Ethylamine supplier | CasNO.75-04-7

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Name
Ethylamine
EINECS 200-834-7
CAS No. 75-04-7
Article Data525
CAS DataBase
Density 0.691 g/cm³
Solubility miscible in water
Melting Point -81 °C
Formula C₂H₇N
Boiling Point 14.2 °C at 760 mmHg
Molecular Weight 45.0843
Flash Point -17 °C
Transport Information UN 2733 3/PG 1
Appearance light yellow liquid
Safety 26-29-16-45-36/37-7
Risk Codes 12-36/37-19-39/23/24/25-23/24/25-11
Molecular Structure
Hazard Symbols F+,Xi,T,F
Synonyms Ethylamine(7CI,8CI);1-Aminoethane;Aminoethane;Monoethylamine;R 631;n-Ethylamine;
PSA 26.02000
LogP 0.66530

Synthetic route

: 75-05-8
acetonitrile

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With sodium tetrahydroborate In water; dimethyl sulfoxide at 60℃; for 4.5h; High pressure; Green chemistry;	99.9%
With borane-ammonia complex; copper cobaltite In methanol; water at 50℃; under 1125.11 Torr; for 5h; Catalytic behavior; Reagent/catalyst; Pressure; Concentration; Sealed tube;	98%
With hydrogen In ethanol at 99.84℃; under 22502.3 Torr; Autoclave;	81%

: 79-24-3
Nitroethane

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With borane-ammonia complex In methanol; water at 20℃; for 0.0833333h;	99%
With ammonia borane; Pd/MIL-101 In methanol; water at 20℃; for 0.025h;	99%
With sodium tetrahydroborate In methanol; water at 20℃; for 0.0666667h; Sealed tube; Green chemistry;	99%

: 79-24-3
Nitroethane

12percent nickel/Al-SBA-15 fiber: 12percent nickel/Al-SBA-15 fiber

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction;	99%

: 107-12-0
propiononitrile

: 75-04-7
ethylamine

Conditions

Conditions	Yield
Stage #1: propiononitrile In methanol; water at 20℃; for 0.0833333h; Stage #2: With ammonia borane In methanol; water at 20℃;	98%

: 79-24-3
Nitroethane

A: 75-04-7
ethylamine

B: 624-81-7
ethylhydroxylamine

Conditions

Conditions	Yield
With hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; for 2h; Catalytic behavior; Reagent/catalyst;	A 6% B 94%
Pt-Rh catalysts Product distribution; electrochemical reduction;
With sulfuric acid; palladium Product distribution; electrocatalytic hydrogenation, oth. catalysts;
With 5% Pd/SiO2; hydrogen In isopropyl alcohol at 20℃; under 750.075 Torr; for 2h;	A 9 %Spectr. B 91 %Spectr.

: 5300-22-1
(R/S)-2-(ethylamino)-1-phenylethanol

A: 52500-61-5
2-hydroxy-1-phenylpropylamine

B: 50-00-0
formaldehyd

C: 100-52-7
benzaldehyde

D: 75-04-7
ethylamine

E: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 1.9% B 67% C 75% D 79% E 10%

...Expand

: 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

: 19528-69-9
{(C2H5NH2)2BH2}(1+)*{SC2H5}(1-)={(C2H5NH2)2BH2}{SC2H5}

A: 7360-03-4
N,N',N''-triethylborazine

B: 75-04-7
ethylamine

C: 856627-30-0
ethylamine borane complex

D: 75-08-1
ethanethiol

Conditions

Conditions	Yield
In neat (no solvent) pyrolysis;;	A 20% B n/a C 36% D 75%
In neat (no solvent)

...Expand

: 100-37-8
2-(Diethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 109-89-7
diethylamine

E: 110-73-6
2-(Ethylamino)ethanol

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 5% B 1.6% C 72% D 20% E 73%

