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N-(1-Methylethyl)-N'-phenyl-1,4-benzoldiamin

N-isopropyl-N'-phenyl-p-phenylenediamine

HCID 7573
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Grundinformationen

CAS
101-72-4
Standard-SMILES
CC(C)Nc1ccc(Nc2ccccc2)cc1
InChIKey
OUBMGJOQLXMSNT-UHFFFAOYSA-N
Summenformel
C15H18N2
Durchschnittliche Molmasse
226,32 g/mol
Monoisotopische Masse
226,14699858

Überblick

N-isopropyl-n'-phenyl-p-phenylenediamine appears as dark gray to black flakes or brown-black small chip-like solid with an aromatic odor. (NTP, 1992)

Namen und Bezeichner

Bevorzugter Name
N-isopropyl-N'-phenyl-p-phenylenediamine
IUPAC
1-N-phenyl-4-N-propan-2-ylbenzene-1,4-diamine
Lokaler Name
N-(1-Methylethyl)-N'-phenyl-1,4-benzoldiamin
Englischer Name
N-Isopropyl-N'-phenyl-1,4-phenylenediamine
Summenformel
C15H18N2
Molmasse
226.32

Namen und Synonyme

101-72-4N-Isopropyl-N'-phenyl-p-phenylenediamineN-isopropyl-N'-phenyl-1,4-phenylenediamineCyzone4-IsopropylaminodiphenylamineNonox ZAAntioxidant 4010NA4-Anilino-N-isopropylanilineAntigen 3cDiafen FPAntioxidant 40NAAntioxidant IP
Weitere Namen anzeigen
IPPD4010na4010 NAAntioxidant IPPDN-isopropyl-N`-phenylenediaminen-isopropyl-n-phenyl-4-phenylenediamineS-IPGIGS
Santoflex IP4-(ISOPROPYLAMINO)DIPHENYLAMINEDiaphen FPCyzone IPOrflex PPAntigene 3CFlexzone 3CElastozone 34

Datenbank-Bezeichner

CAS
101-72-4
PubChem CID
7573
DTXSID
DTXSID1025485
ChEMBL
CHEMBL1449018

Eigenschaften

Berechnete Struktureigenschaften

XLogP
4
Polarare Oberfläche (TPSA)
24,1 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
4
Schwere Atome
17
Formalladung
0
Komplexität
201

Experimentelle und physikochemische Eigenschaften

Polymers · 2 Einträge

Plastics & Rubber -> Rubber Additives

Nitrogen Compounds -> Amines, Polyaromatic

Density · 3 Einträge

1.04 (NTP, 1992) - Denser than water; will sink

1.04 @ 25 °C

1.04 g/cm³

Color/FormDark gray to black flakes
Solubility · 4 Einträge

less than 1 mg/mL at 64 °F (NTP, 1992)

Soluble in benzene and gasoline; insoluble in water.

Insoluble water; soluble in aromatic solvents

Solubility in water: none

Flash Point303 °F (NTP, 1992)
Boiling Point322 °F at 1 mmHg (NTP, 1992)
Melting Point · 3 Einträge

162 to 169 °F (NTP, 1992)

75 °C

72-76 °C

Vapor Pressure · 2 Einträge

0.00343 mmHg at 194 °F (NTP, 1992)

0.0000711 [mmHg]

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P270, P272, P273, P280, P301+P317, P302+P352, P321, P330, P333+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P270, P272, P273, P280, P301+P317, P302+P352, P321, P330, P333+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 4 Einträge

Chemical: 1,4-Benzenediamine, N-(1-methylethyl)-N'-phenyl-

1,4-Benzenediamine, N1-(1-methylethyl)-N4-phenyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,4-Benzenediamine, N1-(1-methylethyl)-N4-phenyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: N-isopropyl-N'-phenyl-p-phenylenediamine (EC: 202-969-7)

Isopropylphenyl p-phenylenediamine: Does not have an individual approval but may be used under an appropriate group standard

DOT LabelPoison
Fire Hazards · 2 Einträge

This chemical is combustible. (NTP, 1992)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Finely dispersed particles form explosive mixtures in air.

