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109-02-4

  • Product Name:4-Methylmorpholine
  • Molecular Formula:C5H11NO
  • Molecular Weight:101.148
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Product Details

Detail

  • Cas No: 109-02-4
  • Molecular Formula: C5H11NO
  • Appearance: clear liquid
  • Purity: 99%
Product Name N-Methylmorpholine
Alias 1-Methylmorpholine ;4-Methylmorpholine;Morpholine,N-methyl
English
Molecular formula

C5H11NO

Molecular weight 101.15
CAS No 109-02-4
EINECS
Specification

Assay(GC)99%    

Water :<0.3%;

Color :<100#(APHA)

Appearance traits Colorless liquid, with the smell of ammonia
Use Medium of pharmaceuticals and chemical synthesis of organic synthetic raw material, the analytical reagent, extraction solvent, chlorine hydrocarbon stabilizer, corrosion inhibitor and dispersant, catalyst, medicine production, etc
Package 180kg/drum
Other product information

Properties: 

Melting point:−66°C(lit.)

Boiling point:115-116°C750 mm hg(lit.)

Density:0.92 g/ml at 25°C(lit.)

Vapor density:>1 (vs air)

Vapour pressure:18 mm hg ( 20°C)

Refractive index:N20/D 1.435(lit.)

Flash(ing) point:75 °F

Water soluble properties:>500 g/L (20ºc)

Factory supply  4-Methylmorpholine 109-02-4 (N-Methyl morphofine)  with low price

  • Molecular Formula:C5H11NO
  • Molecular Weight:101.148
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:18 mm Hg ( 20 °C) 
  • Melting Point:-66 °C(lit.) 
  • Refractive Index:n20/D 1.435(lit.)  
  • Boiling Point:114.1 °C at 760 mmHg 
  • PKA:7.38(at 25℃) 
  • Flash Point:23.9 °C 
  • PSA:12.47000 
  • Density:0.931 g/cm3 
  • LogP:-0.11370 

4-Methylmorpholine(Cas 109-02-4) Usage

Preparation

4-Methylmorpholine preparation method is to slowly add formaldehyde in morpholine drop by drop, under stirring add formic acid reaction, automatic reflux, and release carbon dioxide. After adding formic acid, heating reflux 4 ~ 5h, cooling and adding sodium hydroxide immediately distillation, collect all the fraction before the boiling point of 99 ℃, and then add sodium hydroxide in the fraction to saturation, cooling the oil layer, drying, fractional distillation, to obtain N-methylmorpholine.

Synthesis Reference(s)

Tetrahedron Letters, 36, p. 4881, 1995 DOI: 10.1016/0040-4039(95)00875-D

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Hazard

Flammable, dangerous fire risk. Skin irri-tant.

Health Hazard

May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Flammable

Safety Profile

Moderately toxic by ingestion and skin contact. Mildly toxic by inhalation. An irritant to skin, eyes, and mucous membranes. Flammable when exposed to heat or flame, can react vigorously with oxidizing materials. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Dry it by refluxing with BaO or sodium, then fractionally distil it through a helices-packed column. The picrate has m 227o, the thiocyanate salt has m 103o (from butanone). [Hall J Phys Chem 60 63 1956, Beilstein 27 I 203, 27 III/IV 22.]

General Description

A water-white liquid with an ammonia-like odor. Less dense than water and insoluble in water. Flash point 75°F. May be moderately toxic by ingestion, inhalation and skin absorption. Very irritating to skin, eyes, and mucous membranes. Used as a solvent and to make pharmaceuticals.

InChI:InChI=1/C5H11NO/c1-6-2-4-7-5-3-6/h2-5H2,1H3/p+1

Our main markets are China, the United States, Europe, Korea, and Japan. The main business scope includes electronic chemicals, liquid crystal intermediates, high-purity metal compounds, pharmaceutical intermediates, special chemicals, and so on.

109-02-4 Relevant articles

Waste-free technology for N-methylmorpholine synthesis

Markosyan,Baghdasaryan,Hovhannisyan,Attaryan,Hasratyan

, (2013)

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Synthesis of N-methylmorpholine from morpholine and dimethyl carbonate

Zhu, Maodian,Liu, Shaoying,Deng, Zhiyong,Wang, Gongying

, p. 8427 - 8430 (2013)

The synthesis of N-methylmorpholine from...

Glycerol as a Building Block for Prochiral Aminoketone, N-Formamide, and N-Methyl Amine Synthesis

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, p. 3133 - 3138 (2016)

Prochiral aminoketones are key intermedi...

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, p. 15403 - 15411 (2020)

The first acceptor-free heavier germaniu...

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Sarf et al.

, (1968)

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On the chemical interactions of the biomass processing agents γ-valerolactone (GVL) and: N -methylmorpholine- N -oxide (NMMO)

Bacher, Markus,Hettegger, Hubert,Jusner, Paul,Lê, Huy Quang,Potthast, Antje,Rosenau, Thomas,Sixta, Herbert

, p. 5832 - 5848 (2021)

In new biorefinery processes, NMMO/water...

