derivatives

Coupling agent for generation of graphene and graphene oxide sheets supported on silica

Endophytic bacterium L14 biomass inhibitor

Used to produce:
  • Multifunctional aqueous nanocrystals stabilized by hyperbranched polyglycerol
  • MnO2 nanosheets attached to Au nanoparticles on carbon nantubes
  • Functionalized single-walled carbon nantotube arrays

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Inhalation - STOT SE 3

target_organs

Central nervous system,Liver,Kidney, Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

86.0 °F

flash_point_c

30 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000114907
0000114906
0000109056
0000091921
0000050162

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Siobhan P Brown et al.
American heart journal, 169(3), 334-341 (2015-03-03)
The Resuscitation Outcomes Consortium is conducting a randomized trial comparing survival with hospital discharge after continuous chest compressions without interruption for ventilation versus currently recommended American Heart Association cardiopulmonary resuscitation with interrupted chest compressions in adult patients with out-of-hospital cardiac
Marc Aprahamian et al.
Chembiochem : a European journal of chemical biology, 12(5), 777-783 (2011-03-04)
Myo-inositol trispyrophosphate (ITPP), a synthetic allosteric effector of hemoglobin, increases the regulated oxygen-releasing capacity of red blood cells (RBCs), leading to suppression of hypoxia-inducible factor 1α (HIF-1α) and to down-regulation of hypoxia-inducible genes such as vascular endothelial growth factor (VEGF).
Andreia Biolo et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(6), 1926-1929 (2009-02-11)
A major determinant of maximal exercise capacity is the delivery of oxygen to exercising muscles. myo-Inositol trispyrophosphate (ITPP) is a recently identified membrane-permeant molecule that causes allosteric regulation of Hb oxygen binding affinity. In normal mice, i.p. administration of ITPP
Kenji Mizutani et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(33), 13474-13479 (2011-08-05)
The prokaryotic V-ATPase of Enterococcus hirae, closely related to the eukaryotic enzymes, provides a unique opportunity to study the ion-translocation mechanism because it transports Na(+), which can be detected by radioisotope (22Na(+)) experiments and X-ray crystallography. In this study, we
Daniel P Keeley et al.
Developmental cell, 54(1), 60-74 (2020-06-26)
Basement membranes (BMs) are supramolecular matrices built on laminin and type IV collagen networks that provide structural and signaling support to tissues. BM complexity, however, has hindered an understanding of its formation, dynamics, and regulation. Using genome editing, we tagged
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service