Health HazardsSYMPTOMS: Symptoms of exposure to this compound may include contact dermatitis and occupational eczema. It may be irritating to the eyes, skin and respiratory system.
Hazards Summary · 2 Einträge

Chemie und Industrie

Pharmakologische Informationen

FDA Pharmacological Classification · 6 Einträge

0M7PSL4100

N-ISOPROPYL-N'-PHENYL-1,4-PHENYLENEDIAMINE

Established Pharmacologic Class [EPC] - Standardized Chemical Allergen

Physiologic Effects [PE] - Increased Histamine Release

Physiologic Effects [PE] - Cell-mediated Immunity

Chemical Structure [CS] - Allergens

MeSH Pharmacological ClassificationNaturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues.
Absorption, Distribution and Excretion · 1 Eintrag

Urinary excretion of N-isopropyl-N'-phenyl-p-phenylenediamine (101724) (IPPD) was analyzed in 16 press operators exposed to this compound in a rubber curing workshop. A total of 22 urine samples were collected from each worker at the beginning and end of each work day over a 2 week period. ... Rapid excretion of IPPD occurred during the working day, with mean levels of IPPD in urine samples collected before and after shifts of 19.55 and 83.57 micrograms per liter (microg/l), respectively. A total of 4.4 percent of before and 28.7 percent of after shift samples showed no detectable IPPD. A second slow component of excretion was observed during the week, with mean concentrations in before shift samples rising from 10.8 to 25.8microg/l between the beginning and end of the week. In a skin absorption experiment, with one of the authors as subject, one hand was immersed in water containing IPPD for 90 minutes. IPPD levels in the urine were measured at 0, 3, 5, and 10.5 hours after exposure, and were found to be 0, 100, 350, and 570 ug/l, respectively. The excretion rate ceased 7 days after exposure. It was concluded that the kinetics of excretion of IPPD in workers exposed daily to this compound has two different components, an initially rapid one followed by a slow one, and that there are three different components of excretion kinetics after skin absorption with half times of 3, 7, and 24 hours.

Verwendung und Herstellung

Uses · 2 Einträge

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
ChEBI
CHEBI:63569
UNII
0M7PSL4100
EC Number
202-969-7
Nikkaji
J22.142B
Food Contact Substances
FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR
Physical Description · 4 Einträge

N-isopropyl-n'-phenyl-p-phenylenediamine appears as dark gray to black flakes or brown-black small chip-like solid with an aromatic odor. (NTP, 1992)

Large Crystals; Other Solid; Dry Powder

Dark grey to black solid; [Hawley] Brown, grey, or dark purple to black solid; [CHEMINFO]

DARK GREY-TO-BLACK FLAKES.

Collision Cross Section155.4 Ų [M+H]+ [CCS Type: DT; Buffer gas: N2; Ionization: ESI+; Dataset: TOXCAST; Source Identifier: DTXSID1025485]
Other Experimental PropertiesFP: 72-76 °C

Physikochemische Eigenschaften

Schmelzpunkt
72 · 72-76°C
Siedepunkt
161 °C · 161°C
Dichte
1 · 1,17 g/cm3
Dampfdruck
0.007 Pa · 0.007Pa at 20℃
Brechungsindex
1.5 · 1.5000 (estimate)
Flammpunkt
161 °C/1mm · 161°C/1mm
storage temp.
-20 °C · -20°C
Löslichkeit
Chloroform (Slightly), DMSO (Slightly, Sonicated)
Aggregatzustand
Solid
pka
6.76 · 6.76±0.32(Predicted)
Farbe
Grey to Very Dark Grey
Biologische Quelle
rabbit
Wasserlöslichkeit
0.1 g/100 · <0.1 g/100 mL at 18 ºC
Henry's Law Constant
7 · 7.0×103 mol/(m3Pa) at 25℃, HSDB (2015)
Stabilität
Stable. Combustible. Incompatible with strong oxidizing agents.
LogP
2.77 at · 2.77 at 20℃
CAS Datenbank
101 · 101-72-4(CAS DataBase Reference)
NIST chemische Informationen
P-phenylenediamine, n-isopropyl-n'-phenyl-(101-72-4)
EPA chemische Informationen
N-Isopropyl-N'-phenyl-p-phenylenediamine (101-72-4)

