Isopropylamine supplier | CasNO.75-31-0

Name
Isopropylamine
EINECS 200-860-9
CAS No. 75-31-0
Article Data211
CAS DataBase
Density 0.719 g/cm³
Solubility soluble in water
Melting Point -101 °C
Formula C₃H₉N
Boiling Point 30.9 °C at 760 mmHg
Molecular Weight 59.1112
Flash Point ?26°F
Transport Information UN 1221 3/PG 1
Appearance colourless liquid
Safety 16-26-29
Risk Codes 12-36/37/38
Molecular Structure
Hazard Symbols F+,Xi
Synonyms 2-Propanamine;1-Methylethylamine;2-Aminopropane;2-Isopropylamine;2-Propylamine;Monoisopropylamine;NSC 62775;Propan-2-ylamine;sec-Propylamine;
PSA 26.02000
LogP 1.05380

Synthetic route

: 79-46-9
2-nitropropane

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With hydrogen In methanol; water at 140℃; under 30003 Torr; for 24h; Sealed tube; Autoclave;	97%
With [Zn(BH4)2(py)] In tetrahydrofuran for 0.8h; Heating;	94%
With poly(p-aminostyrene)-palladium(II); hydrogen In N,N-dimethyl-formamide at 70℃; under 760 Torr; for 6h;	91%

: 67-56-1
methanol

: Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

A: Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

B: 6843-66-9
dimethoxy(diphenyl)silane

C: 75-31-0
isopropylamine

Conditions

Conditions	Yield
In benzene-d6 at 20℃; for 24h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere;	A n/a B 97% C 74%

...Expand

: 67-64-1
acetone

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With ammonia; hydrogen at 153℃; under 760.051 Torr; Reagent/catalyst;	90.69%
With ammonia; nickel at 100℃; under 36775.4 - 55163.1 Torr; Hydrogenation;
With platinum on silica; ammonia at 240℃; Hydrogenation;

: 79-46-9
2-nitropropane

A: 75-31-0
isopropylamine

B: 5080-22-8
N-isopropylhydroxyamine

Conditions

Conditions	Yield
With hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; for 4h;	A 9% B 88%

: 4128-37-4
1,3-diisopropylurea

: 18522-92-4
sodium p-toluenesulfonamide

A: 5673-38-1
N-(isopropylcarbamoyl)-4-methylbenzenesulfonamide

B: 75-31-0
isopropylamine

Conditions

Conditions	Yield
at 170℃; for 5h; Product distribution; other time;;	A 78.2% B n/a
at 170℃; for 5h;	A 78.2% B n/a

...Expand

: 127-06-0
acetone oxime

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With ammonium formate; zinc In methanol for 0.05h; Heating;	70%
With nickel Hydrogenation.unter verschiedenen Bedingungen;
With aluminium amalgam

: 10475-45-3
bis(isopropylamino)phenylborane

A: (C6H5)BN(C3H7)

B: 75-31-0
isopropylamine

Conditions

Conditions	Yield
	A n/a B 65%
	A n/a B 65%

: 67-63-0
isopropyl alcohol

A: 75-31-0
isopropylamine

B: 108-18-9
diisopropylamine

C: 67-64-1
acetone

Conditions

Conditions	Yield
With ammonia; hydrogen at 160℃; under 760.051 Torr; for 0.5h; Catalytic behavior; Reagent/catalyst; Flow reactor; Inert atmosphere;	A 59.9% B n/a C n/a
With nitrogen; ammonia; hydrogen at 170℃; Concentration; Time; Reagent/catalyst;

...Expand

: 63465-11-2
Bis-(trifluormethyl)-bis-(trifluormethoxy)-sulfuran

: 75-04-7
ethylamine

A: 353-50-4
Carbonyl fluoride

B: 65756-36-7
hydrogen fluoride ethylamine

C: 75-31-0
isopropylamine

Conditions

Conditions	Yield
-78°C, 0.5 h;	A n/a B n/a C 56%

...Expand

: 67-56-1
methanol

: Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

A: methoxydiphenyl(isopropyl-amino)silane

B: Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

C: 6843-66-9
dimethoxy(diphenyl)silane

D: 75-31-0
isopropylamine

Conditions

Conditions	Yield
In benzene-d6 at 20℃; for 4h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere;	A 11% B 34% C 36% D 48%

