4-IsopropylAniline supplier

Name
4-Isopropylaniline
EINECS 202-797-2
CAS No. 99-88-7
Article Data63
CAS DataBase
Density 0.989
Solubility insoluble
Melting Point -63 ºC
Formula C9H13 N
Boiling Point 226-228 ºC
Molecular Weight 135.209
Flash Point 92 ºC
Transport Information
Appearance light brown clear liquid
Safety S36/37
Risk Codes R20/21/22
Molecular Structure
Hazard Symbols
Synonyms Cumidine(6CI,7CI,8CI); 1-Amino-4-isopropylbenzene; 4-(1-Methylethyl)benzenamine;4-(2-Propyl)aniline; 4-Amino-1-isopropylbenzene; 4-Aminocumene;4-Aminoisopropylbenzene; 4-Isopropylaniline; 4-Isopropylbenzenamine;4-Isopropylphenylamine; NSC 7198; [4-(1-Methylethyl)phenyl]amine; p-Cumidine;p-Isopropylaniline; b-(4-Aminophenyl)propane
PSA 26.02000
LogP 2.97340

Synthetic route

: 1817-47-6
4-nitrocumene

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With triethylamine In water at 80℃; for 2h; Inert atmosphere; Green chemistry; chemoselective reaction;	99%
With borane-ammonia complex In methanol; water at 49.84℃; for 0.1h; Catalytic behavior;	99%
With nickel; ammonium chloride In water at 80 - 90℃; for 1.5h;	96%

: 16152-51-5
(4-isopropylphenyl)boronic acid

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With copper(I) oxide; ammonium hydroxide; air In methanol at 20℃; for 12h;	88%

: 15887-26-0
1,2-Bis(4-isopropylphenyl)diazene

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With perchloric acid In isopropyl alcohol; acetonitrile at 25℃; for 0.8h; pH=2; Inert atmosphere; Irradiation;	88%

: 920-39-8
isopropylmagnesium bromide

: 540-37-4
p-aminoiodobenzene

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride In tetrahydrofuran -78 deg C, 10 min, reflux, 24 h;	87%

: 768-52-5
N-Isopropylaniline

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With aluminum oxide; aluminium trichloride for 0.0583333h; microwave irradiation;	87%

: 586-61-8
2-(4-bromophenyl)propane

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With ammonium hydroxide; L-2-O-methyl-chiro-inositol; copper(II) acetate monohydrate In 1-methyl-pyrrolidin-2-one at 110℃; for 20h;	87%

: 2621-46-7
1-chloro-4-isopropylbenzene

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With ammonium sulfate; bis(1,5-cyclooctadiene)nickel (0); sodium t-butanolate at 100 - 110℃; for 12h;	81%

: 63693-65-2
4-isopropylphenylhydrazine

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20℃; Reduction;	72%

: 98-82-8
Isopropylbenzene

A: 99-88-7
4-Isopropylaniline

B: 5369-16-4
meta-iso-propyl aniline

C: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
With tris-(2-chloro-ethyl)-amine; trifluorormethanesulfonic acid; trifluoroacetic acid In chloroform at 25℃; for 5h;	A 37% B 9% C 48%

...Expand

: 62-53-3
aniline

: 67-63-0
isopropyl alcohol

A: 187737-37-7
propene

B: 99-88-7
4-Isopropylaniline

C: 768-52-5
N-Isopropylaniline

D: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
With Ce-Y zeolite at 300℃; Product distribution; var. zeolites, temp., and flow rate;	A n/a B 1.9% C 4% D 10.7%

...Expand

: 98-82-8
Isopropylbenzene

A: 99-88-7
4-Isopropylaniline

B: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
With nitric acid man faellt mit Wasser das rohe Nitrocumol als Oel aus und reduziert es mit Schwefelammon in alkoh. Loesung;
With sulfuric acid; nitric acid man faellt mit Wasser das rohe Nitrocumol als Oel aus und reduziert es mit Zink und Salzsaeure;
Stage #1: Isopropylbenzene With nitric acid at 10℃; for 0.166667h; Flow reactor; Stage #2: In toluene at 100℃; under 30003 Torr; Flow reactor; Overall yield = 76.79 %Chromat.;	A 59.4 %Chromat. B 16.7 %Chromat.

