2-Methoxyethylamine supplier

Name
2-METHOXYETHYLAMINE
EINECS 203-712-1
CAS No. 109-85-3
Article Data68
CAS DataBase
Density 0.853 g/cm³
Solubility Completely miscible in water
Melting Point -82 °C
Formula C₃H₉NO
Boiling Point 94.999 °C at 760 mmHg
Molecular Weight 75.1106
Flash Point 9.444 °C
Transport Information
Appearance clear colorless liquid
Safety 16-26-36/37/39-45
Risk Codes 11-34
Molecular Structure
Hazard Symbols F,C
Synonyms Ethylamine,2-methoxy- (6CI,7CI,8CI);1-Amino-2-methoxyethane;1-Methoxy-2-aminoethane;2-(Methyloxy)ethanamine;2-Aminoethyl methyl ether;2-Methoxy-1-aminoethane;2-Methoxy-1-ethanamine;2-Methoxyethanamine;2-Methoxyethylamine;N-(2-Methoxyethyl)amine;b-Methoxyethylamine;
PSA 35.25000
LogP 0.29180

Synthetic route

: 1119-13-7
N,N'-Di(2-methoxyethyl)thioharnstoff

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With dipotassium peroxodisulfate In water; acetonitrile at 80℃; for 6h; Temperature; Reagent/catalyst; Solvent;	83.5%

: 54149-18-7
2-(2-Methoxy-ethoxy)-isoindole-1,3-dione

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With methylhydrazine In dichloromethane at -10℃; for 2h;	77%

: 18600-40-3
(2-methoxyethyl)amine hydrochloride

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With sodium hydroxide In dichloromethane at 20 - 25℃; for 1h;	53.6%

: 107-21-1
ethylene glycol

A: 110-91-8
morpholine

B: 109-02-4
4-methyl-morpholine

C: 100-74-3
N-ethylmorpholine;

D: 109-86-4
2-methoxy-ethanol

E: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With ammonia; hydrogen at 200℃; for 0.00175h; Product distribution; 190 - 260 deg C;	A 46% B 2.1 % Chromat. C 1.4 % Chromat. D 0.7 % Chromat. E 0.6 % Chromat.

...Expand

: 67-56-1
methanol

: 861555-02-4
(2-amino-ethyl)-nitroso-amidosulfuric acid

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
reagiert analog mit Alkohol und Propylalkohol;

: 41081-97-4
2-(2-methoxyethyl)isoindoline-1,3-dione

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With sodium hydroxide
With potassium hydroxide In water

: 35461-44-0
1-methoxy-2-nitroethane

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With ethanol; platinum at 20℃; under 73550.8 Torr; Hydrogenation;

: 109-86-4
2-methoxy-ethanol

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With aluminum oxide; ammonia at 200 - 250℃;
With ammonia; nickel at 200 - 250℃;
With ammonia; hydrogen at 250℃; under 3750.38 Torr; for 2h; Reagent/catalyst;

: 1738-36-9
2-methoxyacetonitrile

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With nickel Hydrogenation;

: 23920-12-9
N-(2-methoxy-ethyl)-2,4-dinitro-aniline

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With sodium hydroxide

: 22483-14-3
(2-Methoxy-ethyl)-[2-methyl-prop-(Z)-ylidene]-amine

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
In water; benzonitrile Equilibrium constant;

: 3-Hydroxy-2-[(2-methoxy-ethylamino)-phenyl-methyl]-inden-1-one

A: 109-85-3
2-methoxyethylamine

B: 5381-33-9
2-benzylidene-indan-1,3-dione

Conditions

Conditions	Yield
With potassium chloride In water; dimethyl sulfoxide at 20℃; Rate constant; Equilibrium constant;

: C13H16NO3(1-)*H(1+)

A: 82700-43-4
benzylidenemalonaldehyde

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
In water; N,N-dimethyl-formamide at 20℃; Equilibrium constant; Rate constant;

: (2-methoxyethyl)ammonium ion

: C22H15N6O12(1-)

A: 144432-14-4
tris(5-methyl-2,4-dinitrophenyl)methane

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
In water; dimethyl sulfoxide at 25℃; Rate constant;

...Expand

: (2-methoxyethyl)ammonium ion

: C25H21N6O12(1-)

A: 144432-15-5
tris(3,5-dimethyl-2,4-dinitrophenyl)methane

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
In water; dimethyl sulfoxide at 25℃; Rate constant;

