4-methyl-2-pentanone
N-phenylphenylene-1,4-diamine
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
With hydrogen at 99.84℃; under 18751.9 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Time; Autoclave; | 100% |
With hydrogen; pyrographite at 20 - 150℃; under 22052.2 Torr; for 0.1h; Autoclave; | 99.4% |
With platinum on activated charcoal; isopropyl alcohol at 50 - 150℃; under 36775.4 Torr; Hydrogenation; |
C18H22N2
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In 5,5-dimethyl-1,3-cyclohexadiene at 100℃; under 7500.75 Torr; Solvent; Temperature; | 92.6% |
p-nitrosodiphenylamine
4-methyl-2-pentanone
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
With platinum on activated charcoal; isopropyl alcohol at 50 - 150℃; under 25742.8 Torr; Hydrogenation; |
4-ntrophenyl(phenyl)amine
4-methyl-2-pentanone
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
With platinum on activated charcoal; isopropyl alcohol at 50 - 150℃; under 25742.8 Torr; Hydrogenation; |
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
With formic acid; palladium on activated charcoal at 85℃; Yield given; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 5percent Pd/C 2: 5percent palladium-on-carbon / 85 °C 3: HCOOH / 5percent Pd/C / 85 °C View Scheme | |
Multi-step reaction with 3 steps 1: formic acid / 5percent Pd/C / 85 °C 2: 5percent palladium-on-carbon / 85 °C 3: HCOOH / 5percent Pd/C / 85 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 5percent palladium-on-carbon / 85 °C 2: HCOOH / 5percent Pd/C / 85 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 5percent palladium-on-carbon / 85 °C 2: HCOOH / 5percent Pd/C / 85 °C View Scheme |
2-amino-4-methylpentane
4-(phenylimino)cyclohexa-2,5-dienone
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
In methanol |
4-methyl-2-pentanone
N-phenylphenylene-1,4-diamine
A
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
B
C18H22N2
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen at 200℃; under 30003 Torr; Reagent/catalyst; | |
With hydrogen at 160℃; under 22502.3 Torr; for 4h; Autoclave; |
4-methyl-2-pentanone
N-phenylphenylene-1,4-diamine
A
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
B
aniline
Conditions | Yield |
---|---|
With 10% Pd/C; hydrogen at 160℃; under 22502.3 Torr; for 4h; Autoclave; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogen 2: pyrographite; ; hydrogen / 0.1 h / 20 - 150 °C / 22052.2 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sulfuric acid; nitric acid / chloroform; benzene / 5 h / 50 °C / Industrial scale 2: tetramethyl ammoniumhydroxide; platinum on carbon; hydrogen / water / 80 °C / 11251.1 Torr 3: pyrographite; ; hydrogen / 0.1 h / 20 - 150 °C / 22052.2 Torr / Autoclave View Scheme | |
Multi-step reaction with 4 steps 1: sulfuric acid; nitric acid / chloroform; benzene / 5 h / 50 °C / Industrial scale 2: hydrogen / 200 °C / Industrial scale 3: tetramethyl ammoniumhydroxide; platinum on carbon; hydrogen / water / 80 °C / 11251.1 Torr 4: pyrographite; ; hydrogen / 0.1 h / 20 - 150 °C / 22052.2 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: ammonia / 450 °C / 760.05 Torr / Industrial scale 2: tetramethyl ammoniumhydroxide; platinum on carbon; hydrogen / water / 80 °C / 11251.1 Torr 3: pyrographite; ; hydrogen / 0.1 h / 20 - 150 °C / 22052.2 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: hydrogen / 200 °C / Industrial scale 2: tetramethyl ammoniumhydroxide; platinum on carbon; hydrogen / water / 80 °C / 11251.1 Torr 3: pyrographite; ; hydrogen / 0.1 h / 20 - 150 °C / 22052.2 Torr / Autoclave View Scheme | |
Multi-step reaction with 3 steps 1: tetramethyl ammoniumhydroxide / water / 2.1 h / 75 °C / 55 Torr / Dean-Stark 2: hydrogen; 5%-palladium/activated carbon / 0.5 h / 80 °C / 11251.1 Torr / Autoclave 3: 3 % platinum on carbon; hydrogen / 0.5 h / 155 °C / 26252.6 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tetramethyl ammoniumhydroxide / water / 2.1 h / 75 °C / 55 Torr / Dean-Stark 2: hydrogen; 5%-palladium/activated carbon / 0.5 h / 80 °C / 11251.1 Torr / Autoclave 3: 3 % platinum on carbon; hydrogen / 0.5 h / 155 °C / 26252.6 Torr / Autoclave View Scheme |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 20℃; for 48h; Cooling with ice; | 86% |
Conditions | Yield |
---|---|
Stage #1: N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine With magnesium sulfate; silver(l) oxide In toluene at 25℃; for 15h; Stage #2: prop-2-ene-1-thiol In ethanol at 25℃; | 65% |
ethene
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
A
C22H32N2
C
C24H36N2
Conditions | Yield |