...Expand

: 28227-41-0, 24764-90-7
1,4-diisopropyl-1,4-diazabuta-1,3-diene

: 613-73-0
1,2-phenylenediacetonitrile

A: 3029-30-9
naphthalene-1,4-dicarbonitrile

B: 75-31-0
isopropylamine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 136℃; for 1h;	A 43% B n/a

...Expand

: 56-41-7
L-alanin

A: 2749-11-3
(S)-Alaninol

B: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With phosphoric acid; hydrogen In water at 79.84℃; under 7500.75 - 60006 Torr; for 4h; Concentration; Reagent/catalyst;	A 42.2% B n/a
With sulfuric acid; hydrogen In water at 79.84℃; under 60006 Torr; for 2h; Catalytic behavior; Autoclave;

: 108-18-9
diisopropylamine

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
Stage #1: diisopropylamine With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h; Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior;	31.2%

: 3615-24-5
ramifenazone

A: 13359-68-7
N-Phenyl-N-(2-methylaminopropionyl)carbamic acid

B: 16945-58-7
Methyltartronic acid anilide methylamide

C: 75-31-0
isopropylamine

D: Methyltartronic acid anilide isopropylamide

Conditions

Conditions	Yield
In water for 1728h; Irradiation;	A 30% B 22.5% C n/a D 8%

...Expand

: 102-97-6
Benzyl-isopropyl-amin

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
Stage #1: Benzyl-isopropyl-amin With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h; Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior;	18.1%

: 75-30-9
2-iodo-propane

: 1074-82-4
potassium phtalimide

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
at 180 - 190℃; und Kochen des Reaktionsprodukts mit konz. HCl;

: 75-30-9
2-iodo-propane

: 151-50-8
potassium cyanide

A: 75-31-0
isopropylamine

B: 108-18-9
diisopropylamine

Conditions

Conditions	Yield
Behandeln des Reaktionsproduktes mit Salzsaeure;

...Expand

: 304-17-6
N-isopropylphthalimide

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With ethanol; hydrazine hydrate

: 127-06-0
acetone oxime

A: 75-31-0
isopropylamine

B: 108-18-9
diisopropylamine

Conditions

Conditions	Yield
With hydrogen; nickel at 180 - 200℃;

: 187737-37-7
propene

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With ammonia; sodium at 270℃; under 735508 Torr;
With ammonia; sodium at 250℃; under 661957 Torr;
With ammonia
With ammonia at 250℃; under 661957 Torr;

: 187737-37-7
propene

A: 75-31-0
isopropylamine

B: 108-18-9
diisopropylamine

Conditions

Conditions	Yield
With ammonia at 250℃; under 661957 Torr;

: 2973-10-6
diisopropyl sulfate

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With monoisopropyl sulfate; ammonia at 200 - 250℃; under 51485.6 - 88260.9 Torr;

: 2973-10-6
diisopropyl sulfate

A: 75-31-0
isopropylamine

B: 108-18-9
diisopropylamine

Conditions

Conditions	Yield
With monoisopropyl sulfate; ammonia at 200 - 250℃; under 120 - 51485.6 Torr;

: 563-83-7
ISOPROPYLAMIDE

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With potassium hydroxide; bromine

: 134252-16-7
1-hydroxy-2-propanone oxime

A: 6168-72-5
2-Amino-1-propanol

B: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With sodium amalgam; acetic acid

: 37110-18-2
1,3-dihydroxyacetone oxime

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With sodium amalgam; acetic acid

: 3964-18-9
2,3-dimethyl-2,3-dinitrobutane

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; diethyl ether

: 598-45-8
i-propyl isocyanide

: 75-31-0
isopropylamine

Conditions

Conditions	Yield
With hydrogenchloride

: 108-24-7
acetic anhydride

: 75-31-0
isopropylamine

: 1118-69-0
N-isopropylacetamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; Cooling with ice;	100%
With potassium carbonate; triethylamine In dichloromethane at 0 - 20℃; for 12h;	89.5%
With triethylamine In dichloromethane at 20℃; for 2h;	73%

: 100-52-7
benzaldehyde

: 75-31-0
isopropylamine

: 6852-56-8
N-benzylideneisopropylamine

Conditions

Conditions	Yield
at 20 - 100℃; for 0.133333h; microwave irradiation;	100%
at 20℃; for 2h;	100%
With magnesium sulfate In 1,2-dichloro-ethane at 60℃; for 18h; Glovebox;	85%

: 98-88-4
benzoyl chloride

: 75-31-0
isopropylamine

: 5440-69-7
N-isopropylbenzamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere;	100%
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere; Schlenk technique;	98%
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere; Schlenk technique;	98%