N-lsopropyl-N'-phenyl Paraphenylenediamine (IPPD) CAS # 101-72-4;\\ N-Cyclohexyl-N'-phenyl-Paraphenylenediamine (CPPD);\\ N,N'-Diphenyl Paraphenylenediamine ((DPPD) CAS # 74-31-7;\\ These amines are added to rubber products (tires, tubes, pipes, gaskets, flanges, boots, shoes, etc.) during manufacturing to retard degradation by oxidants and ozone. [Marks, p. 68]

A skin and eye irritant; May cause skin sensitization; [ICSC] Emergency treatment: Paraphenylenediamine; Paraphenylenediamine can cause angioneurotic edema, the most common cause of death after an overdose; Other effects after ingestion are vomiting, acute tubular necrosis, liver injury, methemoglobinemia, and seizures; p-Phenylenediamine is a skin and respiratory tract sensitizer; [HSDB] A skin, eye, and respiratory tract irritant; May cause contact dermatitis; [CAMEO] Does not readily penetrate intact skin; Not an eye or skin irritant based on animal studies; May cause skin sensitization; No data available on inhalation toxicity, respiratory sensitization, or carcinogenicity; [OECD SIDS: N-Isopropyl-N'-phenyl-p-phenylenediamine (IPPD) - 2000] See p-Phenylenediamine.

Reactive GroupAmines, Aromatic
EC ClassificationSymbol: Xn, N; R: 22-43-50/53; S: (2)-24-37-60-61
Reactivity Profile · 1 Eintrag

N-ISOPROPYL-N'-PHENYL-P-PHENYLENEDIAMINE reacts with oxidizing agents (NTP, 1992). Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Chemical DangersDecomposes on burning. This produces toxic fumes including nitrogen oxides.
Physical DangersDust explosion possible if in powder or granular form, mixed with air.
Packaging and LabellingDo not transport with food and feedstuffs.
Air and Water ReactionsMay be sensitive to heat, air, light and moisture during long term storage. Insoluble in water.

Sicherheit und Schutzausrüstung

Fire Fighting · 2 Einträge

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)

Use water spray, powder.

First Aid Measures · 4 Einträge

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth.

First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Safe StorageWell closed.
Exposure Control and Personal Protection2.0 [mg/m3], inhalable fraction[German Research Foundation (DFG)]
Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If a spill of this chemical occurs, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with acetone and transfer the dampened material to a suitable container. Use absorbent paper dampened with acetone to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with acetone followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 1 Eintrag

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Spillage Disposal · 1 Eintrag

Personal protection: chemical protection suit. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.

Isolation and EvacuationExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Eye PreventionWear safety goggles or face shield.
Fire PreventionNO open flames. Closed system, dust explosion-proof electrical equipment and lighting. Prevent deposition of dust.
Inhalation RiskNo indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20 °C.