...Expand

: 80894-21-9
1-azido-2-methoxy-ethane

: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With triphenylphosphine 1.) THF, RT, 12 h, 2.) hydrolysis, RT, 12 h; Multistep reaction;

: 74158-00-2
(1S,2R,4R,6S)-6-Hydroxy-bicyclo[2.2.1]heptane-2-carboxylic acid (2-methoxy-ethyl)-amide

: 6712-12-5
endo-6-hydroxybicyclo<2.2.1>heptane-endo-2-carboxylic acid lactone

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
In methanol; water at 30℃; Rate constant;

: 141-43-5
ethanolamine

: 77-78-1
dimethyl sulfate

A: 38256-93-8
N-methyl-N-(2-methoxyethyl)amine

B: 3030-44-2
N,N-dimethyl-2-methoxyethylamine

C: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With sodium hydride 1.) THF, room temp., 1 h; 2.) room temp., 1 h; Yield given. Multistep reaction;

...Expand

: (2-Methoxy-ethyl)-thiocarbamic acid; compound with triethyl-amine

A: 463-58-1
carbon oxide sulfide

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With phosphate buffer In water at 25℃; Mechanism; Rate constant; general acid catalysis;

: 93549-60-1
N-(o-methoxybenzylidene)-2-methoxyethylamine

A: 135-02-4
ortho-anisaldehyde

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With potassium chloride; 2-methoxyethylamine In water at 30℃; Rate constant; other amines, var. pH;

: 93630-42-3
(1R,2S,3R,4S)-3-(2-Methoxy-ethylcarbamoyl)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

A: 109-85-3
2-methoxyethylamine

B: 129-64-6
3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride

Conditions

Conditions	Yield
With water at 38℃; Rate constant;

: (1R,7S)-5-Hydroxy-5-(2-methoxy-ethylamino)-4-oxa-tricyclo[5.2.1.02,6]dec-8-en-3-one

A: 109-85-3
2-methoxyethylamine

B: 129-64-6
3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride

Conditions

Conditions	Yield
With water at 38℃; Rate constant;

: 97732-02-0
C5H13NOS*ClH

A: 75-18-3
dimethylsulfide

B: 109-85-3
2-methoxyethylamine

Conditions

Conditions	Yield
With iodide; hydrogen cation In water at 25℃; Rate constant; pH dependence (pH = 0.5-3.0), μ = 1.0 with KCl;

: 107-13-1
acrylonitrile

: 109-85-3
2-methoxyethylamine

: 449165-43-9
N,N-bis(2-cyanoethyl)-2-methoxyethylamine

Conditions

Conditions	Yield
In methanol for 48h; Heating;	100%

: 1247-71-8
3,16α-diacetoxy-1,3,5(10)-estratrien-17-one

: 109-85-3
2-methoxyethylamine

: 137437-73-1
17-(2-methoxyethylimino)estra-1,3,5(10)-triene-3,16α-diol

Conditions

Conditions	Yield
for 3h; Ambient temperature;	100%

: 4530-20-5
BOC-glycine

: 118-92-3
anthranilic acid

: 109-85-3
2-methoxyethylamine

: 2-aminomethyl-3-(2-methoxyethyl)-3H-quinazolin-4-one

Conditions

Conditions	Yield
Stage #1: BOC-glycine; anthranilic acid With pyridine; triphenyl phosphite at 150℃; for 0.166667h; microwave irradiation; Stage #2: 2-methoxyethylamine at 220℃; for 0.0666667h; microwave irradiation;	100%

...Expand

: 4530-20-5
BOC-glycine

: 118-92-3
anthranilic acid

: 109-85-3
2-methoxyethylamine

: [3-(2-methoxyethyl)-4-oxo-3,4-dihydroquinazolin-2-yl-methyl]carbamic acid tert-butyl ester

Conditions

Conditions	Yield
Stage #1: BOC-glycine; anthranilic acid With pyridine; triphenyl phosphite at 150℃; for 0.166667h; microwave irradiation; Stage #2: 2-methoxyethylamine at 180℃; for 0.05h; microwave irradiation;	100%

...Expand

: 959432-07-6
5-Bromo-3-[6-chloro-2-(2-methoxy-ethyl)-2H-pyrazolo[3,4-d]pyrimidin-4-yl]-1,3-dihydro-indol-2-one

: 109-85-3
2-methoxyethylamine

: 5-Bromo-3-[2-(2-methoxy-ethyl)-6-(2-methoxy-ethylamino)-2H-pyrazolo[3,4-d]pyrimidin-4-yl]-1,3-dihydro-indol-2-one

