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C106402

Sigma-Aldrich

N-Cyclohexyl-N′-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate

95%

Synonym(s):

4-[2-[(Cyclohexylcarbonimidoyl)amino]ethyl]-4-methylmorpholinium p-toluenesulfonate, N-Cyclohexyl-N′-(β-[N-methylmorpholino]ethyl)carbodiimide p-toluenesulfonate salt, CMC, CMC metho-p-toluenesulfonate, Morpho CDI

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About This Item

Empirical Formula (Hill Notation):
C14H26N3O · C7H7O3S
CAS Number:
2491-17-0
Molecular Weight:
423.57
EC Number:
219-650-3
MDL number:
MFCD00011979
UNSPSC Code:
12352111
PubChem Substance ID:
329774842
NACRES:
NA.26

Quality Level

200

Assay

95%

form

crystals

mp

113-115 °C (lit.)

SMILES string

Cc1ccc(cc1)S([O-])(=O)=O.C[N+]2(CCOCC2)CCN=C=NC3CCCCC3

InChI

1S/C14H26N3O.C7H8O3S/c1-17(9-11-18-12-10-17)8-7-15-13-16-14-5-3-2-4-6-14;1-6-2-4-7(5-3-6)11(8,9)10/h14H,2-12H2,1H3;2-5H,1H3,(H,8,9,10)/q+1;/p-1

InChI key

GBCAVSYHPPARHX-UHFFFAOYSA-M

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Application

Employed in a facile sequencing technique for pseudouridylate residues in RNA.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A Bakin et al.
Biochemistry, 32(37), 9754-9762 (1993-09-21)
A new technique has been developed for the facile location of pseudouridylate (psi) residues in any RNA molecule. The method uses two known modification procedures which in combination uniquely identify U residues which have been converted into psi. The first
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Malaria journal, 17(1), 370-370 (2018-10-20)
Plasmodium vivax is the most geographically widespread of the human malaria parasites, causing 50,000 to 100,000 deaths annually. Plasmodium vivax parasites have the unique feature of forming dormant liver stages (hypnozoites) that can reactivate weeks or months after a parasite-infected
W A Ziehler et al.
Current protocols in nucleic acid chemistry, Chapter 6, Unit 6-Unit 6 (2008-04-23)
This unit provides thorough coverage of the most useful chemical and enzyme probes that can be used to examine RNA secondary and tertiary structure. Footprinting methods are presented using dimethyl sulfate, diethyl pyrocarbonate, ethylnitrosourea, kethoxal, CMCT, and nucleases. For chemical
Jinghui Song et al.
Nature chemical biology, 16(2), 160-169 (2019-12-11)
Pseudouridine synthases (PUSs) are responsible for installation of pseudouridine (Ψ) modification in RNA. However, the activity and function of the PUS enzymes remain largely unexplored. Here we focus on human PUS10 and find that it co-expresses with the microprocessor (DROSHA-DGCR8
P V Sergiev et al.
Journal of molecular biology, 299(2), 379-389 (2000-06-22)
The proximity of loop D of 5 S rRNA to two regions of 23 S rRNA, domain II involved in translocation and domain V involved in peptide bond formation, is known from previous cross-linking experiments. Here, we have used site-directed
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