: 75-31-0
isopropylamine

: 98-59-9
p-toluenesulfonyl chloride

: 21230-07-9
N-isopropyl-p-toluenesulfonamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	100%
With pyridine; dmap In dichloromethane at 0 - 20℃; for 16h;	99%
With pyridine at 0 - 25℃; Inert atmosphere; Schlenk technique;	99%

: 75-31-0
isopropylamine

: 407-25-0
trifluoroacetic anhydride

: 348-76-5
2,2,2-trifluoro-N-(1-methylethyl)acetamide

Conditions

Conditions	Yield
With pyridine; dmap In tetrahydrofuran at 20℃; for 15h;	100%
With diethyl ether
In diethyl ether
at 0℃; than Rt, 3 h;
In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; Glovebox;

: 75-31-0
isopropylamine

: 140-88-5
ethyl acrylate

: 16217-22-4
3-isopropylaminopropionic acid ethyl ester

Conditions

Conditions	Yield
In tetrahydrofuran; ethanol at 0 - 20℃; for 16h;	100%
In ethanol at 0 - 20℃; for 24h;	100%
With poly(ethylene glycol) 2000; ruthenium trichloride at 50℃; for 8h; aza-Michael addition;	91%

: 75-31-0
isopropylamine

: 105-56-6
ethyl 2-cyanoacetate

: 52573-74-7
2-cyano-N-isopropylacetamide

Conditions

Conditions	Yield
for 18h;	100%
With sodium hydroxide

: 1177-35-1
2,4,6-Tris(4-methylphenoxy)-1,3,5-triazine

: 75-31-0
isopropylamine

: 79922-84-2
(4,6-Bis-p-tolyloxy-[1,3,5]triazin-2-yl)-isopropyl-amine

Conditions

Conditions	Yield
	100%

: 123-11-5
4-methoxy-benzaldehyde

: 75-31-0
isopropylamine

: 13033-52-8
N-(2-propyl)-4-methoxybenzylideneamine

Conditions

Conditions	Yield
In chloroform at 20℃; for 24h;	100%
at 20 - 100℃; for 0.133333h; microwave irradiation;	85%
at 20℃; for 48h;	83%

: 4637-24-5
N,N-dimethyl-formamide dimethyl acetal

: 75-31-0
isopropylamine

: 32150-24-6
N2-iso-propyl-N1,N1-dimethylformamidine

Conditions

Conditions	Yield
at 60℃;	100%

: 116-16-5
1,1,1,3,3,3-hexachloro-propan-2-one

: 75-31-0
isopropylamine

A: 67-66-3
chloroform

B: 23144-67-4
N-Isopropyl-2,2,2-trichloroacetamide

Conditions

Conditions	Yield
In hexane	A n/a B 100%

...Expand

: 623-43-8, 4358-59-2, 18707-60-3, 130981-57-6
methyl crotonate

: 75-31-0
isopropylamine

: 161722-25-4
methyl β-isopropylaminobutanoate

Conditions

Conditions	Yield
zirconium(IV) chloride In acetonitrile at 30℃; under 750.06 Torr; for 24h; Product distribution; var. α,β-unsat. ester, catalyst, pressure, temp.;	100%
zirconium(IV) chloride In acetonitrile at 30℃; under 750.06 Torr; for 24h;	100%
In acetone for 30h; Heating;

: 816-21-7
1,3-dibromo-pentan-2-one

: 75-31-0
isopropylamine

: 81981-83-1
Bis-(N-isopropyl)pentane-1,2-diimine

Conditions

Conditions	Yield
In pentane for 22h;	100%
With magnesium sulfate In pentane for 22h; Ambient temperature;	96%

: 1768-31-6
pentachloroacetone

: 75-31-0
isopropylamine

A: 67-66-3
chloroform

B: 39063-24-6
N-Isopropyl-2,2-dichloroacetamide

Conditions

Conditions	Yield
In hexane for 0.5h;	A n/a B 100%

...Expand

: 59938-06-6
(E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one

: 75-31-0
isopropylamine

: 127223-90-9
(Z)-1,1,1-Trifluoro-4-isopropylamino-but-3-en-2-one

Conditions

Conditions	Yield
In acetonitrile Ambient temperature;	100%

: 50777-76-9
(2-formylphenyl)(diphenyl)phosphine

: 75-31-0
isopropylamine

: isopropylamine

Conditions

Conditions	Yield
In methanol; dichloromethane at 20℃; for 2h; Inert atmosphere;	100%
In toluene at 150 - 160℃; for 6h; Inert atmosphere;	97%
In methanol; dichloromethane at 20℃; for 3h;	83%
for 4h; Heating;	80%