Toxikologische Informationen

Body BurdenThe level of 4-(iso-propylamino)diphenylamine in the urine of rubber vulcanization workers were noted to be higher in the end-shift than in the before-shift sample, respective concentrations being 83.57 and 19.55 ug/l(1).
Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1.3X10+4(SRC), determined from a structure estimation method(2), indicates that 4-(iso-propylamino)diphenylamine is expected to be immobile in soil(SRC). Volatilization of 4-(iso-propylamino)diphenylamine from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.4X10-9 atm-cu m/mole(SRC), using a fragment constant estimation method(3). The estimated pKa of 4-(iso-propylamino)diphenylamine is 5.1(5), indicating that this compound will exist only slightly in the cation form(SRC). Cations generally adsorb to organic carbon and clay more strongly than their neutral counterparts. 4-(Iso-propylamino)diphenylamine is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.5X10-5 mm Hg(SRC), determined from a fragment constant method(4).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1.3X10+4(SRC), determined from an estimation method(2), indicates that the non-protonated form of 4-(iso-propylamino)diphenylamine is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 1.4X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). An estimated pKa of 5.1(8) indicates 4-(iso-propylamino)diphenylamine will exist only slightly in the cation form at pH values of 5 to 9(SRC). Cations generally adsorb to suspended solids and sediment more strongly thantheir neutral counterparts. According to a classification scheme(5), an estimated BCF of 67(SRC), from an estimated log Kow of 3.3(6), and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is moderate.

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 4-(iso-propylamino)diphenylamine, which has an estimated vapor pressure of 3.5X10-5 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase 4-(iso-propylamino)diphenylamine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 2 hours(SRC), calculated from its rate constant of 2.2X10-10 cu cm/molecule-sec at 25 °C(SRC) determined using a structure estimation method(3). Particulate-phase 4-(iso-propylamino)diphenylamine may be removed from the air by wet and dry deposition(SRC).

Adverse Effects · 2 Einträge

Skin Sensitizer - An agent that can induce an allergic reaction in the skin.

Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.

Exposure RoutesThe substance can be absorbed into the body by inhalation of its aerosol and by ingestion.
Signs and Symptoms · 2 Einträge

Redness.

Redness. Pain.

ICSC Environmental DataThe substance is very toxic to aquatic organisms. The substance may cause long-term effects in the aquatic environment.
Soil Adsorption/Mobility · 1 Eintrag

Using a structure estimation method based on molecular connectivity indices(1), the Koc for 4-(iso-propylamino)diphenylamine can be estimated to be 1.3X10+4(SRC). According to a classification scheme(2), this estimated Koc value suggests that 4-(iso-propylamino)diphenylamine is expected to be immobile in soil(SRC). The estimated pKa of 4-(iso-propylamino)diphenylamine is 5.1(3), indicating that this compound will exist only slightly in the cation form and cations generally adsorb to organic carbon and clay more strongly than their neutral counterparts.

Human Toxicity Excerpts · 5 Einträge

A study of the prevalence of HLA antigens in persons sensitized to N-isopropyl-N'-phenyl-p-phenylenediamine was conducted to determine if an association between N-isopropyl-N'-phenyl-p-phenylenediamine sensitivity and the gene product of theHLA complex exists. The cohort consisted of 32 Czech patients sensitized to N-isopropyl-N'-phenyl-p-phenylenediamine, as determined by patch tests. The comparisons consisted of 159 persons from the general Slovak population who were unrelated to the patients. Blood samples were collected and serological typing for HLA-A, HLA-B, HLA-C and the HLA-Dw antigens HLA-Dw1, HLA-Dw2, HLA-Dw3, HLA-Dw4, HLA-Dw5, HLA-Dw7, HLA-Dw8, hLA-Dw9, HLA-Dw10, and HLA-Dw11 was performed. The prevalence of HLA-Dw3 in thecohort was significantly elevated relative to the comparisons, 37.5 versus 8.7%.The increased HLA-Dw3 prevalence was associated with a relative risk of 6.3 of developing allergy to N-isopropyl-N'-phenyl-p-phenylenediamine. The prevalence of the HLA-Dw4 antigen was nonsignificantly elevated in the cohort. The prevalence of the other HLA antigens did not differ significantly between the two groups. The authors conclude that allergy to N-isopropyl-N'-phenyl-p-phenylenediamine has a polygenetic background and that genes of theHLA antigen complex are involved.

DERMATITIS WAS CAUSED BY N-ISOPROPYL-N-PHENYL-P-PHENYLENEDIAMINE (SANTOFLEX IP).

