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4-Methylmorpholine N-oxide - 50 wt. % in H2O, high purity , CAS No.7529-22-8

16 Citations

COA

Grade & Purity:

50 wt. % in H2O

Cas Number: 7529-22-8
Molecular Weight: 117.15
Beilstein Registry Number: 507437
EC Number: 231-391-8
MDL number: MFCD00005947
PubChem CID: 82029

In stock

Item Number

M105979

Grouped product items
SKU	Size	Availability	Price
M105979-25ml	25ml	3	$12.90
M105979-100ml	100ml	5	$29.90
M105979-500ml	500ml	3	$104.90

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Morpholines (127) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms	4-methylmorpholin-4-ium-4-olate \| Clopononum \| M2192 \| N-methymorpholine N-oxide \| 4-Methylmorpholine Oxide \| N-methyl-morpholine N-oxide \| N-Methylmorpholine N-oxide \| 4-methyl morpholine N-oxide \| 4-Methylmorpholine N-oxide, 97% \| BP-30197 \| 4-Methylmor
Specifications & Purity	50 wt. % in H2O
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Oxidant for synthesis of novel organic polymer - inorganic hybrid for use as a catalyst for asymmetrical epoxidation. Reagent or Reactant for: Cyclocondensation and cyclization in the enantioselective synthesis of oxazolomycin A. Wharton rearrangement and stereoselective dihydroxylation reactions. Reduction of amine N-oxides by diboron reagents. Synthesis of polysaccharide blend fibers. Synthesis of cellulose / modified nano-SiO2 composite packaging films. Copper-catalyzed oxidative coupling for preparation of propargylamines. Used as a pretreatment for techno-economical study of ethanol and biogas production from spruce wood.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Oxazinanes
    - Subclass Morpholines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Oxazinanes
Subclass	Morpholines
Intermediate Tree Nodes	Not available
Direct Parent	Morpholines
Alternative Parents	Trialkyl amine oxides Trisubstituted amine oxides and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Morpholine - Trialkyl amine oxide - N-oxide - Dialkyl ether - Ether - Trisubstituted n-oxide - Azacycle - Oxacycle - Organooxygen compound - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organopnictogen compound - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
External Descriptors	morpholine N-oxide
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	4-methyl-4-oxidomorpholin-4-ium
INCHI	InChI=1S/C5H11NO2/c1-6(7)2-4-8-5-3-6/h2-5H2,1H3
InChIKey	LFTLOKWAGJYHHR-UHFFFAOYSA-N
Smiles	C[N+]1(CCOCC1)[O-]
Isomeric SMILES	C[N+]1(CCOCC1)[O-]
WGK Germany	1
Molecular Weight	117.15
Beilstein	507437
Reaxy-Rn	507437
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=507437&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

24 results found

Lot Number	Certificate Type	Date	Item
G2301612	Certificate of Analysis	Apr 07, 2025	M105979
G2301608	Certificate of Analysis	Apr 07, 2025	M105979
G2301616	Certificate of Analysis	Apr 07, 2025	M105979
G2301613	Certificate of Analysis	Apr 07, 2025	M105979
G2301615	Certificate of Analysis	Apr 07, 2025	M105979
A2426567	Certificate of Analysis	Jan 18, 2024	M105979
A2426577	Certificate of Analysis	Jan 18, 2024	M105979
A2426570	Certificate of Analysis	Jan 18, 2024	M105979
A2426574	Certificate of Analysis	Jan 18, 2024	M105979
G2304608	Certificate of Analysis	May 17, 2023	M105979
G2301551	Certificate of Analysis	May 17, 2023	M105979
G2301553	Certificate of Analysis	May 17, 2023	M105979
G2301547	Certificate of Analysis	May 17, 2023	M105979
H2112164	Certificate of Analysis	May 11, 2023	M105979
L2215772	Certificate of Analysis	Nov 18, 2022	M105979
L2215700	Certificate of Analysis	Nov 18, 2022	M105979
L2215716	Certificate of Analysis	Nov 18, 2022	M105979
L2215816	Certificate of Analysis	Nov 18, 2022	M105979
I2216010	Certificate of Analysis	Aug 08, 2022	M105979
I2215669	Certificate of Analysis	Aug 08, 2022	M105979
I2215667	Certificate of Analysis	Aug 08, 2022	M105979
I2215668	Certificate of Analysis	Aug 08, 2022	M105979
J2019253	Certificate of Analysis	Aug 05, 2022	M105979
H1912133	Certificate of Analysis	Jun 22, 2022	M105979

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Chemical and Physical Properties

Solubility	Soluble in water, methanol, ethanol, acetone, ethers and dimethylsulfoxide.
Sensitivity	moisture sensitive
Refractive Index	1.4201
Boil Point(°C)	118.5 °C
Melt Point(°C)	180-184 °C (lit.)
Molecular Weight	117.150 g/mol
XLogP3	-0.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	117.079 Da
Monoisotopic Mass	117.079 Da
Topological Polar Surface Area	27.300 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	78.500
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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