N-Ethylmethylamine supplier

Name
N-Ethylmethylamine
EINECS 210-862-1
CAS No. 624-78-2
Article Data60
CAS DataBase
Density 0.68 g/cm³
Solubility
Melting Point -70.99°C (estimate)
Formula C₃H₉N
Boiling Point 36.7 °C at 760 mmHg
Molecular Weight 59.1112
Flash Point <?30°F
Transport Information UN 2733 3/PG 1
Appearance clear colorless to light yellow liquid
Safety 26-36/37/39-45
Risk Codes 11-20/21/22-35
Molecular Structure
Hazard Symbols F; C
Synonyms N-methyl-aminoethane;Methylaminoethane;2-MAE;N-METHYLETHYLAMINE;Methylethylamine;n-methyl-ethanamin;(CH3)(C2H5)NH;Ethylmethylamine;methyl-N-ethylamine;N-ethyl-N-methylamine;
PSA 12.03000
LogP 0.61660

Synthetic route

: 75-07-0
acetaldehyde

: 74-89-5
methylamine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With hydrogen; sodium hydroxide; Raney nickel at 65 - 67℃; under 22502.3 Torr; for 4.3h; Product distribution / selectivity; Autoclave; Industry scale;	90%
With potassium hydroxide; dipotassium hydrogenphosphate; phosphoric acid at 10 - 12℃; for 4h; electrochemical reductive amination, lead cathode, current density 0.05 A/cm2, pH 12; Yield given;
With imine reductase from Streptomyces ipomoeae; NADPH In water at 30℃; for 0.166667h; pH=9.5; Catalytic behavior; Reagent/catalyst; Enzymatic reaction;

: 6898-67-5
N-ethylidenemethylamine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With hydrogen; platinum(IV) oxide In ethanol	80%

: 3710-84-7
N-ethyl-N-hydroxy-ethanamine

A: 50-00-0
formaldehyd

B: 624-78-2
N-Ethylmethylamine

C: 75-04-7
ethylamine

D: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With phosphorus pentachloride In toluene at 18 - 20℃; Mechanism; Product distribution; object of study: Stieglitz rearrangement (prototype);	A n/a B 1.4% C 76% D n/a

...Expand

: 6852-54-6
N-(benzylidene)ethylamine

: 5187-82-6
(ethoxycarbonylmethyl)dimethylsulfonium bromide

A: 624-78-2
N-Ethylmethylamine

B: 94117-87-0
1-methylthio-3-phenyl-1,2-cyclopropanedicarboxylic acid diethyl ester

Conditions

Conditions	Yield
With potassium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In tetrahydrofuran at 20℃; for 4h;	A n/a B 50%

...Expand

: 110-86-1
pyridine

: 616-39-7
N,N-diethylnmethylamine

: 94-36-0
dibenzoyl peroxide

A: 50-00-0
formaldehyd

B: 624-78-2
N-Ethylmethylamine

C: 75-07-0
acetaldehyde

D: 109-89-7
diethylamine

...Expand

: 60-29-7
diethyl ether

: 6154-14-9
N-chloromethylamine

: 557-20-0
diethylzinc

A: 624-78-2
N-Ethylmethylamine

B: 74-89-5
methylamine

...Expand

: 7651-91-4
N,N-dichloromethylamine

: 557-20-0
diethylzinc

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With Petroleum ether

: 10595-95-6
N-nitrosomethylethylamine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With hydrogenchloride

: 4788-37-8
N-ethyl-N-methylbenzylamine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With platinum(IV) oxide; acetic acid at 65 - 75℃; under 2206.5 Torr; durch Hydrogenolyse;

: 75-04-7
ethylamine

: 74-88-4
methyl iodide

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With ethanol at 100℃;

: 4186-68-9
1-Ethyl-1-methylpyrrolidinium iodide

: 141-43-5
ethanolamine

A: 120-94-5
1-Methylpyrrolidine

B: 7335-06-0
1-ethylpyrrolidine

C: 2955-88-6
1-pyrrolidineethanol

D: 624-78-2
N-Ethylmethylamine

...Expand

: 109-90-0
ethyl isocyanate

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; 3,6,9-trioxaundecane
With hydrogen; nickel at 180 - 190℃;

: 108-24-7
acetic anhydride

: 596-58-7, 70630-96-5, 70630-97-6, 70680-98-7
(RS)-disinomenine

A: 624-78-2
N-Ethylmethylamine

B: 3.7.3'.7'-Tetramethoxy-4.6.4'.6'-tetraacetoxy-diphenanthryl-(1.1')

