Dipropylamine supplier | CasNO.142-84-7

Name
Dipropylamine
EINECS 205-565-9
CAS No. 142-84-7
Article Data114
CAS DataBase
Density 0.741 g/cm³
Solubility soluble in water
Melting Point -63 °C
Formula C₆H₁₅N
Boiling Point 108.8 °C at 760 mmHg
Molecular Weight 101.192
Flash Point 3.9 °C
Transport Information UN 2383 3/PG 2
Appearance clear, colorless liquid
Safety 16-26-36/37/39-45
Risk Codes 11-20/21/22-35
Molecular Structure
Hazard Symbols F,C
Synonyms Dipropylamine(8CI);Di-n-propylamine;Dipropanamine;N,N-Dipropylamine;N-Propyl-1-propanamine;n-Dipropylamine;
PSA 12.03000
LogP 1.78690

Synthetic route

: 25070-76-2
benzyl diallylcarbamate

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In tetrahydrofuran-d8 at 20℃; for 24h;	100%
With hydrogen In d(4)-methanol at 20℃; under 760.051 Torr; for 24h;	100%
With hydrogen In methanol; d(4)-methanol at 40℃; under 760.051 Torr; for 1h; Reagent/catalyst; chemoselective reaction;	100%
With hydrogen In d(4)-methanol at 20℃; under 2280.15 Torr; for 24h; Reagent/catalyst; chemoselective reaction;

: 107-10-8
propylamine

: 74-85-1
ethene

: 201230-82-2
carbon monoxide

A: 102-69-2
tri-n-propylamine

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
di(rhodium)tetracarbonyl dichloride In ethanol at 119℃; under 44253.5 Torr; for 1h;	A 1% B 99%
di(rhodium)tetracarbonyl dichloride In ethanol at 119℃; under 44253.5 Torr; for 1h;	A 2% B 98%

...Expand

: C10H19NO2

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With titanium(IV) isopropylate; chloro-trimethyl-silane; magnesium In tetrahydrofuran at 50℃; for 24h;	94%

: 107-12-0
propiononitrile

A: 102-69-2
tri-n-propylamine

B: 7707-70-2
N-propylidenepropylamine

C: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With hydrogen at 220℃;	A 8.5% B 2.5% C 89%
With hydrogen at 240℃; Temperature; Flow reactor;	A 13% B 2.5% C 80%

...Expand

: 64935-06-4
3-Dipropylamino-7-hydroxy-heptanenitrile

A: 75394-84-2
(+/-)-2-perhydro-2H-pyran-2-ylethanenitrile

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With potassium tert-butylate at 180℃;	A 88% B 61%

: 621-64-7
N-nitroso-N,N-dipropylamine

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With isocyanate de chlorosulfonyle In diethyl ether for 10h; Ambient temperature;	69%

: 75162-84-4
1-dipropylamino-4-methyl-3-penten-1-ynamine

: 107-15-3
ethylenediamine

A: 142-84-7
di-n-propylamine

B: 87703-38-6
2-(3-methyl-2-butenyl)imidazoline

Conditions

Conditions	Yield
With sulfuric acid In 1,4-dioxane	A n/a B 68%

...Expand

: 75162-84-4
1-dipropylamino-4-methyl-3-penten-1-ynamine

: 141-43-5
ethanolamine

A: 87703-36-4
2-(3-methyl-2-butenyl)oxazoline

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With sulfuric acid In 1,4-dioxane at 100℃; for 4h;	A 65% B n/a

...Expand

: 70490-69-6
1-dipropylamino-3-penten-1-yne

: 107-15-3
ethylenediamine

A: 142-84-7
di-n-propylamine

B: 87703-37-5
2-(2-butenyl)imidazoline

Conditions

Conditions	Yield
With sulfuric acid In 1,4-dioxane	A n/a B 60%

...Expand

: 7707-70-2
N-propylidenepropylamine

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ethanol; calcium at 20℃; for 24h;	55%

: 70490-69-6
1-dipropylamino-3-penten-1-yne

: 141-43-5
ethanolamine

A: 87703-35-3
2-(2-butenyl)oxazoline

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With sulfuric acid In 1,4-dioxane at 100℃; for 4h;	A 52% B n/a

...Expand

: 5848-64-6
Tris(di-n-propylamino)phosphine

: 131471-75-5
C14H11ClN4OS

A: 15545-56-9
N-phenyl-N',N'-di(n-propyl)urea

B: 131471-73-3
C25H45ClN6P2S

C: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
at 125℃; under 130 Torr;	A n/a B 11.5% C n/a