...Expand

: 623-76-7
N,N'-diethylurea

: 18522-92-4
sodium p-toluenesulfonamide

A: 1467-23-8
N-(ethylcarbamoyl)-4-methylbenzenesulfonamide

B: 75-04-7
ethylamine

Conditions

Conditions	Yield
at 145℃; for 5h; Product distribution; other time;;	A 71.6% B n/a
at 145℃; for 5h;	A 71.6% B n/a

...Expand

: 82922-12-1
2-Diethylamino-pentan-3-ol

A: 75-04-7
ethylamine

B: 75-07-0
acetaldehyde

C: 123-38-6
propionaldehyde

: 100910-76-7
2-Ethylamino-pentan-3-ol

E: 109-89-7
diethylamine

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A n/a B 70% C 36% D n/a E 46%

...Expand

: 82922-13-2
2-(ethylamino)-2-methylpropanol hydrochloride

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 124-68-5
2-Amino-2-methyl-1-propanol

D: 75-07-0
acetaldehyde

E: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 50% B 44% C 14% D 26% E 66%

...Expand

: 82922-13-2
2-(ethylamino)-2-methylpropanol hydrochloride

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 124-68-5
2-Amino-2-methyl-1-propanol

D: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 50% B 44% C 14% D 66%

...Expand

: 107-29-9
Acetaldehyde oxime

: 75-04-7
ethylamine

Conditions

Conditions	Yield
With ammonium formate; zinc In methanol for 0.05h; Heating;	62%
With ammonium amalgam
With ammonium formate; magnesium In methanol at 20℃; for 0.666667h;

: 2683-58-1
1-diethylamino-butan-2-ol

A: 50-00-0
formaldehyd

B: 68058-17-3
1-ethylamino-butan-2-ol

C: 75-04-7
ethylamine

D: 75-07-0
acetaldehyde

E: 123-38-6
propionaldehyde

F: 109-89-7
diethylamine

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 17% B 59% C 3% D 60% E 18% F 32%

...Expand

: trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0)

: 55-18-5
N-Nitrosodiethylamine

A: 74-85-1
ethene

: trans-bis[1,2-bis(diphenylphosphino)ethane]hydroxo(nitrosyl)molybdenum-tetrahydrofuran (1/2)

C: 7727-37-9
nitrogen

D: 75-04-7
ethylamine

Conditions

Conditions	Yield
With K2CO3; THF In tetrahydrofuran Irradiation (UV/VIS); Et2NNO and K2CO3 added to soln. of Mo complex in THF, heated under reflux under N2 with W-light irrdn. for 4 h; filtered hot, cooled to room temp., crystals recrystd. from THF; elem. anal.;	A n/a B 60% C n/a D n/a

...Expand

: 38451-07-9
1,6-diethyl-2,5-dithiobiurea

A: 75-04-7
ethylamine

B: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A n/a B 56%

: 86465-00-1
1-Ethoxy-3-ethylamino-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 4% B 55% C 53%

...Expand

: 86464-98-4
1-Cyclohexyloxy-3-ethylamino-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 108-93-0
cyclohexanol

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 5% B 54% C 55% D 18%

...Expand

: 58461-93-1
1-ethylamino-3-phenoxy-propan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 75-07-0
acetaldehyde

D: 108-95-2
phenol

Conditions

Conditions	Yield
With chlorine dioxide In water for 1h; Product distribution; Ambient temperature;	A 3% B 49% C 50% D 30%

...Expand

: 64-17-5
ethanol

: 112-53-8
1-dodecyl alcohol

: 75-05-8
acetonitrile

A: 112-40-3
dodecane

B: 74-84-0
ethane

C: 35902-57-9
N-n-dodecyl-ethylamine

D: 4271-27-6
diethyllaurylamine

E: 75-04-7
ethylamine

F: 121-44-8
triethylamine

Conditions

Conditions	Yield
With hydrogen; aluminum oxide; copper at 240℃; under 7600 Torr; Product distribution; other catalyst and composition;	A n/a B n/a C 15% D 30% E n/a F 50%