Conditions

Conditions	Yield
at 180℃; isomer(ic) I;

...Expand

: 57-27-2
MORPHIN

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With potassium hydroxide at 180℃;

: 27126-11-0
N-Diphenylmethylen(ethyl)amin

: 74-88-4
methyl iodide

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
Kochen des endstandenen Jodmethylats mit Alkohol;

: 74-83-9
methyl bromide

: 1946-09-4
diethyl N-ethylphosphoramidate

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
(i) aq. NaOH, HSO4, (ii) HCl; Multistep reaction;

: 6852-54-6
N-(benzylidene)ethylamine

: 77-78-1
dimethyl sulfate

: 624-78-2
N-Ethylmethylamine

: 74-96-4
ethyl bromide

: 74-89-5
methylamine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
In ethanol at 100℃; under 3677.5 Torr;

: 7779-27-3
1,3,5-triethyl-1,3,5-triazacyclohexane

: 91076-68-5
mono-trimethylsilylphosphite

A: 598-56-1
N,N-dimethyl-ethanamine

B: 624-78-2
N-Ethylmethylamine

...Expand

: 38806-26-7
N-Ethyl,N-methylacetamide

A: 624-78-2
N-Ethylmethylamine

B: 71-50-1
acetate

Conditions

Conditions	Yield
With sodium hydroxide In water at 100℃; Rate constant; Mechanism;

: 519-73-3
triphenylmethane

: 57018-31-2
lithium ethylmethyl amide

A: 624-78-2
N-Ethylmethylamine

B: 733-90-4
trityllithium

Conditions

Conditions	Yield
In tetrahydrofuran at 30℃; Equilibrium constant;

...Expand

: N-Methyl-N-ethylamino-triphenyl-phosphonium-jodid

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With water; hydroxide

: 51-75-2
nitrogen mustard

A: 64-17-5
ethanol

B: 624-78-2
N-Ethylmethylamine

C: 616-39-7
N,N-diethylnmethylamine

Conditions

Conditions	Yield
With potassium hydroxide; aluminum nickel In methanol Product distribution; degradation under various conditions with preparation of nonmutagenic reaction mixtures of products;

...Expand

: 107-12-0
propiononitrile

Devarda's's alloy: Devarda's's alloy

A: 624-78-2
N-Ethylmethylamine

B: 627-35-0
methyl-n-propylamine

C: 75-04-7
ethylamine

D: 123-38-6
propionaldehyde

Conditions

Conditions	Yield
weiteres Produkt:Ammoniak;

...Expand

: 107-12-0
propiononitrile

magnesium copper: magnesium copper

A: 624-78-2
N-Ethylmethylamine

B: 627-35-0
methyl-n-propylamine

C: 75-04-7
ethylamine

D: 123-38-6
propionaldehyde

Conditions

Conditions	Yield
weiteres Produkt:Ammoniak;

...Expand

: 109-90-0
ethyl isocyanate

hydrogen: hydrogen

nickel: nickel

A: 624-78-2
N-Ethylmethylamine

B: 7664-41-7
ammonia

C: 75-04-7
ethylamine

D: 109-89-7
diethylamine

Conditions

Conditions	Yield
at 180 - 190℃; Produkt 5: Triaethylamin;

...Expand

1.3.5-triethyl-hexahydro-1.3.5-triazine: 1.3.5-triethyl-hexahydro-1.3.5-triazine

: 624-78-2
N-Ethylmethylamine

Conditions

Conditions	Yield
With hydrogenchloride; zinc zuletzt bei Siedetemperatur;

: 624-78-2
N-Ethylmethylamine

: 91-56-5
indole-2,3-dione

: (2-Amino-phenyl)-oxo-acetic acid; compound with ethyl-methyl-amine

Conditions

Conditions	Yield
In water Heating;	100%

: 624-78-2
N-Ethylmethylamine

: 287721-05-5
4-[phenyl(endo-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)amino]benzoic acid

: 287720-97-2
N-ethyl-N-methyl-4-[(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl-amino]-benzamide

Conditions

Conditions	Yield
With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate Acylation;	100%

: C16H20N2O5S

: 624-78-2
N-Ethylmethylamine

: 954424-88-5
ethyl-methyl-{3-[3-(4-methyl-piperidin-1-yl)-4-nitro-phenyl]-prop-2-ynyl}-amine

Conditions

Conditions	Yield
In dichloromethane for 0.333333h; Heating / reflux;	100%

: 945001-04-7
3-[3-(phenylsulfonyl)-1H-indol-4-yl]propyl 4-methylbenzenesulfonate