...Expand

: 5848-64-6
Tris(di-n-propylamino)phosphine

: 131471-74-4
1-(6-Methyl-2-benzothiazolyl)-4-phenylsemicarbazide

A: 15545-56-9
N-phenyl-N',N'-di(n-propyl)urea

B: 131471-70-0
C26H48N6P2S

C: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
at 125℃; under 130 Torr;	A n/a B 11% C n/a

...Expand

: 71-23-8
propan-1-ol

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ammonia at 420℃; ueber Silicagel;

: 107-10-8
propylamine

: 102-69-2
tri-n-propylamine

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With alumina hydrate; ammonia at 370℃; under 139746 Torr;

: 67-62-9
O-Methylhydroxylamin

: 927-77-5
n-propylmagnesium bromide

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With diethyl ether at -10℃; zuletzt bei Siedetemperatur;

: 540-54-5
1-Chloropropane

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ethanol; ammonia; water at 100℃; under 5148.6 - 7355.08 Torr;
With ethanol; ammonia; water at 100℃; under 5148.6 - 7355.08 Torr;

: 1531-36-8
dipropylamine-N-carbonitrile

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With sulfuric acid; hydrogen

: 628-91-1
di-n-propyl zinc

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With chloroamine; Petroleum ether at -30℃;

: 106-94-5
propyl bromide

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ethanol; ammonia; water at 100℃; under 5148.6 - 7355.08 Torr;
With ethanol; ammonia; water at 100℃; under 5148.6 - 7355.08 Torr;

: 447429-10-9
N,N-diisopropyl-N'-propyl-urea

: 107-21-1
ethylene glycol

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
at 100℃; Rate constant;

: 107-10-8
propylamine

: 123-38-6
propionaldehyde

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With nickel at 162 - 195℃; under 36775.4 - 73550.8 Torr; Hydrogenation;

: 123-38-6
propionaldehyde

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With methanol; ammonia; nickel at 155 - 165℃; under 51485.6 Torr; Hydrogenation;

: 108-03-2
1-Nitropropane

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ethanol; nickel at 40 - 50℃; under 4413.05 - 80905.8 Torr; Hydrogenation;
With hydrogenchloride; iron at 100℃;
With nickel-cobalt-cadmium-chromium at 390 - 400℃;
With ethanol; nickel at 100℃; under 102971 Torr; Hydrogenation;

: 107-02-8
acrolein

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With Ni-doped silica; ammonia; hydrogen at 125℃;
With Ni-doped silica; ammonia; hydrogen at 125℃;

: 107-12-0
propiononitrile

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With ammonia; nickel at 100 - 150℃; under 73550.8 Torr; Hydrogenation;
With hydrogenchloride; platinum under 2206.5 Torr; Hydrogenation;
With 5%-palladium/activated carbon; ammonium formate In ethanol at 20℃;

: 107-12-0
propiononitrile

A: 107-10-8
propylamine

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
With hydrogen; nickel boride; silica gel In ethanol at 70℃; under 4560 Torr; Product distribution; Kinetics; other nickel catalyst, different times, solvents, and temp.;
With hydrogen; nickel In methanol at 70℃; under 7500.6 Torr; Product distribution; also in presence of amines, competition with cyclohexene;
With nickel at 130 - 140℃; Hydrogenation.unter Normaldruck;
With ethanol; ammonia; nickel at 125℃; under 44130.5 Torr; Hydrogenation;

: 447429-10-9
N,N-diisopropyl-N'-propyl-urea

: 100-51-6
benzyl alcohol

: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
at 100℃; Rate constant;

: 60-29-7
diethyl ether

: 5775-34-8
N,N-Dipropyl-chloramine

: 6921-34-2
benzylmagnesium chloride

A: 20441-12-7
N-benzyl-N,N-dipropylamine

B: 142-84-7
di-n-propylamine

Conditions

Conditions	Yield
at 5℃;

...Expand

: 142-84-7
di-n-propylamine

: 621-64-7
N-nitroso-N,N-dipropylamine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid; sodium nitrite In dichloromethane at 20℃;	100%
With dinitrogen trioxide Kinetics; Rate constant; Thermodynamic data; ΔH(excit.);
With hydrogenchloride; sodium nitrite

: 74-85-1
ethene

: 201230-82-2
carbon monoxide

: 142-84-7
di-n-propylamine

: 102-69-2
tri-n-propylamine

Conditions

Conditions	Yield
di(rhodium)tetracarbonyl dichloride In ethanol at 115℃; under 37503 Torr; for 1.5h;	100%

