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633267

Dicyclohexylcarbodiimide solution

60 wt. % in xylenes

Synonym(s):

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

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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
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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

SMILES string

C1CCC(CC1)N=C=NC2CCCCC2

InChI

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

InChI key

QOSSAOTZNIDXMA-UHFFFAOYSA-N

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

flash_point_f

86.0 °F

flash_point_c

30 °C

ppe

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000114907
0000114906
0000109056
0000091921
0000050162

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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
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Global Trade Item Number

SKUGTIN
633267-100ML04061832721576
633267-800ML04061838128430