Conditions

Conditions	Yield
	100%

: 383-63-1
ethyl trifluoroacetate,

: 109-85-3
2-methoxyethylamine

: 166252-93-3
N-(2-methoxyethyl)trifluoroacetamide

Conditions

Conditions	Yield
In diethyl ether for 24h; cooling;	100%

: 98-61-3
4-iodobenzenesulfonyl chloride

: 109-85-3
2-methoxyethylamine

: 403792-77-8
4-iodo-N-[2-(methyloxy)ethyl]benzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 1h;	100%
With triethylamine In dichloromethane at 0 - 20℃; for 1h;	100%

: 599202-33-2
2-(3-nitro-4-fluorophenyl)-5-phenylbenzoxazole

: 109-85-3
2-methoxyethylamine

: 599202-40-1
2-[3-nitro-4-(2-methoxyethylamino)phenyl]-5-phenylbenzoxazole

Conditions

Conditions	Yield
at 20℃; for 0.25h;	100%

: 78238-12-7
3-methoxy-5-nitrobenzoic acid

: 109-85-3
2-methoxyethylamine

: 1050514-17-4
3-methoxy-N-(2-methoxyethyl)-5-nitrobenzamide

Conditions

Conditions	Yield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h;	100%

: 943617-67-2
4-(4-chloro-2-nitrophenoxy)benzoyl chloride

: 109-85-3
2-methoxyethylamine

: 943617-69-4
4-(4-chloro-2-nitrophenoxy)-N-(2-methoxyethyl)benzamide

Conditions

Conditions	Yield
In 1,2-dichloro-ethane for 12h;	100%

: 1020267-12-2
10-(8'-isothiocyanato-3',6'-dioxaoct-1'-yl)-7,8-dimethylbenzo[g]pteridine-2,4-dione

: 109-85-3
2-methoxyethylamine

: 1020267-21-3
10-(9',11'-diaza-3',6',14'-trioxa-10'-thioxopentadec-1'-yl)-7,8-dimethylbenzo[g]pteridine-2,4-dione

Conditions

Conditions	Yield
With triethylamine In chloroform for 2.5h; Reflux;	100%

: 1127329-22-9
2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazole-5-carbaldehyde

: 109-85-3
2-methoxyethylamine

: 1127329-23-0
N-((2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl)-2-methoxyethanamine

Conditions

Conditions	Yield
Stage #1: 2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazole-5-carbaldehyde; 2-methoxyethylamine With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 20℃; for 24h; Stage #2: With water; sodium hydrogencarbonate In dichloromethane	100%
Stage #1: 2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazole-5-carbaldehyde; 2-methoxyethylamine With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 20℃; for 24h; Stage #2: With sodium hydrogencarbonate In dichloromethane; water

: 1203572-07-9
C7H6ClN3O4

: 109-85-3
2-methoxyethylamine

: 1203572-11-5
C10H14N4O5

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane	100%

: 98-03-3
thiophene-2-carbaldehyde

: 109-85-3
2-methoxyethylamine

: 105387-30-2
2-methoxy-N-(thiophen-2-ylmethylene)ethanamine

Conditions

Conditions	Yield
at 60℃; for 6h; Inert atmosphere;	100%
With acetic acid In methanol at 25℃; for 4h;

: 869957-51-7
di(2,4,6-tri-O-acetyl-3-deoxy-3-(4-(methoxycarbonyl)-1H-1,2,3-triazol-1-yl)-β-D-galactopyranosyl)sulfane

: 109-85-3
2-methoxyethylamine

: 1242965-45-2
di(3-deoxy-3-(4-((2-methoxyethylamino)carbonyl)-1H-1,2,3-triazol-1-yl)-β-D-galactopyranosyl)sulfane

Conditions

Conditions	Yield
With methanol for 28h;	100%

: 1493-27-2
ortho-nitrofluorobenzene

: 109-85-3
2-methoxyethylamine

: 56436-24-9
[2-(methyloxy)ethyl](2-nitrophenyl)amine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In ethanol at 150℃; for 0.316667h; Sealed vial;	100%
In ethanol at 20℃;
In N,N-dimethyl-formamide at 20℃;
In dichloromethane at 20℃; for 8h; Inert atmosphere;
In dichloromethane for 6h; Inert atmosphere;