...Expand

: 110-73-6
2-(Ethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 141-43-5
ethanolamine

D: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 14% B 43% C 45% D 44%

...Expand

: 110-73-6
2-(Ethylamino)ethanol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 141-43-5
ethanolamine

D: 75-07-0
acetaldehyde

E: 141-46-8
Glycolaldehyde

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 14% B 43% C 45% D 44% E n/a

...Expand

: 125908-31-8
1-ethyl-6-tolyl-2,5-dithiobiurea

A: 14731-25-0
2-(4'-methylphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 106-49-0
p-toluidine

C: 75-04-7
ethylamine

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 44% B n/a C n/a D 31%

...Expand

: 73825-96-4
1-(ethylamino)-2-methylpropan-2-ol

A: 75-04-7
ethylamine

B: 2854-16-2
1-Amino-2-methyl-propan-2-ol

C: 75-07-0
acetaldehyde

D: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; anodic oxidation, pH 10, carbonate buffer; Further byproducts given;	A 35% B 18% C 34% D 43%

...Expand

: 73825-96-4
1-(ethylamino)-2-methylpropan-2-ol

A: 50-00-0
formaldehyd

B: 75-04-7
ethylamine

C: 2854-16-2
1-Amino-2-methyl-propan-2-ol

D: 75-07-0
acetaldehyde

E: 67-64-1
acetone

Conditions

Conditions	Yield
With water at 25℃; Product distribution; Mechanism; anodic oxidation, carbonate buffer, pH 10; effect of substituents investigated with different types of β-alkanolamines;	A 18% B 35% C 18% D 34% E 43%

...Expand

: 125908-34-1
1-ethyl-6-(4'-ethoxyphenyl)-2,5-dithiobiurea

A: 68161-60-4
2-(4'-ethoxyphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 75-04-7
ethylamine

C: 156-43-4
4-Ethoxyaniline

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 41% B n/a C n/a D 32%

...Expand

: 125908-33-0
1-ethyl-6-(4'-methoxyphenyl)-2,5-dithiobiurea

A: 37844-24-9
2-(4'-methoxyphenylamino)-Δ2-1,3,4-thiadiazoline-5-thione

B: 104-94-9
4-methoxy-aniline

C: 75-04-7
ethylamine

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A 40% B n/a C n/a D 34%

...Expand

: 61784-88-1
1-ethyl-6-phenyl-2,5-dithiobiurea

A: 75-04-7
ethylamine

B: 62-53-3
aniline

C: 10253-83-5
5-phenylamino-3H-[1,3,4]thiadiazole-2-thione

D: 13625-52-0
4-ethyl-[1,2,4]triazolidine-3,5-dithione

Conditions

Conditions	Yield
With sodium hydroxide In water Heating;	A n/a B n/a C 38% D 33%

...Expand

: 123-56-8
Succinimide

: 75-04-7
ethylamine

: 3025-98-7
N-ethyl-succinic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; soid-gas reaction; ring cleavage;	100%
With water

: 5022-29-7
N-ethylphthalimide

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 555-16-8
4-nitrobenzaldehdye

: 75-04-7
ethylamine

: 25105-58-2
N-(p-nitrobenzylidene)ethylamine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%
With water
In ethanol at 50℃;
In tetrahydrofuran; ethanol at 20℃; for 12h; Inert atmosphere;
In ethanol at 20℃; for 12h;

: 3460-18-2
1,4-dibromo-2-nitrobenzene

: 75-04-7
ethylamine

: 56136-82-4
(4-bromo-2-nitrophenyl)ethylamine

Conditions

Conditions	Yield
In water at 100℃; for 24h; Sealed vessel;	100%

: 459-57-4
4-fluorobenzaldehyde

: 75-04-7
ethylamine

: 82605-86-5
(E)-N-(4-fluorobenzylidene)ethanamine

Conditions

Conditions	Yield
With magnesium sulfate In dichloromethane; water at 24.84℃; for 4h;	100%
In diethyl ether for 2h;	74%