: 768-52-5
N-Isopropylaniline

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
With cobalt(II) chloride at 250℃;
With zinc dibromide at 250℃;
With cadmium(II) chloride at 250℃;

: 2479-47-2
4,4'-(1-methyl-ethane-1,1-diyl)-bis-aniline

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
With nickel at 200℃; under 36775.4 Torr; Hydrogenation;
With nickel; cyclohexanol at 200℃;

: 62-53-3
aniline

: 67-63-0
isopropyl alcohol

A: 99-88-7
4-Isopropylaniline

B: N,4-diisopropylaniline

Conditions

Conditions	Yield
With zinc(II) chloride at 260℃;

...Expand

: 74-98-6
propane

: 62-53-3
aniline

A: 99-88-7
4-Isopropylaniline

B: 5369-16-4
meta-iso-propyl aniline

C: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
With oxygen In gaseous matrix at 80℃; Irradiation;	A 35 % Spectr. B 2 % Spectr. C 63 % Spectr.
With oxygen In gaseous matrix at 80℃; Irradiation;	A 35 % Spectr. B n/a C n/a

...Expand

: 74-98-6
propane

: 62-53-3
aniline

A: 99-88-7
4-Isopropylaniline

B: 5369-16-4
meta-iso-propyl aniline

C: 768-52-5
N-Isopropylaniline

D: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
at 40℃; Mechanism; Product distribution; Irradiation; intramolecular selectivity in the gas-phase alkylation and acetylation of aniline by charged electrophiles;

...Expand

: 2479-47-2
4,4'-(1-methyl-ethane-1,1-diyl)-bis-aniline

nickel: nickel

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
at 200℃; under 36775.4 Torr; Hydrogenation;

...Expand

: 2479-47-2
4,4'-(1-methyl-ethane-1,1-diyl)-bis-aniline

: 108-93-0
cyclohexanol

nickel: nickel

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
at 225℃;

...Expand

4-nitro-cumene: 4-nitro-cumene

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With nickel; isopropyl alcohol at 100℃; under 58840.6 Torr; Hydrogenation;
With hydrogenchloride; tin
With hydrogenchloride; iron

: 768-52-5
N-Isopropylaniline

cadmium chloride: cadmium chloride

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
at 250℃;

...Expand

: 768-52-5
N-Isopropylaniline

cobalt (II)-chloride: cobalt (II)-chloride

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
at 250℃;

...Expand

: 768-52-5
N-Isopropylaniline

zinc bromide: zinc bromide

A: 99-88-7
4-Isopropylaniline

B: 62-53-3
aniline

Conditions

Conditions	Yield
at 250℃;

...Expand

: 7647-01-0
hydrogenchloride

: 100990-57-6
N-(4-iso-propylphenyl)benzamide

A: 99-88-7
4-Isopropylaniline

B: 65-85-0
benzoic acid

Conditions

Conditions	Yield
at 150℃;

...Expand

: 768-52-5
N-Isopropylaniline

A: 187737-37-7
propene

B: 99-88-7
4-Isopropylaniline

C: 62-53-3
aniline

D: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
Ce-Y zeolite In hexane at 30℃; Product distribution; Further Variations:; Catalysts; Temperatures; other alkyl aniline; Isomerization; dealkylation;

...Expand

: 34123-59-6
N-(4-isopropylphenyl)-N',N'-dimethylurea

A: 99-88-7
4-Isopropylaniline

B: 124-40-3
dimethyl amine

Conditions

Conditions	Yield
With sulfuric acid In methanol; water at 80 - 90℃; Kinetics; Further Variations:; Temperatures;

