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4-Ethylmorpholine, 98%, Thermo Scientific Chemicals
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Catalog number A11905.AP
also known as A11905-AP
Price (USD)/ Each
50.20
-
Quantity:
500 mL
Price (USD)/ Each
50.20
4-Ethylmorpholine, 98%, Thermo Scientific Chemicals
Catalog numberA11905.AP
Price (USD)/ Each
50.20
-
Chemical Identifiers
CAS100-74-3
IUPAC Name4-ethylmorpholine
Molecular FormulaC6H13NO
InChI KeyHVCNXQOWACZAFN-UHFFFAOYSA-N
SMILESCCN1CCOCC1
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Specifications
Specification Sheet
Specification SheetIdentification (FTIR)Conforms
Refractive Index1.4395-1.4435 @ 20°C
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥97.5%
N-Ethylmorpholine is a component of the buffer used in basic peptide separation through anion-exchange chromatography. Further, it acts as a catalyst in the preparation of polyurethane foam.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
N-Ethylmorpholine is a component of the buffer used in basic peptide separation through anion-exchange chromatography. Further, it acts as a catalyst in the preparation of polyurethane foam.
Solubility
Miscible with water.
Notes
Light and air sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agents.
N-Ethylmorpholine is a component of the buffer used in basic peptide separation through anion-exchange chromatography. Further, it acts as a catalyst in the preparation of polyurethane foam.
Solubility
Miscible with water.
Notes
Light and air sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Base for use in peptide and similar coupling reactions. For example, has been used in conjunction with ethyl chloroformate for the mild coupling of substituted aromatic acids with primary amines or for the coupling of N-hydroxysuccinimide active esters with peptide residues: J. Med. Chem., 34, 2328 (1991). Compare 4-Methyl morpholine, A12158. For peptide reagents, see Appendix 6.
- Shen, C.; Wang, P.; Beves, J. E. New ruthenium(II) complexes of 2, 2': 6', 2″-terpyridine derivatives as supramolecular building blocks. Polyhedron 2016, 103, 241-247.
- Samide, M. J.; Smith, G. D. Analysis and quantitation of volatile organic compounds emitted from plastics used in museum construction by evolved gas analysis-gas chromatography-mass spectrometry. J. Chromatogr. A 2015, 1426, 201-208.