: 624-78-2
N-Ethylmethylamine

: N-ethyl-N-methyl-3-[3-(phenylsulfonyl)-1H-indol-4-yl]propan-1-amine hydrochloride

Conditions

Conditions	Yield
Stage #1: 3-[3-(phenylsulfonyl)-1H-indol-4-yl]propyl 4-methylbenzenesulfonate; N-Ethylmethylamine In tetrahydrofuran at 65℃; for 16h; Stage #2: With sodium hydroxide; water In tetrahydrofuran	100%
Stage #1: 3-[3-(phenylsulfonyl)-1H-indol-4-yl]propyl 4-methylbenzenesulfonate; N-Ethylmethylamine In tetrahydrofuran at 65℃; for 16h; Stage #2: With hydrogenchloride In ethanol	69%

: 624-78-2
N-Ethylmethylamine

: 1263868-77-4
2,4-dichloro-8-phenyl-7,8-dihydro-5H-pyrano[4,3-d]pyrimidine

: 1263868-83-2
2-chloro-N-ethyl-N-methyl-8-phenyl-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

Conditions

Conditions	Yield
In methanol at 20℃; for 1h;	100%
In methanol at 20℃; for 1h;	100%

: 624-78-2
N-Ethylmethylamine

: 1263870-09-2
2,4-dichloro-8-(4-fluorophenyl)-5,6,7,8-tetrahydroquinazoline

: 1263870-13-8
2-chloro-N-ethyl-8-(4-fluorophenyl)-N-methyl-5,6,7,8-tetrahydroquinazolin-4-amine

Conditions

Conditions	Yield
In methanol at 20℃; for 0.5h;	100%
In methanol at 20℃; for 0.5h;	100%

: 624-78-2
N-Ethylmethylamine

: 1263868-24-1
2,4-dichloro-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine

: 1263868-27-4
2-chloro-N-ethyl-N-methyl-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine

Conditions

Conditions	Yield
In methanol at 20℃; for 1h;	100%
In methanol at 20℃; for 1h;	100%

: 624-78-2
N-Ethylmethylamine

: 29769-77-5
3-methoxy-4-methyl-3-cyclobutene-1,2-dione

: 3-(ethyl(methyl)amino)-4-methylcyclobut-3-ene-1,2-dione

Conditions

Conditions	Yield
In methanol at 20℃; for 4h;	100%

: 75-15-0
carbon disulfide

: 624-78-2
N-Ethylmethylamine

: lithium N-ethyl-N-methyldithiocarbamate

Conditions

Conditions	Yield
Stage #1: N-Ethylmethylamine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.25h; Stage #2: carbon disulfide In tetrahydrofuran; hexane at 20℃; for 3h;	100%

: 13139-16-7
N-(tert-butyloxycarbonyl)-L-isoleucine

: 624-78-2
N-Ethylmethylamine

: N-[N-(tert-butyloxycarbonyl)-L-isoleucyl]-N-ethyl-N-methylamine

Conditions

Conditions	Yield
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate In triethylamine; N,N-dimethyl-formamide Ambient temperature;	99%

: 4-(2-ethyl-3-chloropyridyl-4-oxy)-2,5-xylidine

: 624-78-2
N-Ethylmethylamine

: 149-73-5
trimethyl orthoformate

: N-ethyl-N-methyl-N'-[4-(2-ethyl-3-chloropyridyl-4-oxy)-2,5-xylyl]formamidine

Conditions

Conditions	Yield
Stage #1: 4-(2-ethyl-3-chloropyridyl-4-oxy)-2,5-xylidine; trimethyl orthoformate With toluene-4-sulfonic acid for 3h; Heating / reflux; Stage #2: N-Ethylmethylamine In dichloromethane at 20℃; for 16h;	99%

...Expand

: 624-78-2
N-Ethylmethylamine

: 1160490-11-8
methyl 2-(methylthio)benzo[d]oxazole-6-carboxylate

: 1160490-12-9
C12H14N2O3

Conditions

Conditions	Yield
In tetrahydrofuran at 70℃;	99%
In tetrahydrofuran at 70℃;

: 75-15-0
carbon disulfide

: 624-78-2
N-Ethylmethylamine

: 155722-99-9
C2H5CH3NC(S)SSC(S)NCH3C2H5

Conditions

Conditions	Yield
With oxygen In isopropyl alcohol at 50℃; under 1275.13 Torr; for 2h; Autoclave;	98.6%