Radicals derived from N-methylmorpholine-N-oxide (NMMO): Structure, trapping and recombination reactions

Rosenau,Potthast,Sixta,Kosma

, p. 3073 - 3078 (2002)

The two carbon-centered radicals 4-morph...

Chiral phosphorus(III) triflates. On the nature of the phosphorus-oxygen interaction

Jones, Victoria A.,Sriprang, Sarin,Thornton-Pett, Mark,Kee, Terence P.

, p. 199 - 218 (1998)

Reaction of chiral phosphorodiamidites w...

Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO2/H2 catalyzed by an ionic liquid-Pd/C system

Li, Ruipeng,Zhao, Yanfei,Wang, Huan,Xiang, Junfeng,Wu, Yunyan,Yu, Bo,Han, Buxing,Liu, Zhimin

, p. 9822 - 9828 (2019)

The reduction of CO2 with amines and H2 ...

An Improved Rapid and Mild Deoxygenation of Amine N-oxides

Rajesh

, p. 486 - 491 (2018)

An improved mild and selective method fo...

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Kim et al.

, p. 198 (1971)

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Self-Sufficient Formaldehyde-to-Methanol Conversion by Organometallic Formaldehyde Dismutase Mimic

van der Waals, Dominic,Heim, Leo E.,Vallazza, Simona,Gedig, Christian,Deska, Jan,Prechtl, Martin H. G.

, p. 11568 - 11573 (2016)

The catalytic networks of methylotrophic...

Germyliumylidene: A Versatile Low Valent Group 14 Catalyst

Sarkar, Debotra,Dutta, Sayan,Weetman, Catherine,Schubert, Emeric,Koley, Debasis,Inoue, Shigeyoshi

, p. 13072 - 13078 (2021)

Bis-NHC stabilized germyliumylidenes [RG...

Chemoselective deoxygenation of nitrones and N-oxides with tetrathiomolybdate

Ilankumaran, Palanichamy

, p. 4881 - 4882 (1995)

Reaction of nitrones and N-oxides with b...

Kinetic evidence for the formation of monocationic N,N′-disubstituted phthalamide in tertiary amine-catalyzed hydrolysis of N-substituted phthalimides

Sim, Yoke-Leng,Ariffin, Aznar,Khan, M. Niyaz

, p. 8452 - 8458 (2007)

(Chemical Equation Presented) A kinetic ...

Additive-free selective methylation of secondary amines with formic acid over a Pd/In2O3 catalyst

Benaissa, Idir,Cantat, Thibault,Genre, Caroline,Godou, Timothé,Pinault, Mathieu

, p. 57 - 61 (2022/01/19)

Formic acid is used as the sole carbon a...

Reactivity of heterocyclic α-aminomethylsilanes with alcohols

Pypowski, Krzysztof,Mojzych, Mariusz

, p. 320 - 324 (2021/03/31)

[Figure not available: see fulltext.] Al...

Electrochemical Activation of Diverse Conventional Photoredox Catalysts Induces Potent Photoreductant Activity**

Chernowsky, Colleen P.,Chmiel, Alyah F.,Wickens, Zachary K.

supporting information, p. 21418 - 21425 (2021/08/25)

Herein, we disclose that electrochemical...

Borane-Trimethylamine Complex as a Reducing Agent for Selective Methylation and Formylation of Amines with CO2

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supporting information, p. 8282 - 8286 (2021/10/25)

We report herein that a borane-trimethyl...

109-02-4 Process route

C<sub>19</sub>H<sub>22</sub><sup>(2)</sup>H<sub>2</sub>NO<sup>(1+)</sup>

C19H22(2)H2NO(1+)

4-methyl-morpholine
109-02-4

4-methyl-morpholine

trans-1,2-dideuteriostilbene
5284-44-6

trans-1,2-dideuteriostilbene

Conditions
Conditions Yield
With N,N'-bis-(4-ethoxy-phenyl)-thiourea; In ethanol; at 40 ℃; Rate constant;
 
4-methyl-4-(morpholinomethyl)morpholinium sulfate

4-methyl-4-(morpholinomethyl)morpholinium sulfate

morpholine
110-91-8,99108-56-2

morpholine

4-methyl-morpholine
109-02-4

4-methyl-morpholine

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

Conditions
Conditions Yield
In water; Product distribution;
 

109-02-4 Upstream products

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    110-91-8

    morpholine

  • 67-56-1
    67-56-1

    methanol

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    formaldehyd

  • 80-48-8
    80-48-8

    methyl p-toluene sulfonate

109-02-4 Downstream products

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    6-[2,2-bis-(4-chloro-phenyl)-acetylamino]-benzo[1,3]dioxole-5-carboxylic acid methyl ester

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