...Expand

: 142-84-7
di-n-propylamine

: 63587-45-1
Toluene-4-sulfonic acid 1-(toluene-4-sulfonyl)-piperidin-2-ylmethyl ester

: 186790-30-7
Dipropyl-[1-(toluene-4-sulfonyl)-piperidin-2-ylmethyl]-amine

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene for 48h; Heating;	100%

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

: 142-84-7
di-n-propylamine

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

Conditions

Conditions	Yield
In water Heating;	100%

: 142-84-7
di-n-propylamine

: 4-[phenyl(exo-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)amino]benzoic acid

: 347888-67-9
N,N-di-n-propyl-4-[phenyl(exo-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)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%

: 142-84-7
di-n-propylamine

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

: 287720-98-3
4-[(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-phenyl-amino]-N,N-dipropyl-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%

: 24801-88-5
3-(triethoxypropyl) isocyanate

: 142-84-7
di-n-propylamine

: N-di-n-propyl-N'-[3-(triethoxysilyl)propyl]urea

Conditions

Conditions	Yield
In hexane at 20℃; for 3h;	100%

: 920490-05-7
6-(2-hydroxyethyl)-2-(methylthio)-4-pyrimidinyl 4-methyl-1-benzenesulfonate

: 142-84-7
di-n-propylamine

: C13H23N3OS

Conditions

Conditions	Yield
In tetrahydrofuran at 70℃; for 48h;	100%

: 1955-46-0
5-nitro-1,3-benzenedicarboxylic acid, monomethyl ester

: 142-84-7
di-n-propylamine

: 328284-59-9
5-nitro-N,N-dipropyl-isophthalamic acid methyl ester

Conditions

Conditions	Yield
Stage #1: 5-nitro-1,3-benzenedicarboxylic acid, monomethyl ester With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 1h; Stage #2: di-n-propylamine In dichloromethane at 20℃; for 0.5h;	100%
With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 5h;	75%

: 1071600-29-7
2-hydroxy-2-(4-methoxybenzoyl)cyclohexane-1-carboxylic acid

: 142-84-7
di-n-propylamine

: 1071600-59-3
2-hydroxy-2-(4-methoxy-benzoyl)-cyclohexanecarboxylate dipropyl-ammonium

Conditions

Conditions	Yield
In toluene at 65℃; Heating / reflux;	100%

: 1114592-18-5
tert-butyl (4-{[(6-chloropyrimidin-4-yl)carbonyl]amino}benzyl)carbamate

: 142-84-7
di-n-propylamine

: tert-butyl [4-({[6-(dipropylamino)pyrimidin-4-yl]carbonyl}amino)benzyl]carbamate

Conditions

Conditions	Yield
With triethylamine In ethanol at 100℃; for 2.5h; microwave irradiation; sealed tube;	100%

: 1338931-99-9
5,7-dichloro-6-methoxypyrazolo[1,5-a]pyrimidine

: 142-84-7
di-n-propylamine

: 1338932-08-3
(5-chloro-6-methoxypyrazolo[1,5-a]pyrimidin-7-yl)dipropylamine

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 20℃; chemoselective reaction;	100%

: 142-84-7
di-n-propylamine

: 682-30-4
Diethyl vinylphosphonate

: 1415210-87-5
C12H28NO3P

Conditions

Conditions	Yield
With water at 100℃; for 0.0833333h; Inert atmosphere;	100%

: naphtho[2,3-d][1,3]dioxole-6-carboxylic acid

: 142-84-7
di-n-propylamine

: 1616610-11-7
N,N-dipropylnaphtho[2,3-d][1,3]dioxole-6-carboxamide

Conditions

Conditions	Yield
Stage #1: naphtho[2,3-d][1,3]dioxole-6-carboxylic acid With oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; Stage #2: di-n-propylamine In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃;	100%

: tert-butyl 2-hydroxy-4-(2-oxoethyl)-2,3-dihydro-1H-indole-1-carboxylate

: 142-84-7
di-n-propylamine

: tert-butyl 4-(2-(dipropylamino)ethyl)-2-hydroxyindoline-1-carboxylate

Conditions

Conditions	Yield
Stage #1: tert-butyl 2-hydroxy-4-(2-oxoethyl)-2,3-dihydro-1H-indole-1-carboxylate; di-n-propylamine With acetic acid In dichloromethane for 0.75h; Stage #2: With sodium cyanoborohydride In dichloromethane for 2h;	100%

: 109687-65-2
(S)-(-)-1,1-dimethylethyl <3-methyl-1-<<(methylsulfonyl)oxy>methyl>butyl>carbamate