: 1307314-58-4
2-[4-[(2-chloro-4,4-difluoro-spiro[5H-thieno[2,3-c]pyran-7,4'-piperidine]-1'-yl)methyl]-3-methyl-pyrazol-1-yl]-3-fluoro-benzaldehyde

: 109-85-3
2-methoxyethylamine

: 1307314-59-5
N-(2-(4-((2'-chloro-4',4'-difluoro-4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran]-1-yl)methyl)-3-methyl-1H-pyrazol-1-yl)-3-fluorobenzylidene)-2-methoxyethanamine

Conditions

Conditions	Yield
In dichloromethane Molecular sieve;	100%

: 1232365-39-7
2-(1-((tert-butoxycarbonyl)amino)cyclobutyl)-2-hydroxyacetic acid

: 109-85-3
2-methoxyethylamine

: 1311198-98-7
tert-butyl 1-(1-hydroxy-2-(2-methoxyethylamino)-2-oxoethyl)cyclobutylcarbamate

Conditions

Conditions	Yield
Stage #1: 2-(1-((tert-butoxycarbonyl)amino)cyclobutyl)-2-hydroxyacetic acid; 2-methoxyethylamine With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 0.166667h; Cooling with ice; Stage #2: With HATU In N,N-dimethyl-formamide for 1h;	100%

: 13091-23-1
4-chloro-3-nitropyridine

: 109-85-3
2-methoxyethylamine

: 1040063-55-5
N-[2-(methyloxy)ethyl]-3-nitro-4-pyridinamine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In ethanol at 150℃; for 0.316667h; Microwave vial;	100%

: 109-85-3
2-methoxyethylamine

: 4-fluoro-N-(2-morpholin-4-yl-ethyl)-3-nitro-benzamide

: 1015992-68-3
4-{[2-(methyloxy)ethyl]amino}-N-[2-(4-morpholinyl)ethyl]-3-nitrobenzamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In ethanol at 150℃; for 0.0833333h; Microwave irradiation;	100%

: 14002-80-3
Methyl 2,2-dimethyl-3-hydroxypropionate

: 109-85-3
2-methoxyethylamine

: 1093206-21-3
3-hydroxy-N-(2-methoxyethyl)-2,2-dimethylpropanamide

Conditions

Conditions	Yield
	100%

: 24623-61-8
3,5-dimethylsalicylaldehyde

: 109-85-3
2-methoxyethylamine

: 1395897-97-8
C12H17NO2

Conditions

Conditions	Yield
In methanol for 12h; Reflux;	100%
In methanol Reflux;	95%

: 109-85-3
2-methoxyethylamine

: 90-60-8
3,5-dichlorosalicyclaldehyde

: 1613543-67-1
C10H11Cl2NO2

Conditions

Conditions	Yield
In methanol for 12h; Reflux;	100%

: 90-59-5
3,5-Dibromosalicylaldehyde

: 109-85-3
2-methoxyethylamine

: 847753-50-8
C10H11Br2NO2

Conditions

Conditions	Yield
In methanol for 12h; Reflux;	100%

: 24623-65-2
3-tert-butyl-2-hydroxybenzaldehyde

: 109-85-3
2-methoxyethylamine

: 1613543-72-8
C14H21NO2

Conditions

Conditions	Yield
In methanol for 12h; Reflux;	100%

: C14H13N3O3

: 109-85-3
2-methoxyethylamine

: C17H20N4O3

Conditions

Conditions	Yield
Stage #1: C14H13N3O3 With triethylamine In acetonitrile at 20℃; for 0.0833333h; Stage #2: With bis(pentafluorophenyl)carbonate In acetonitrile at 20℃; for 0.75h; Stage #3: 2-methoxyethylamine With triethylamine In acetonitrile at 20℃; for 18h;	100%

: 7-phenylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid

: 109-85-3
2-methoxyethylamine

: N-(2-methoxyethyl)-7-phenylpyrazolo[1,5-a]pyrimidine-3-carboxamide

Conditions

Conditions	Yield
Stage #1: 7-phenylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid With triethylamine In N,N-dimethyl-formamide at 20℃; for 0.0833333h; Stage #2: With bis(pentafluorophenyl)carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Stage #3: 2-methoxyethylamine With triethylamine In N,N-dimethyl-formamide at 20℃; for 24h;	100%

: 364-73-8
4-Bromo-1-fluoro-2-nitrobenzene

: 109-85-3
2-methoxyethylamine

: (4-bromo-2-nitrophenyl)-(2-methoxyethyl)amine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 85℃; for 16h; Inert atmosphere;	100%
In ethanol at 20℃; for 24h;	67%