: 61249-00-1
(S)-(1-naphthyl) glycidyl ether

: 75-31-0
isopropylamine

: 4199-09-1
(S)-1-isopropylamino-3-(1-naphthyloxy)-2-propanol

Conditions

Conditions	Yield
In water for 3h; Heating;	100%
In water for 1h; Heating;	99%
With Na-zeolite In acetonitrile at 20℃; for 12h;	95%

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

: 75-31-0
isopropylamine

: 115975-38-7
2,2,2-Trifluoro-1-[4-isopropylamino-3-(2,2,2-trifluoro-acetyl)-naphthalen-1-yl]-ethanone

Conditions

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

: 128336-73-2
N-ethoxycarbonylaminomethylphosphonic acid

: 75-31-0
isopropylamine

: 128336-79-8
(Ethoxycarbonylamino-methyl)-phosphonic acid; compound with isopropylamine

Conditions

Conditions	Yield
In ethanol	100%

: 53583-75-8
N-(triethylstannyl)succinimide

: 75-31-0
isopropylamine

: 3026-11-7
N-isopropylsuccinamide

Conditions

Conditions	Yield
In methanol at 90℃; for 2h;	100%

: 105116-44-7
N-Boc-cyclohexylnorstatin

: 75-31-0
isopropylamine

: 119600-98-5
Boc-cyclohexylnorstatine isopropylamide

Conditions

Conditions	Yield
With N-hydroxy-5-norbornene-2,3-dicarboximide; dicyclohexyl-carbodiimide In ethyl acetate Ambient temperature;	100%

: 104429-28-9
N-Isopropyl-N-((1E,3E)-6,6,6-trifluoro-5-oxo-hexa-1,3-dienyl)-acetamide

: 75-31-0
isopropylamine

: 132630-54-7
(3E,5E)-1,1,1-Trifluoro-6-isopropylamino-hexa-3,5-dien-2-one

Conditions

Conditions	Yield
In acetonitrile for 4h; Ambient temperature;	100%

: 82912-51-4
2-m-chlorobenzoyloxy-4-isopropyl-2H-1,4-thiazin-3-one

: 75-31-0
isopropylamine

: 85331-45-9
4-Isopropyl-2-isopropylamino-4H-[1,4]thiazin-3-one

Conditions

Conditions	Yield
for 24h; Ambient temperature;	100%

: 75-31-0
isopropylamine

: 132005-35-7
(S)-(+)-1-chloro-3-(1-naphthyloxy)-2-propanol

: 318-98-9, 3506-09-0, 4199-10-4, 13071-11-9
(R)-propranolol hydrochloride

Conditions

Conditions	Yield
With sodium hydroxide; water for 16h; Ambient temperature;	100%

: 108508-19-6
(R)-(-)-1-chloro-2-acetoxy-3-(1-naphthyloxy)propane

: 75-31-0
isopropylamine

: 4199-10-4
(S)-(-)-propanolol hydrochloride

Conditions

Conditions	Yield
With sodium hydroxide; water for 16h; Ambient temperature;	100%

: 125103-12-0
2-Chloro-3-<α-cyano-α-(benzimidazol-2-yl)methylene>3,4-dihydroquinoxaline

: 75-31-0
isopropylamine

: 120340-83-2
1-Isopropyl-2-Amino-3-(benzimidazol-2-yl)pyrrolo<2,3-b>quinoxaline

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 130℃; for 4h; sealed ampul;	100%

: 142386-32-1, 142435-86-7
(+/-)-threo 2,3-epoxy-1-phenylphospholane 1-oxide

: 75-31-0
isopropylamine

: 142386-34-3
(1S,2R,3R)-2-Isopropylamino-1-oxo-1-phenyl-1λ5-phospholan-3-ol

Conditions

Conditions	Yield
In methanol at 40℃; Ring cleavage; addition;	100%
at 40℃; for 48h;

: 90162-90-6
1-(octylthio)carbonyl-3-(tetrahydrofuryl)-5-fluorouracil

: 75-31-0
isopropylamine

: 63901-83-7
5-fluoro-3-(tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

Conditions

Conditions	Yield
In diethyl ether for 0.166667h; Ambient temperature;	100%

: 81102-68-3
Toluene-4-sulfonic acid (S)-2-hydroxy-3-(2-methyl-3-nitro-phenoxy)-propyl ester