: 34123-59-6
N-(4-isopropylphenyl)-N',N'-dimethylurea

A: 7260-94-8
N,N-dimethylcarbamic acid

B: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With sodium hydroxide In methanol; water at 90℃; Kinetics; Further Variations:; Temperatures; pH-values;

: 34123-59-6
N-(4-isopropylphenyl)-N',N'-dimethylurea

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
With Arthrobacter sp. N2 In various solvent(s) pH=6.6; Kinetics;

: 62-53-3
aniline

: 67-63-0
isopropyl alcohol

A: 99-88-7
4-Isopropylaniline

B: 768-52-5
N-Isopropylaniline

C: 643-28-7
2-isopropylaniline

Conditions

Conditions	Yield
Li-Y zeolite at 350℃; Product distribution; Further Variations:; Catalysts; Temperatures;

...Expand

: 98-82-8
Isopropylbenzene

Raney nickel: Raney nickel

: 99-88-7
4-Isopropylaniline

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: aq. HNO3, H2SO4 / nitromethane 2: H2 / PtO2 / ethanol View Scheme

: 99-88-7
4-Isopropylaniline

: 108-24-7
acetic anhydride

: 5702-74-9
N-(4-iso-propylphenyl)acetamide

Conditions

Conditions	Yield
In dichloromethane at 20℃; Inert atmosphere;	100%
With ZnAl2O4 nanoparticles at 20℃; for 0.05h; Neat (no solvent);	96%
In neat (no solvent) at 20℃; for 0.05h;	96%

: 51673-84-8
dimethoxyacetaldehyde

: 99-88-7
4-Isopropylaniline

: 205192-94-5
N-[(2,2-dimethoxyethyl)amino]-4-(2-propyl)aniline

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In ethanol under 760 Torr; for 18h;	100%

: 99-88-7
4-Isopropylaniline

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 64321-60-4
diethyl 4-i-propylanilinomethylenemalonate

Conditions

Conditions	Yield
at 130℃; for 2h;	100%
at 120℃; for 4h; Inert atmosphere;

: 31739-56-7
2-(1H-pyrrol-1-yl)benzaldehyde

: 99-88-7
4-Isopropylaniline

: N-[4-(1-methylethyl)phenyl]-(2-(pyrrol-1-yl)phenylmethylen)amine

Conditions

Conditions	Yield
at 20℃;	100%

: 99-88-7
4-Isopropylaniline

: 1198592-03-8
[(2-{6-[(methyloxy)carbonyl]-3-phenyl-1H-indol-1-yl}ethyl)oxy]acetic acid

: 1198592-04-9
methyl 1-{2-[(2-{[4-(1-methylethyl)phenyl]amino}-2-oxoethyl)oxy]ethyl}-3-phenyl-1H-indole-6-carboxylate

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 16h;	100%

: 99-88-7
4-Isopropylaniline

: 50978-45-5
3-oxobenzo[d]isothiazole-2(3H)-carbaldehyde 1,1-dioxide

: 5279-58-3
N-[4-(propan-2-yl)phenyl]formamide

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 0.25h; chemoselective reaction;	100%

: 850424-11-2
2-chloro-6-methoxyquinazoline

: 99-88-7
4-Isopropylaniline

: 1374336-64-7
N-(4-isopropylphenyl)-6-methoxyquinazolin-2-amine

Conditions

Conditions	Yield
In ethanol at 80℃; for 16h;	100%

: 99-88-7
4-Isopropylaniline

: 160893-07-2
2-chloro-5-methoxyquinoline

: N-(4-isopropylphenyl)-5-methoxyquinolin-2-amine

Conditions

Conditions	Yield
In neat (no solvent) at 160℃;	100%
In neat (no solvent) at 160℃;