: 142-84-7
di-n-propylamine

: (S)-tert-butyl 1-(dipropylamino)-4-methylpentan-2-ylcarbamate

Conditions

Conditions	Yield
With triethylamine In acetonitrile at 20℃; for 40h; Inert atmosphere;	100%

: 126301-19-7, 134807-64-0, 109687-66-3
(2S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropyl methanesulfonate

: 142-84-7
di-n-propylamine

: (S)-tert-butyl 1-(dipropylamino)-3-phenylpropan-2-ylcarbamate

Conditions

Conditions	Yield
With triethylamine In acetonitrile at 20℃; for 40h; Inert atmosphere;	100%

: 126301-16-4
(2S)-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

: 142-84-7
di-n-propylamine

: (S)-tert-butyl 1-(dipropylamino)propan-2-ylcarbamate

Conditions

Conditions	Yield
With triethylamine In acetonitrile at 20℃; for 40h; Inert atmosphere;	100%

: 142-84-7
di-n-propylamine

: 5326-84-1
N,N-dipropylamine hydrochloride

Conditions

Conditions	Yield
With hydroxylamine hydrochloride In ethanol for 2h; Reflux;	100%

: 112-77-6
(Z)-9-octadecenoyl chloride

: 142-84-7
di-n-propylamine

: 13653-24-2
N,N-dipropyloleamide

Conditions

Conditions	Yield
In benzene for 1h; Ambient temperature;	99.5%

: 142-84-7
di-n-propylamine

: 388071-08-7
methyl 3-bromo-5-(dipropylcarbamoyl)benzoate

Conditions

Conditions	Yield
Stage #1: 3-bromo-5-(methoxycarbonyl)benzoic acid With HATU In N,N-dimethyl-formamide at 20℃; for 0.166667h; Stage #2: di-n-propylamine In N,N-dimethyl-formamide at 20℃;	99.5%
Multi-step reaction with 3 steps 1: 75 percent / CDI / CH2Cl2 / 5 h / 20 °C 2: 70 percent / H2 / Pd/C / 18 h / 2585.81 Torr 3: 75 percent / butyl nitrite; copper(II) bromide / acetonitrile / 2 h / 20 °C View Scheme

: 75-15-0
carbon disulfide

: 142-84-7
di-n-propylamine

: 2556-42-5
tetrapropyl thiuram disulfide

Conditions

Conditions	Yield
With oxygen In isopropyl alcohol at 50℃; under 1275.13 Torr; for 1.41667h; Autoclave;	99.2%
Stage #1: carbon disulfide; di-n-propylamine With potassium hydroxide In tetrahydrofuran; water at 20℃; for 12h; Stage #2: With iodine In tetrahydrofuran; methanol; water at 20℃; for 1h;	73%
With oxygen; eosin Y disodium salt In methanol under 3750.38 Torr; for 0.333333h; Solvent; Flow reactor; Irradiation; Green chemistry;	69%

: 10130-89-9
p-carboxyphenylsulfonyl chloride

: 142-84-7
di-n-propylamine

: 57-66-9
4-[(dipropylamino)sulfonyl]benzoic acid

Conditions

Conditions	Yield
In dichloromethane at 0 - 20℃; for 18h;	99%
With sodium hydrogencarbonate In water; acetone at 25℃; Schotten-Baumann Reaction; Flow reactor;	78%

: 142-84-7
di-n-propylamine

: 624-83-9
methyl isocyanate

: 36614-21-8
1,1-dipropyl-3-methylurea

Conditions

Conditions	Yield
In diethyl ether cooling;	99%

: 50-00-0
formaldehyd

: 142-84-7
di-n-propylamine

: 536-74-3
phenylacetylene

: 153396-18-0
3-phenyl-N,N-dipropylprop-2-yn-1-amine

Conditions

Conditions	Yield
With Cu(2-hydroxypyrimidinolate)2 In 1,4-dioxane at 39.84℃; for 21h; Inert atmosphere;	99%
With copper(l) iodide In water; dimethyl sulfoxide at 30℃; for 5h;	87%
With copper(l) iodide In 1,4-dioxane Heating;

...Expand

: 142-84-7
di-n-propylamine

: 86657-79-6
(4aS,9bR)-4-[1-Dimethylamino-meth-(E)-ylidene]-8,9b-dimethyl-1,4,4a,9b-tetrahydro-2H-dibenzofuran-3-one

: 86657-94-5
(4aS,9bR)-4-[1-Dipropylamino-meth-(E)-ylidene]-8,9b-dimethyl-1,4,4a,9b-tetrahydro-2H-dibenzofuran-3-one