: 75-31-0
isopropylamine

: 81132-32-3
<2R>-(+)-1-isopropylamino-3-(2-methyl-3-nitrophenoxy)-2-propanol

Conditions

Conditions	Yield
In toluene for 10h; Heating;	100%

: 132630-60-5
1-ethylthio-4,4-bis(trifluoroacetyl)-1,3-butadiene

: 75-31-0
isopropylamine

: 3-trifluoroacetyl-2-trifluoromethyl-2-hydroxy-1-isopropyl-1,2-dihydropyridine

Conditions

Conditions	Yield
In acetonitrile for 1h; Ambient temperature;	100%

Isopropylamine Chemical Properties

Structure of Isopropylamine (CAS NO.75-31-0):

IUPAC Name: propan-2-amine
Empirical Formula: C₃H₉N
Molecular Weight: 59.1103
Index of Refraction: 1.389
Molar Refractivity: 19.44 cm³
Molar Volume: 82.1 cm³
Polarizability: 7.7×10^-24cm³
Surface Tension: 22 dyne/cm
Density: 0.719 g/cm³
Enthalpy of Vaporization: 27.83 kJ/mol
Melting Point: -101 °C
Boiling Point: 30.9 °C at 760 mmHg
Vapour Pressure: 608 mmHg at 25°C
storage temp: 2-8°C
Water Solubility: soluble
Sensitive: Air Sensitive
Physical Appearance: colourless liquid
Stability: Stable. Extremely flammable - note low boiling point and low flash point. Readily forms explosive mixtures with air. Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides, perchloryl fluoride.

Isopropylamine Uses

Isopropylamine (CAS NO.75-31-0) is an organic compound, an amine.The main uses of isopropylamine are as the salt component to Glyphosate acid for weed prevention .

Isopropylamine Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
guinea pig	LD50	oral	2700mg/kg (2700mg/kg)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 45(3), Pg. 79, 1980.
mammal (species unspecified)	LC50	inhalation	1800mg/m3 (1800mg/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	500mg/kg (500mg/kg)		Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 14, Pg. 80, 1975.
mouse	LCLo	inhalation	7000ppm/40M (7000ppm)		Shell Chemical Company. Unpublished Report. Vol. -, Pg. 7, 1961.
mouse	LD50	oral	2200mg/kg (2200mg/kg)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 45(3), Pg. 79, 1980.
rabbit	LD50	oral	3200mg/kg (3200mg/kg)	GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA" SKIN AND APPENDAGES (SKIN): HAIR: OTHER	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 45(3), Pg. 79, 1980.
rabbit	LD50	skin	380mg/kg (380mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rat	LC50	inhalation	4000ppm/4H (4000ppm)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rat	LD50	oral	111mg/kg (111mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA GASTROINTESTINAL: OTHER CHANGES	National Technical Information Service. Vol. OTS0542011,
rat	LDLo	intraperitoneal	50mg/kg (50mg/kg)		Farmakologiya i Toksikologiya Vol. 31, Pg. 238, 1968.

Isopropylamine Consensus Reports

Isopropylamine (CAS NO.75-31-0) can be obtained by aminating isopropyl alcohol with ammonia in presence of a nickel/copper or similar catalyst:

(CH₃)₂CHOH + NH₃ → (CH₃)₂CHNH₂ + H₂O

Isopropylamine Safety Profile

Hazard Codes: Highly F+, Irritant Xi
Risk Statements: 12-36/37/38
R12:Extremely flammable.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 16-26-29
S16:Keep away from sources of ignition.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S29:Do not empty into drains.
RIDADR: UN 1221 3/PG 1
WGK Germany: 1
RTECS: NT8400000
F: 34
HazardClass: 3
PackingGroup: I

Isopropylamine Specification

Isopropylamine , its cas register number is 75-31-0. It also can be called 1-Methylethylamine ; 2-Amino-propaan ; 2-Amino-propano ; 2-Aminopropan ; 2-Aminopropane ; Isopropilamina ; Isopropylamine ; Monoisopropylamine ; Propanal, 2-amino- ; Propane, 2-amino- ; sec-Propylamine .

Product Name

Isopropylamine

Synthetic route

Isopropylamine Chemical Properties

Isopropylamine Uses

Isopropylamine Toxicity Data With Reference

Isopropylamine Consensus Reports

Isopropylamine Safety Profile

Isopropylamine Specification

Related Products

Hot Products