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4-Methylmorpholine N-oxide solution_Molecular_structure_CAS_7529-22-8)
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4-Methylmorpholine N-oxide solution

Catalog No. 67874 Name Sigma Aldrich
CAS Number 7529-22-8 Website http://www.sigmaaldrich.com
M. F. C5H11NO2 Telephone 1-800-521-8956
M. W. 117.14634 Fax
Purity Email
Storage Chembase ID: 128514

SYNONYMS

Title
4-甲基吗啡-N-氧化物 溶液
IUPAC name
4-methylmorpholin-4-ium-4-olate
IUPAC Traditional name
N-methylmorpholine N-oxide
Synonyms
NMO solution
NSC 73198
NMMO solution
NMO 溶液
NSC 82153

DATABASE IDS

MDL Number MFCD00005947
CAS Number 7529-22-8
PubChem SID 24885452

PROPERTIES

Concentration ~50% in H2O
Empirical Formula (Hill Notation) C5H11NO2
Grade technical
Refractive Index n20/D 1.43
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
German water hazard class 1

DETAILS

Description (English)
Application
Oxidant for synthesis of novel organic polymer - inorganic hybrid for use as a catalyst for asymmetrical epoxidation1Reagent or Reactant for:
• Cyclocondensation and cyclization in the enantioselective synthesis of oxazolomycin A2
• Wharton rearrangement and stereoselective dihydroxylation reactions3
• Reduction of amine N-oxides by diboron reagents4
• Synthesis of polysaccharide blend fibers5
• Synthesis of cellulose / modified nano-SiO2 composite packaging films6
• Copper-catalyzed oxidative coupling for preparation of propargylamines7Used as a pretreatment for techno-economical study of ethanol and biogas production from spruce wood8
Description (简体中文)
Application
Oxidant for synthesis of novel organic polymer - inorganic hybrid for use as a catalyst for asymmetrical epoxidation1Reagent or Reactant for:
• Cyclocondensation and cyclization in the enantioselective synthesis of oxazolomycin A2
• Wharton rearrangement and stereoselective dihydroxylation reactions3
• Reduction of amine N-oxides by diboron reagents4
• Synthesis of polysaccharide blend fibers5
• Synthesis of cellulose / modified nano-SiO2 composite packaging films6
• Copper-catalyzed oxidative coupling for preparation of propargylamines7Used as a pretreatment for techno-economical study of ethanol and biogas production from spruce wood8

REFERENCES