: 100-44-7
benzyl chloride

: 75-04-7
ethylamine

: 14321-27-8
N-ethylbenzylamine

Conditions

Conditions	Yield
	100%

: 99735-46-3
methyl (3S)-1-<(R)-1-phenylethyl>-5-oxo-3-pyrrolidinecarboxylate

: 75-04-7
ethylamine

: (S)-5-Oxo-1-((R)-1-phenyl-ethyl)-pyrrolidine-3-carboxylic acid ethylamide

Conditions

Conditions	Yield
In water at -10℃; for 1h;	100%

: 115975-33-2
N,N-Dimethyl-2,4-bis(trifluoroacetyl)-1-naphthylamine

: 75-04-7
ethylamine

: 115975-37-6
1-[1-Ethylamino-4-(2,2,2-trifluoro-acetyl)-naphthalen-2-yl]-2,2,2-trifluoro-ethanone

Conditions

Conditions	Yield
In water; acetonitrile for 2h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 84054-96-6
ethyl 4-formyl-2-hydroxybenzoate

: 84054-99-9
4-[(Z)-Ethyliminomethyl]-2-hydroxy-benzoic acid ethyl ester

Conditions

Conditions	Yield
for 0.333333h;	100%

: 75-04-7
ethylamine

: 100890-40-2
1-Methyl-6-methylsulfanyl-2,4-dioxo-3-phenyl-1,2,3,4-tetrahydro-pyrimidine-5-carbonitrile

: 105736-29-6
6-Ethylamino-1-methyl-2,4-dioxo-3-phenyl-1,2,3,4-tetrahydro-pyrimidine-5-carbonitrile

Conditions

Conditions	Yield
In acetonitrile for 0.0833333h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 2,4,6,8-Tetrachloro-N,N''-diethyl-N',N',N''',N'''-tetramethyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C16H48N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: N,N''-Di-tert-butyl-2,4,6,8-tetrachloro-N',N'''-diethyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C20H56N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: 2,4,6,8-Tetrachloro-N,N''-diethyl-N',N'''-dimethyl-N',N'''-diphenyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine-2,4,6,8-tetraamine

: C26H52N12P4

Conditions

Conditions	Yield
In diethyl ether Heating;	100%

: 75-04-7
ethylamine

: 22113-86-6
ethylammonium nitrate

Conditions

Conditions	Yield
With nitric acid In water at 10℃; pH=7.3;	100%
With nitric acid In water for 1h; pH=7.3; Cooling with ice;	100%
With acide nitrique at 0℃;

: 27210-68-0
1-diethylamino-2,4-dinitronaphthalene

: 75-04-7
ethylamine

A: 27210-67-9
N-ethyl-2,4-dinitro-1-naphthylamine

B: 109-89-7
diethylamine

Conditions

Conditions	Yield
In water at 30℃; for 1h;	A 100% B n/a

...Expand

: 75-04-7
ethylamine

: 168697-54-9
tetraethyl ethylenebisbenzoyloxymalonate

: tetraethylamide of 1,2-ethylenebistartronic acid

Conditions

Conditions	Yield
In methanol at 20℃; for 72h;	100%

: 23596-82-9
3,4-bis(diphenylmethylene)-1,2-cyclobutanedione

: 75-04-7
ethylamine

: N-ethyl-3,4-bis(diphenylmethylene)succinimide

Conditions

Conditions	Yield
With bromine In tetrachloromethane for 0.5h; Ambient temperature;	100%

: 75-04-7
ethylamine

: 221636-53-9
N,N-dimethyl-5,7-bis(trifluoroacetyl)-8-quinolylamine

: 1-[8-Ethylamino-5-(2,2,2-trifluoro-acetyl)-quinolin-7-yl]-2,2,2-trifluoro-ethanone