: 99-88-7
4-Isopropylaniline

: 73183-34-3
bis(pinacol)diborane

: 16152-51-5
(4-isopropylphenyl)boronic acid

Conditions

Conditions	Yield
With tert.-butylnitrite In acetonitrile at 0 - 80℃; for 2h;	99.8%
With tert.-butylnitrite In acetonitrile at 0 - 80℃; for 2h;	99.8%

: 64-18-6
formic acid

: 99-88-7
4-Isopropylaniline

: 5279-58-3
N-[4-(propan-2-yl)phenyl]formamide

Conditions

Conditions	Yield
for 16h; Reflux;	99%
With choline chloride*2SnCl2 at 70℃; for 0.333333h;	97%
With choline chloride*2SnCl2 at 70℃;	97%

: 99-88-7
4-Isopropylaniline

: 3282-30-2
pivaloyl chloride

: 448250-70-2
N-(4-isopropylphenyl)pivalamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	99%
With TEA In dichloromethane at 0 - 25℃; for 3h; Acylation;
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Trimethylacetic acid In dichloromethane at 20℃; for 18h;

: 99-88-7
4-Isopropylaniline

: 538-75-0
dicyclohexyl-carbodiimide

: N-(p-isopropylphenyl)-N',N''-dicyclohexylguanidine

Conditions

Conditions	Yield
[(Me3Si)2N]3Yb(μ-Cl)Li(THF)3 In dichloromethane at 40℃; for 4h;	99%
With C23H40AlN In toluene at 25℃; for 1h; Inert atmosphere; Schlenk technique;	92%
With [Cp2(Me)Zr(μ-O)Zr(NMe2)2(μ-O)Zr(Me)Cp2] In benzene-d6 at 110℃; for 12h; Temperature; Reagent/catalyst; Time; Inert atmosphere;

: 696-59-3
cis,trans-2,5-dimethoxytetrahydrofuran

: 99-88-7
4-Isopropylaniline

: 166963-93-5
1-(4-(iso-propyl)phenyl)-1H-pyrrole

Conditions

Conditions	Yield
In acetic acid; ethyl acetate	99%
In acetic acid; ethyl acetate	99%
In acetic acid for 1.5h; Heating / reflux;	99%

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 99-88-7
4-Isopropylaniline

: 884600-73-1
(4-isopropylphenyl){(E)-[4-(trifluoromethyl)phenyl]methylene}amine

Conditions

Conditions	Yield
Stage #1: 4-Trifluoromethylbenzaldehyde; 4-Isopropylaniline In water at 20℃; for 2h; Stage #2: In dichloromethane; water for 0.333333h;	99%

: 99-88-7
4-Isopropylaniline

: 609-67-6
2-Iodobenzoyl chloride

: 331270-10-1
2-iodo-N-(4-isopropylphenyl)benzamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 3h;	99%
With triethylamine In dichloromethane
With pyridine In dichloromethane at 0 - 20℃;

: 623-73-4
diazoacetic acid ethyl ester

: 99-88-7
4-Isopropylaniline

: 890169-52-5
ethyl 2-((4-isopropylphenyl)amino)acetate

Conditions

Conditions	Yield
With sodium dithionite; myoglobin mutant H64V,V68A In aq. phosphate buffer pH=8.0; Reagent/catalyst; chemoselective reaction;	99%
With sodium dithionite; Bacillus megaterium cytochrome P450 variant H2-5-F10 In aq. phosphate buffer at 20℃; for 12h; pH=8; Enzymatic reaction;	59%

: 99-88-7
4-Isopropylaniline

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

: C17H16N2O

Conditions

Conditions	Yield
In methanol Reflux;	99%

: 99-88-7
4-Isopropylaniline

: 100-51-6
benzyl alcohol

: N-benzyl-4-isopropylaniline

Conditions

Conditions	Yield
With C55H43ClN5P2Ru(1+)*Cl(1-); potassium hydroxide In toluene at 140℃; for 2h; Sealed tube;	99%
With C17H18IrN3O; caesium carbonate at 120℃; for 20h; Inert atmosphere;	93%
With tetrakis[3,5-bis(trifluoromethyl)phenyl]boric acid bis(diethyl ether) complex; C32H63CoNP2Si(2+) In toluene for 48h; Molecular sieve; Reflux; Inert atmosphere; chemoselective reaction;	90%
With 9-N-methylamino-1-oxophenalene; potassium tert-butylate In toluene at 130℃; for 18h; Inert atmosphere;	81%
With [(NH-C3H5)Tr(NHP(iPr)2)2CoCl2]; potassium tert-butylate In toluene at 80℃; for 24h;	76%