: 624-78-2
N-Ethylmethylamine

: 36260-79-4
N,N-chloromethylethylamine

Conditions

Conditions	Yield
With N-chloro-succinimide under 0.004 Torr; Ambient temperature; stored at t<-20 deg C;	98%
With N-chloro-succinimide under 1E-05 Torr; Ambient temperature; Yield given;
With sodium hypochlorite; sodium perchlorate In water at 24.85℃; Kinetics; Further Variations:; Temperatures; Chlorination;

: 624-78-2
N-Ethylmethylamine

: 1711-05-3
m-anisoyl chloride

: 207558-42-7
N-ethyl-3-methoxy-N-methylbenzamide

Conditions

Conditions	Yield
In dichloromethane at 0℃; for 2h;	98%

: 624-78-2
N-Ethylmethylamine

: 942035-74-7
1-(6-bromo-3,4-dihydroquinolin-1(2H)-yl)-2-chloroethanone

: 1063408-94-5
1-(6-bromo-3,4-dihydroquinolin-1(2H)-yl)-2-(ethyl(methyl)amino)ethanone

Conditions

Conditions	Yield
With potassium iodide In tetrahydrofuran at 20 - 65℃; for 3h;	98%
With potassium iodide In tetrahydrofuran at 20 - 65℃; for 3h; Inert atmosphere;	98%

: 624-78-2
N-Ethylmethylamine

: 2816-54-8
triisopropylchlorogermane

: 1147551-48-1
ethylmethylaminotriisopropylgermane

Conditions

Conditions	Yield
Stage #1: N-Ethylmethylamine With n-butyllithium In diethyl ether at 0℃; for 2h; Cooling with ice; Stage #2: triisopropylchlorogermane In diethyl ether at 0 - 20℃;	98%

: 624-78-2
N-Ethylmethylamine

: 2004-06-0
6-Chloropurine riboside

: (2R,3R,4S,5R)-2-(6-(ethyl(methyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

Conditions

Conditions	Yield
With triethylamine In ethanol at 60℃; for 18h;	98%
With triethylamine In ethanol Reflux;	0.93 g

: 624-78-2
N-Ethylmethylamine

: 4-isocyanobenzenesulfonyl chloride

: N-ethyl-4-isocyano-N-methylbenzenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 25℃; for 1h;	98%

: 524-38-9
N-hydroxyphthalimide

: 624-78-2
N-Ethylmethylamine

: N-ethyl-2-(3-ethyl-3-methylureido)-N-methylbenzamide

Conditions

Conditions	Yield
With triethyl phosphite In toluene at 50℃; for 12h;	98%

: 3-(1-hydroxy-1-phenyl-methylene)-6-carboxy-2-indolinone

: 624-78-2
N-Ethylmethylamine

: 3-(1-hydroxy-1-phenyl-methylene)-6-(N-ethyl-methylcarbamoyl)-2-indolinone

Conditions

Conditions	Yield
With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 12h;	97%

: 945000-91-9
2-[3-(phenylsulfonyl)-1H-indol-4-yl]ethyl 4-methylbenzenesulfonate

: 624-78-2
N-Ethylmethylamine

: N-ethyl-N-methyl-N-{2-[3-(phenylsulfonyl)-1H-indol-4-yl]ethyl}amine hydrochloride

Conditions

Conditions	Yield
Stage #1: 2-[3-(phenylsulfonyl)-1H-indol-4-yl]ethyl 4-methylbenzenesulfonate; N-Ethylmethylamine In tetrahydrofuran at 71℃; for 24h; Stage #2: With ammonia In ethanol; dichloromethane Stage #3: With hydrogenchloride; water In diethyl ether	97%

: 624-78-2
N-Ethylmethylamine

: 1253768-91-0
(Z)-3-(hydroxy-phenyl-methylene)-2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid

: 1253768-93-2
(Z)-3-(hydroxy-phenyl-methylene)-2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid N-methyl-N-ethylamide

Conditions

Conditions	Yield
Stage #1: (Z)-3-(hydroxy-phenyl-methylene)-2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: N-Ethylmethylamine In N,N-dimethyl-formamide at 20℃; for 24h;	97%

: 624-78-2
N-Ethylmethylamine

: 1144520-57-9
ethyl 2-chloro-5-methyloxazole-4-carboxylate

: ethyl 2-(N-ethylmethylamino)-5-methyloxazole-4-carboxylate

Conditions

Conditions	Yield
at 20℃; for 13.5h;	97%

: 624-78-2
N-Ethylmethylamine

: ethyl 8-bromo-2-chloroimidazo[1,2-b]pyridazine-7-carboxylate

: ethyl 2-chloro-8-(ethyl(methyl)amino)imidazo[1,2-b]pyridazine-7-carboxylate

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 20℃; Inert atmosphere;	96.7%