Conditions

Conditions	Yield
With water In acetonitrile for 1h; Ambient temperature;	100%
With water In acetonitrile at 20℃; for 1h; Substitution;	100%

: 96-48-0
4-butanolide

: 75-04-7
ethylamine

: 42042-64-8
N-ethyl-4-hydroxybutanamide

Conditions

Conditions	Yield
In tetrahydrofuran at 50℃; for 22h;	100%
In tetrahydrofuran at 20℃; Acylation;
With ammonia In methanol at 20℃;

: 1121-89-7
piperidine-2,6-dione

: 75-04-7
ethylamine

: N-ethyl-glutaric diamide

Conditions

Conditions	Yield
at 80℃; under 600.048 - 750.06 Torr; Addition; soid-gas reaction; ring cleavage;	100%

: 524-38-9
N-hydroxyphthalimide

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 4702-13-0
N-phthaloylglycine

: 75-04-7
ethylamine

: 22011-24-1
N,N'-diethylphthalic diamide

Conditions

Conditions	Yield
at 20℃; under 600.048 - 750.06 Torr; Substitution; solid-gas reaction; ring cleavage;	100%

: 117-08-8
tetrachlorophthalic anhydride

: 75-04-7
ethylamine

: ethyl-tetrachlorophthalamic acid ethylammonium salt

Conditions

Conditions	Yield
under 750.06 Torr; Condensation; solid-gas reaction; ring cleavage;	100%

: 119-84-6
C6H4(CH2CH2C(O)O)

: 75-04-7
ethylamine

: ethyl-3-(2-hydroxyphenyl)-propionamide

Conditions

Conditions	Yield
at 0℃; under 150.012 Torr; Addition; solid-gas reaction; ring cleavage;	100%

: 123-08-0
4-hydroxy-benzaldehyde

: 75-04-7
ethylamine

: 4-[(ethylimino)methyl]phenol

Conditions

Conditions	Yield
at 0℃; under 187.515 Torr; Solid phase reaction; gas-solid reaction;	100%
With calcium oxide In ethanol; water at 20℃; for 2.5h;

: 21240-34-6
4,5-diphenyl-1,3-dioxol-2-one

: 75-04-7
ethylamine

: ethylcarbamic 1-phenylphenacylester

Conditions

Conditions	Yield
at 20℃; under 600.048 Torr; for 24h; Addition; solid-gas reaction; ring cleavage;	100%

: 75-04-7
ethylamine

: 556-61-6
methyl thioisocyanate

: 2489-77-2
1,1,3-trimethylthiourea

Conditions

Conditions	Yield
at 0℃; under 375.03 Torr; Addition; solid-gas reaction;	100%

: 75-04-7
ethylamine

: 100-10-7
4-dimethylamino-benzaldehyde

: 59488-00-5
4-[(ethylimino)methyl]-N,N-dimethylbenzeneamine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%

: 75-04-7
ethylamine

: 551-06-4
1-isothiocyanatonaphthalene

: 2742-61-2
1,1-dimethyl-3-naphthalene-1-yl-thiourea

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Addition; solid-gas reaction;	100%

: 75-04-7
ethylamine

: 642-31-9
9-anthracene aldehyde

: [1-Anthracen-9-yl-meth-(Z)-ylidene]-ethyl-amine

Conditions

Conditions	Yield
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction;	100%
In methanol for 9h; Reflux;	84%

Ethylamine Analytical Methods

The common method:Ethanol and ammonia are combined in the presence of an oxide catalyst:CH₃CH₂OH + NH₃ → CH₃CH₂NH₂ + H₂O
It is also produced by reductive amination of acetaldehyde.CH₃CHO + NH₃ + H₂ → CH₃CH₂NH₂ + H₂O
Ethylamine can be prepared by several other routes, but those are not economical.