: 590-28-3
potassium cyanate

: 99-88-7
4-Isopropylaniline

: 56046-17-4
3-[4-(1-methylethyl)]phenylurea

Conditions

Conditions	Yield
With hydrogenchloride In water at 20℃; for 2h; Inert atmosphere;	99%

: 2406-05-5
3-bromo-3-methyl-2-indolinone

: 99-88-7
4-Isopropylaniline

: (R)-3-((4-isopropylphenyl)amino)-3-methylindolin-2-one

Conditions

Conditions	Yield
Stage #1: 3-bromo-3-methyl-2-indolinone With nickel(II) tetrafluoroborate hexahydrate; C42H66N4O8 In ethyl acetate at 35℃; for 0.583333h; Stage #2: With N-ethyl-N,N-diisopropylamine In ethyl acetate at 0℃; for 0.166667h; Stage #3: 4-Isopropylaniline In ethyl acetate at 0℃; for 24h; enantioselective reaction;	99%

: 2417-73-4
methyl 2-bromomethylbenzoate

: 99-88-7
4-Isopropylaniline

: 2-(4-isopropylphenyl)isoindolin-1-one

Conditions

Conditions	Yield
at 140℃; for 2h;	98.35%

: 32315-10-9
bis(trichloromethyl) carbonate

: 99-88-7
4-Isopropylaniline

: 31027-31-3
4-isopropylphenylisocyanate

Conditions

Conditions	Yield
In 1,2-dichloro-ethane at 70 - 83℃;	98.2%
With triethylamine In benzene Substitution; dehydrochlorination; Heating;	66.2%
With triethylamine In dichloromethane at 0 - 20℃; for 0.0833333h;

: 99-88-7
4-Isopropylaniline

: 122-01-0
4-chloro-benzoyl chloride

: 4-Chloro-N-(4-isopropyl-phenyl)-benzamide

Conditions

Conditions	Yield
With pyridine for 24h; Ambient temperature;	98%

: 24424-99-5
di-tert-butyl dicarbonate

: 99-88-7
4-Isopropylaniline

: 164226-14-6
4-isopropyl-N-tert-butoxycarbonylaniline

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 25℃; for 17h; Inert atmosphere;	98%
With choline chloride; urea at 50℃; Green chemistry;	95%
With 3a,6a-diphenylglycoluril In ethanol at 25 - 30℃; for 0.333333h; Catalytic behavior; Reagent/catalyst;	95%
With triethylamine In tetrahydrofuran at 25℃; for 17h; Inert atmosphere;	67%
With dmap In dichloromethane at 20℃; for 0.5h;

: 99-88-7
4-Isopropylaniline

: 1-azido-4-isopropylbenzene

Conditions

Conditions	Yield
Stage #1: 4-Isopropylaniline With hydrogenchloride; sodium nitrite In water; ethyl acetate at 0℃; for 1h; Stage #2: With sodium azide In water; ethyl acetate at 20℃; for 4h;	98%
With tert.-butylnitrite; trimethylsilylazide In acetonitrile at 20℃; for 1h;	96%
Stage #1: 4-Isopropylaniline With hydrogenchloride; sodium nitrite In water at 0℃; for 2h; Stage #2: With sodium azide In water at 0 - 20℃;	94%