---|---|
diethylaluminium chloride In hexane for 12 - 16h; Product distribution / selectivity; | A 47.2% B n/a C n/a |
Conditions | Yield |
---|---|
Stage #1: Adipic acid With thionyl chloride; N,N-dimethyl-formamide In tetrahydrofuran; chloroform for 8h; Reflux; Stage #2: N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine With pyridine In tetrahydrofuran at 20℃; Cooling with ice; | 39% |
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: Ag2O; MgSO4 / toluene / 15 h / 25 °C 1.2: 65 percent / ethanol / 25 °C 2.1: 75 percent / 150 - 155 °C View Scheme |
thiophosgene
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
potassium carbonate
N-(4-anilinophenyl)-N-(1,3-dimethyl-butyl)-thiocarbamate-O-methyl ester
Conditions | Yield |
---|---|
In methanol; chloroform |
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
methyl iodide
N-(4-anilinophenyl)-N-(1,3-dimethyl-butyl)-dithiocarbamate methyl ester
Conditions | Yield |
---|---|
With carbon disulfide; sodium hydroxide In tetrahydrofuran |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; aluminum (III) chloride at 160 - 170℃; for 27h; Friedel Crafts Alkylation; |
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
4-hydroxy-3,5-di-tert-butylphenylpropionic acid
Conditions | Yield |
---|---|
With boric acid In toluene for 15h; Dean-Stark; Inert atmosphere; Reflux; |
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
methyl 3-(4-hydroxy-3,5-di-tert-butyl)phenylpropanoate
Conditions | Yield |
---|---|
With boric acid In toluene for 15h; Dean-Stark; Inert atmosphere; Reflux; Molecular sieve; |
1,3,5-trichloro-2,4,6-triazine
4-(3-hydroxypropyl)-2,6-di-tert-butylphenol
N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine
Conditions | Yield |
---|---|
Stage #1: 1,3,5-trichloro-2,4,6-triazine; 4-(3-hydroxypropyl)-2,6-di-tert-butylphenol With triethylamine In tetrahydrofuran at 0℃; for 4h; Inert atmosphere; Stage #2: N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine In tetrahydrofuran at 65℃; for 15h; Inert atmosphere; |
IUPAC Name: 1-N-(4-methylpentan-2-yl)-4-N-Phenylbenzene-1,4-diamine
Synonyms:1,4-Benzenediamine, N~1~-(1,3-dimethylbutyl)-N~4~-phenyl- ; 1,4-Benzenediamine, N~1~-(1,3-dimethylbutyl)-N~4~-phenyl- ; N-(1,3-dimethylbutyl)-N'-Phenylbenzene-1,4-diamine ; N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine ; N-(4-Methyl-2-pentanyl)-N'-phenyl-1,4-benzenediamine
Product Categories: Industrial/Fine Chemicals;Antidegradants
Molecular Structure :
Molecular Formula: C18H24N2
Molecular Weight : 268.40
CAS NO: 793-24-8
EINECS: 212-344-0
Mol File: 793-24-8.mol
Melting point: 45-46 ºC
Boiling point: 260 ºC
Flash point: 204 ºC
Density: 1.039 g/cm3
Appearance:Purple flakes
Index of Refraction: 1.599
Surface Tension: 40.9 dyne/cm
Enthalpy of Vaporization: 66.49 kJ/mol
Vapour Pressure: 5.22E-07 mmHg at 25°C
Water solubility <0.1 g/100 mL at 17 ºC
Appearance: N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine (CAS NO. 793-24-8) is gray-black solid
1.N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine (CAS NO. 793-24-8) is used for anti-ozone agents and antioxidants for natural rubber and synthetic rubber.
2.N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine (CAS NO. 793-24-8) is used for fine effectiveness on the protection of ozone and flex fatigue cracking .
Using the 4 - amino-2-aniline and methyl isobutyl ketone, catalytic,with hydrogenation condensation, Then, N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine (CAS NO. 793-24-8) is derived.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rabbit | LD50 | skin | > 7940mg/kg (7940mg/kg) | BEHAVIORAL: FOOD INTAKE (ANIMAL) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 1, Pg. 67, 1990. |
rat | LD50 | oral | 3580mg/kg (3580mg/kg) | SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE BEHAVIORAL: FOOD INTAKE (ANIMAL) GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA" | Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 1, Pg. 67, 1990. |
RTECS ST0900000
1.Air & Water Reactions :N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine may be sensitive to prolonged exposure to air. Insoluble in water.
2.Reactivity Profile :You should protect N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine (CAS NO. 793-24-8) from exposure to strong oxidizing agents such as chlorine or hydrogen peroxide. N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine will ignite if heated strongly.
3.Fire Hazard: N-(1,3-Dimethylbutyl)-N'-phenyl-p-phenylenediamine is combustible.
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