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

• Catalog No.: C1011
• CAS Number: 2491-17-0
• M. F.: C21H33N3O4S
• M. W.: 423.56942
• Purity: ≥97% (CHN)

SYNONYMS

• IUPAC name: 4-{2-[(N-cyclohexylcarboximidoyl)amino]ethyl}-4-methylmorpholin-4-ium 4-methylbenzene-1-sulfonate
• IUPAC Traditional name: 4-[2-(N-cyclohexylcarboximidoylamino)ethyl]-4-methylmorpholin-4-ium tosylate
• Synonyms: CME-CDI; N-Cyclohexyl-N′-(β-[N-methylmorpholino]ethyl)carbodiimide p-toluenesulfonate; CMC

DATABASE IDS

• EC Number: 219-650-3
• Beilstein Number: 3872192
• PubChem SID: 24892296
• MDL Number: MFCD00011979
• CAS Number: 2491-17-0

PROPERTIES

• Empirical Formula (Hill Notation): C14H26N3O · C7H7O3S
• Purity: ≥97% (CHN)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• Storage Temperature: -20°C
• German water hazard class: 3

DETAILS

Description (English)

Application
Water-soluble condensing reagent for peptide synthesis, reagent used for coupling ligands to carriers in affinity chromatography.
Biochem/physiol Actions
N-Cyclohexyl-N′-(2-morpholinoethyl)carbodiimide (CMCT) selectively modifies/derivitizes all pseudouridine, thiouridine and 2-methylthio-6-isopentenyladenosine nucleosides for detection by methods such as matrix-assisted laser desorption/ionization mass spectrometry. CMCT, a water-soluble condensing reagent for peptide synthesis, is used as a reagent for coupling ligands to carriers in affinity chromatography.

Description (简体中文)

Application
Water-soluble condensing reagent for peptide synthesis, reagent used for coupling ligands to carriers in affinity chromatography.