Ethylamine Specification

The IUPAC name of Monoethylamine is ethanamine. With the CAS registry number 75-04-7, it is also named as 1-Aminoethane. The product's categories are Pharmaceutical Intermediates; Refrigerants; Alkylamines; Monofunctional & alpha, omega-Bifunctional Alkanes; Monofunctional Alkanes; Amines (Low Boiling point); Gas Cylinders; Synthetic Organic Chemistry, and the other registry numbers are 43031-21-6; 85404-16-6; 85404-22-4. Besides, it is light yellow liquid, which should be sealed in a cool and dry place at 2-8 °C. In addition, its molecular formula is C₂H₇N and molecular weight is 45.08.

The other characteristics of this product can be summarized as: (1)EINECS: 200-834-7; (2)ACD/LogP: -0.13; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): -3.23; (5)ACD/LogD (pH 7.4): -2.99; (6)ACD/BCF (pH 5.5): 1; (7)ACD/BCF (pH 7.4): 1; (8)ACD/KOC (pH 5.5): 1; (9)ACD/KOC (pH 7.4): 1; (10)#H bond acceptors: 1; (11)#H bond donors: 2; (12)#Freely Rotating Bonds: 1; (13)Index of Refraction: 1.372; (14)Molar Refractivity: 14.84 cm³; (15)Molar Volume: 65.2 cm³; (16)Surface Tension: 21.6 dyne/cm; (17)Density: 0.691 g/cm³; (18)Flash Point: -17 °C; (19)Melting Point: -81 °C; (20)Enthalpy of Vaporization: 26.17 kJ/mol; (21)Boiling Point: 14.2 °C at 760 mmHg; (22)Vapour Pressure: 1130 mmHg at 25 °C.

Preparation of Monoethylamine: this chemical can be prepared by the reaction of Ethanol with Ammonia in the presence of an oxide catalyst:
CH₃CH₂OH + NH₃ → CH₃CH₂NH₂+ H₂O

Uses of Monoethylamine: this chemical can be be oxidized to form Acetaldehyde. It is a precursor to many herbicides including atrazine and simazine. And it is widely used in chemical industry and organic synthesis. Additionally, it can react with [1,3]Dioxolan-2-one to get Ethyl-carbamic acid-(2-hydroxy-ethyl ester).

This reaction will occur at temperature of 20 °C for 1 hour. The yield is 92 %.

When you are using this chemical, please be cautious about it as the following: it is extremely flammable that may form explosive peroxides. Please keep away from sources of ignition. It is also toxic by inhalation, in contact with skin and if swallowed, so please keep container tightly closed. Moreover, it is danger of very serious irreversible effects, and irritating to eyes and respiratory system. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. And you should wear suitable protective clothing and gloves. Furthermore, please do not empty into drains. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)

People can use the following data to convert to the molecule structure.
(1)Canonical SMILES: CCN
(2)InChI: InChI=1S/C2H7N/c1-2-3/h2-3H2,1H3
(3)InChIKey: QUSNBJAOOMFDIB-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mammal (species unspecified)	LC50	inhalation	2300mg/m³ (2300mg/m³)		Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 14, Pg. 80, 1975.
rabbit	LD50	skin	390uL/kg (0.39mL/kg)		AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954.
rabbit	LDLo	intravenous	350mg/kg (350mg/kg)		"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1295, 1935.
rat	LC50	inhalation	5540ppm/1H (5540ppm)	SENSE ORGANS AND SPECIAL SENSES: CORNEAL DAMAGE: EYE LUNGS, THORAX, OR RESPIRATION: DYSPNEA	National Technical Information Service. Vol. OTS0538173,
rat	LD50	oral	400mg/kg (400mg/kg)		AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954.

Product Name

Ethylamine

Synthetic route

Ethylamine Analytical Methods

Ethylamine Specification

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