: 624-78-2
N-Ethylmethylamine

: (R,E)-2-((4-(3,5-dimethoxystyryl)phenoxy)methyl)oxirane

: (R,E)-1-(4-(3,5-dimethoxystyryl)phenoxy)-3-(ethyl(methyl)amino)propan-2-ol

Conditions

Conditions	Yield
In methanol at 65℃; Inert atmosphere; Darkness;	96.3%

: [2-(3-isopropyl-[1,2,4]triazolo[4,3-a]pyridin-6-ylsulfanyl)-benzyl]-carbamic acid phenyl ester

: 624-78-2
N-Ethylmethylamine

: 745827-35-4
1-ethyl-3-[2-(3-isopropyl-[1,2,4]triazolo[4,3-a]pyridin-6-ylsulfanyl)-benzyl]-1-methyl-urea

Conditions

Conditions	Yield
Stage #1: [2-(3-isopropyl-[1,2,4]triazolo[4,3-a]pyridin-6-ylsulfanyl)-benzyl]-carbamic acid phenyl ester; N-Ethylmethylamine In dimethyl sulfoxide at 20℃; for 0.5h; Stage #2: In water	96%

: methyl 5-chloro-7-[(3-methylphenyl)amino]-1-[2-(2,2,2-trifluoroethoxy)ethyl]-1H-pyrazolo[4,3-d]pyrimidine-3-carboxylate

: 624-78-2
N-Ethylmethylamine

: C21H25F3N6O3

Conditions

Conditions	Yield
With cesium fluoride In dimethyl sulfoxide at 120℃; for 12h;	96%

: 624-78-2
N-Ethylmethylamine

: 536-74-3
phenylacetylene

: C11H15N

Conditions

Conditions	Yield
With C18H17N3Ni In toluene at 75℃; for 6h;	96%
With C17H15N3Pd In toluene at 75℃; for 6h;	93%

: 7170-36-7
6-(methoxycarbonyl)pyridine-2-carboxylic acid

: 624-78-2
N-Ethylmethylamine

: 6-(ethyl(methyl)carbamoyl)picolinic acid methyl ester

Conditions

Conditions	Yield
With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 5h;	96%

N-Ethylmethylamine Specification

The N-Ethylmethylamine, with the CAS registry number 624-78-2 and EINECS registry number 210-862-1, has the systematic name and IUPAC name of N-methylethanamine. And the molecular formula of this chemical is C₃H₉N. It is a kind of clear colorless to light yellow liquid which is also hygroscopic. And it should be stored at 0-6°C.

The physical properties of N-Ethylmethylamine are as following: (1)ACD/LogP: 0.10; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3; (4)ACD/LogD (pH 7.4): -2.81; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 3.24 Å²; (13)Index of Refraction: 1.367; (14)Molar Refractivity: 19.54 cm³; (15)Molar Volume: 86.8 cm³; (16)Polarizability: 7.74×10^-24cm³; (17)Surface Tension: 18.2 dyne/cm; (18)Density: 0.68 g/cm³; (19)Enthalpy of Vaporization: 28.16 kJ/mol; (20)Boiling Point: 36.7 °C at 760 mmHg; (21)Vapour Pressure: 488 mmHg at 25°C.

Uses of N-Ethylmethylamine: It can react with trifluoroacetic acid anhydride to produce N-ethyl-N-methyltrifluoroacetamide. This reaction will need solvent diethyl ether.

N-Ethylmethylamine can react with trifluoroacetic acid anhydride to produce N-ethyl-N-methyltrifluoroacetamide

You should be cautious while dealing with this chemical. It is a kind of highly flammable chemical ehich may also cause severe burns. And it is also harmful by inhalation, in contact with skin and if swallowed. Therefore, you had better take the following instructions: Wear suitable protective clothing, gloves and eye/face protection, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice; In case of accident or if you feel unwell, seek medical advice immediately (show label where possible); Keep away from sources of ignition - No smoking.

You can still convert the following datas into molecular structure:
(1)SMILES: N(CC)C
(2)InChI: InChI=1/C3H9N/c1-3-4-2/h4H,3H2,1-2H3
(3)InChIKey: LIWAQLJGPBVORC-UHFFFAOYAE

Product Name

N-Ethylmethylamine

Synthetic route

N-Ethylmethylamine Specification

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