: methanesulfonic acid 2-{4-[(4-benzyloxy-phenyl)-methyl-amino]-phenyl}-propyl ester

: 109-85-3
2-methoxyethylamine

: (4-{2-[(2-methoxyethyl)amino]-isopropyl}phenyl)methyl [4(phenylmethoxy)phenyl]amine

Conditions

Conditions	Yield
With sodium hydrogencarbonate In acetonitrile at 70℃;	100%

: 4-(4-(((tert-butoxycarbonyl)amino)methyl)pyridin-2-yl)benzoic acid

: 109-85-3
2-methoxyethylamine

: tert-butyl ((2-(4-((2-methoxyethyl)carbamoyl)phenyl)pyridin-4-yl)methyl)

Conditions

Conditions	Yield
Stage #1: 4-(4-(((tert-butoxycarbonyl)amino)methyl)pyridin-2-yl)benzoic acid With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; for 0.166667h; Stage #2: 2-methoxyethylamine With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 20h;	100%

2-Methoxyethylamine Chemical Properties

Chemistry informtion about 2-Methoxyethylamine (CAS NO.109-85-3) is:
IUPAC Name: 2-Methoxyethanamine
Synonyms: 2-Aminoethyl Methyl Ether ; 2-Methoxyethylamine ; Rarechem Al Bw 0200 ; O-Methylethanolamine ; 1-Methoxy-2-Aminoethane ; 2-Methoxy-Ethanamin ; 2-Methoxyethanamine ; 2-Methoxy-Ethylamin
MF: C₃H₉NO
MW: 75.11
EINECS: 203-712-1
Density: 0.852 g/cm³
Melting Point: -82 °C
Flash Point: 9.4 °C
Boiling Point: 95 °C at 760 mmHg
Vapour Pressure: 46.3 mmHg at 25°C
Enthalpy of Vaporization: 33.47 kJ/mol
Refractive Index: n20/D 1.406(lit.)
Storage temp.: Flammables area
BRN: 741854
Following is the molecular structure of 2-Methoxyethylamine (CAS NO.109-85-3) is:

2-Methoxyethylamine Uses

2-Methoxyethylamine (CAS NO.109-85-3) was used for synthetic intermediates.

2-Methoxyethylamine Production

Preparation Products is Bis(2-Methoxyethyl)Amine .

2-Methoxyethylamine Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LD50	intraperitoneal	400mg/kg (400mg/kg)		National Technical Information Service. Vol. AD691-490,
mouse	LDLo	oral	1600mg/kg (1600mg/kg)	behavioral: tremor behavioral: muscle weakness behavioral: ataxia	National Technical Information Service. Vol. OTS0546426,
rat	LDLo	oral	1600mg/kg (1600mg/kg)	behavioral: muscle weakness lungs, thorax, or respiration: dyspnea lungs, thorax, or respiration: cyanosis	National Technical Information Service. Vol. OTS0546426,

2-Methoxyethylamine Consensus Reports

Reported in EPA TSCA Inventory.

2-Methoxyethylamine Safety Profile

Poison by intraperitoneal route. When heated to decomposition it emits toxic fumes of NO_x. See also AMINES.
Hazard Codes:
F
Corrosive C
Risk Statements:
R11:Highly flammable.
R34:Causes burns.
Safety Statements:
S16:Keep away from sources of ignition.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: UN 2733 3/PG 2
WGK Germany: 3
RTECS: KR8750000
HazardClass: 3
PackingGroup: II

2-Methoxyethylamine Analytical Methods

By glycol monomethyl ether and ammonia in the nickel or alumina catalysts under high-temperature dehydration in, or methicillin-acetonitrile nickel to be catalytic hydrogenation.

2-Methoxyethylamine Specification

2-Methoxyethylamine (CAS NO.109-85-3) is a clear colorles liquid. It combustible and can soluble in ethanol and ether.

Product Name

2-METHOXYETHYLAMINE

Synthetic route

2-Methoxyethylamine Chemical Properties

2-Methoxyethylamine Uses

2-Methoxyethylamine Production

2-Methoxyethylamine Toxicity Data With Reference

2-Methoxyethylamine Consensus Reports

2-Methoxyethylamine Safety Profile

2-Methoxyethylamine Analytical Methods

2-Methoxyethylamine Specification

Related Products

Hot Products