Conditions

Conditions	Yield
In benzene for 8h; Heating;	99%

: 2516-96-3
2-chloro-5-nitrobenzoic acid

: 142-84-7
di-n-propylamine

: 2-(dipropylamino)-5-nitrobenzoic acid

Conditions

Conditions	Yield
at 100℃; for 0.0833333h; microwave irradiation;	99%
With copper; potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.333333h; Ullmann condensation; ultrasonic irradiation;	79%

: 1878-69-9
3-iodophenylacetic acid

: 142-84-7
di-n-propylamine

: 865178-30-9
2-(3-iodo-phenyl)-N,N-dipropyl-acetamide

Conditions

Conditions	Yield
With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 20h;	99%

Dipropylamine Chemical Properties

IUPAC: N-propylpropan-1-amine
Molecular Formula of Dipropylamine (CAS NO.142-84-7): C₆H₁₅N
Molecular Weight: 101.19
Synonyms of Dipropylamine (CAS NO.142-84-7): n,n-dipropylamine 1-Propanamine, N-propyl- ; Di-n-propylamine ; Dipropylamine ; Dipropylamine [UN2383] [Flammable liquid] ; RCRA waste no. U110 ; UN2383
Refractive index: n20/D 1.4049(lit.)
CAS NO: 142-84-7
Polar Surface Area: 3.24 Å²
Index of Refraction: 1.405
Molar Refractivity: 33.44 cm³
Molar Volume: 136.3 cm³
Surface Tension: 23 dyne/cm
Flash Point: 3.9 °C
Enthalpy of Vaporization: 33.47 kJ/mol
Index of Refraction: 1.405
Density: 0.741 g/cm³Boiling Point: 108.8 °C at 760 mmHg
Vapour Pressure: 25.5 mmHg at 25°C
Stability: Stable. Highly flammable. Incompatible with strongoxidizing agents
The Structure of Dipropylamine (CAS NO.142-84-7):

Dipropylamine Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mammal (species unspecified)	LC50	inhalation	4400mg/m3 (4400mg/m3)		Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 14, Pg. 80, 1975.
mammal (species unspecified)	LD50	unreported	600mg/kg (600mg/kg)		Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 14, Pg. 80, 1975.
mouse	LC50	inhalation	3070mg/m3/2H (3070mg/m3)		"Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 63, 1982.
mouse	LD50	unreported	320mg/kg (320mg/kg)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 35(4), Pg. 103, 1970.
rabbit	LD50	skin	925mg/kg (925mg/kg)		National Technical Information Service. Vol. OTS0535430,
rabbit	LD50	subcutaneous	1250mg/kg (1250mg/kg)		"Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 434, 1986.
rat	LC50	inhalation	4400mg/m3/4H (4400mg/m3)		"Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 63, 1982.
rat	LD50	oral	300mg/kg (300mg/kg)	BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: MUSCLE WEAKNESS	National Technical Information Service. Vol. OTS0544865,
rat	LD50	unreported	280mg/kg (280mg/kg)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 35(4), Pg. 103, 1970.
rat	LDLo	intraperitoneal	75mg/kg (75mg/kg)		Farmakologiya i Toksikologiya Vol. 31, Pg. 238, 1968.

Dipropylamine Consensus Reports

Reported in EPA TSCA Inventory.

Dipropylamine Safety Profile

Poison by ingestion. Moderately toxic by skin contact and inhalation. A skin irritant. A very dangerous fire hazard, when exposed to heat or flame. Can react with oxidizers. Explosion hazard is unknown. Keep away from heat and open flame. To fight fire, use foam, CO₂, dry chemical. When heated to decomposition it emits toxic fumes of NO_x.
Safety Information of Dipropylamine (CAS NO.142-84-7):
Hazard Codes: F : ,C
Risk Statements: 11-20/21/22-35 ( Highly Flammable ; Harmful by inhalation, in contact with skin and if swallowed ; Causes severe burns
Safety Statements 16-26-36/37/39-45 [Keep away from sources of ignition - No smoking ; In case of contact with eyes, rinse immediately with plenty of water and seek medical advice ; Wear suitable protective clothing, gloves and eye/face protection ; In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) ] RIDADR UN 2383 3/PG 2
WGK Germany :1
RTECS : JL9200000
HazardClass :3
PackingGroup: II

Dipropylamine Standards and Recommendations

DOT Classification: 3; Label: Flammable Liquid

Product Name

Dipropylamine

Synthetic route

Dipropylamine Chemical Properties

Dipropylamine Toxicity Data With Reference

Dipropylamine Consensus Reports

Dipropylamine Safety Profile

Dipropylamine Standards and Recommendations

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