: 99-88-7
4-Isopropylaniline

: 693-13-0
diisopropyl-carbodiimide

: N-(p-isopropylphenyl)-N',N''-diisopropylguanidine

Conditions

Conditions	Yield
[(Me3Si)2N]3Yb(μ-Cl)Li(THF)3 In tetrahydrofuran at 60℃; for 4h;	98%
With C23H40AlN In toluene at 25℃; for 1h; Inert atmosphere; Schlenk technique;	89%

: 99-88-7
4-Isopropylaniline

: 16616-42-5
p-chlorobenzoylphenylacetylene

: 1025784-68-2
(Z)-3-(4-isopropylphenylamino)-1-(4-chlorophenyl)-3-phenylprop-2-en-1-one

Conditions

Conditions	Yield
at 80℃; for 1h; Michael addition;	98%

: 99-88-7
4-Isopropylaniline

: 79-44-7
N,N-Dimethylcarbamoyl chloride

: 34123-59-6
N-(4-isopropylphenyl)-N',N'-dimethylurea

Conditions

Conditions	Yield
With sodium carbonate; sodium iodide In hexane at 50℃; for 16h; pH=7;	98%
With triethylamine In dichloromethane at 0 - 20℃; for 24h;

: 99-88-7
4-Isopropylaniline

: 643-79-8
o-phthalic dicarboxaldehyde

: 1093076-04-0
1-p-isopropylphenylimino-2-p-isopropylphenylisoindoline

Conditions

Conditions	Yield
With formic acid In diethyl ether at 20℃; for 12h; Inert atmosphere;	98%

4-IsopropylAniline Chemical Properties

Product Name:4-Isopropylaniline.
The MF of 4-Isopropylaniline(99-88-7) is C₉H₁₃N.

The MW of 4-Isopropylaniline(99-88-7) is 135.21.
Synonyms:4-AMINO-1-ISOPROPYLBENZENE;4-AMINOCUMENE;4-AMINOCUMOL;4-ISOPROPYLANILINE;AKOS BBS-00003562;CUMIDENE;CUMIDINE;P-ISOPROPYLANILINE
EINECS: 202-797-2
Mol File: 99-88-7.mol
MP:-63 °C
FP:198 °F
BP:226-227 °C745 mm Hg(lit.)
Density:0.989 g/mL at 25 °C(lit.)
Refractive index:n20/D 1.543(lit.)
Water Solubility:insoluble
Sensitive:Light Sensitive
Merck:14,2620
BRN:1930544
CAS DataBase Reference:99-88-7(CAS DataBase Reference)
NIST Chemistry Reference:99-88-7(NIST)

4-IsopropylAniline Uses

The 4-Isopropylaniline(99-88-7) is used as an intermediate herbicide isoproturon,medicine and pesticide intermediates.

4-IsopropylAniline Toxicity Data With Reference

RTECS#: CAS# 99-88-7: None listed
LD50/LC50: RTECS: Not available.
Carcinogenicity: 4-Isopropylaniline - Not listed as a carcinogen by ACGIH, IARC, NTP, or CA Prop 65.
Other: The toxicological properties have not been fully investigated.

4-IsopropylAniline Safety Profile

Safety information of 4-Isopropylaniline(99-88-7):
Hazard Codes:

Xi,Xn
Risk Statements:36/37/38-20/21/22
R36/37/38:Irritating to eyes, respiratory system and skin ;
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed ;
Safety Statements:26-36/37
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice ;
S36/37:Wear suitable protective clothing and gloves ;
WGK Germany:2
Hazard Note:Irritant
HS Code:29214980

4-IsopropylAniline Specification

It is air sensitive and light sensitive.Incompatibilities with strong oxidizing agents, strong acids.Hazardous decomposition products are carbon monoxide, oxides of nitrogen, carbon dioxide.

Product Name

4-Isopropylaniline

Synthetic route

4-IsopropylAniline Chemical Properties

4-IsopropylAniline Uses

4-IsopropylAniline Toxicity Data With Reference

4-IsopropylAniline Safety Profile

4-IsopropylAniline Specification

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