CONTACT ALLERGIC ECZEMA AT WRIST REGION IN 9 PROFESSIONALS & 36 HOUSEWIVES IN CONTACT WITH RUBBER PARTS OF ELECTRIC IRONS PRODUCED CHARACTERISTIC COLOR CAUSED BY PETECHIAE & HEMOSIDERIN PIGMENTATION. EXAM REVEALED CAPILLARITIS. IN 5 CASES PURPURA SPREAD TO WHOLE BODY.

51 PATIENTS ALLERGIC TO IPPD WERE REVIEWED & CLINICAL FEATURES & PROGNOSIS DISCUSSED. IN 38 OF 51 PATIENTS, THE DERMATITIS WAS CONSIDERED OCCUPATIONAL, MAJORITY BEING EMPLOYED IN TRANSPORT INDUSTRY.

For more Human Toxicity Excerpts (Complete) data for 4-(ISOPROPYLAMINO)DIPHENYLAMINE (10 total), please visit the HSDB record page.

Artificial Pollution Sources4-(Iso-propylamino)diphenylamine's production and use as an antiozonant and antioxidant may result in its release to the environment through various waste streams(SRC).
Environmental Bioconcentration · 1 Eintrag

An estimated BCF of 67 was calculated for 4-(iso-propylamino)diphenylamine(SRC), using an estimated log Kow of 3.3(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate.

Volatilization from Water/Soil · 1 Eintrag

The Henry's Law constant for 4-(iso-propylamino)diphenylamine is estimated as 1.4X10-9 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 4-(iso-propylamino)diphenylamine is expected to be essentially nonvolatile from water and moist soil surfaces(2). 4-(Iso-propylamino)diphenylamine is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.5X10-5 mm Hg(SRC), determined from a fragment constant method(3).

Environmental Abiotic Degradation · 1 Eintrag

The rate constant for the vapor-phase reaction of 4-(iso-propylamino)diphenylamine with photochemically-produced hydroxyl radicals has been estimated as 2.2X10-10 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of approximately 2 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1).

Sicherheitsdaten

tsca
TSCA listed
ridadr
3077
hs_code
29215900
RTECS-Nr.
ST2650000
risk_code
36/37/38-50/53-43-22
Toxizität
LD50 oral in rat: 720mg/kg
hazard_code
Xi,N,Xn
hazard_note
Irritant
safety_code
26-36-61-60-37-24
hazard_class
9
packing_group
III
Giftige Stoffe Daten
101-72-4(Hazardous Substances Data)

Used to protect rubber against oxidation, ozone, and contamination by copper and manganese; [Hawley] Occupational exposures are mainly to rubber tires; [Kanerva, p. 1805]

Protection of rubbers against oxidation, ozone, flexcracking, and poisoning by copper and manganese.

U.S. Imports · 2 Einträge

(1979) 2.11X10+8 GRAMS (PRINCPL CUSTMS DISTS)

(1981) 2.40X10+7 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 3 Einträge

2023: 250,000 - <400,000 lb

(1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS

(1981) PROBABLY GREATER THAN 2.27X10+6 GRAMS

Consumer UsesAntioxidant
Industry UsesAntioxidant
Methods of Manufacturing · 2 Einträge

REACTION OF P-CHLORONITROBENZENE WITH ANILINE TO YIELD P-NITRODIPHENYLAMINE WHICH IS REDUCTIVELY ALKYLATED WITH ACETONE OVER A NICKEL/CHROMIUM CATALYST

Acetone + p-aminodiphenylamine (reductive amination)

Formulations/Preparations · 2 Einträge

"Flexzone" /is/ trademark for a series of antiozonants, antioxidants and stabilizers based on para-phenylenediamine. /Flexzone/

"Santoflex" /is/ trademark for a series of rubber antioxidants and antiozonants. /Santoflex/

General Manufacturing Information · 3 Einträge

Synthetic Rubber Manufacturing

1,4-Benzenediamine, N1-(1-methylethyl)-N4-phenyl-: ACTIVE

ELIMINATION OF ANTIOXIDANT 4010NA FROM RUBBER IS RECOMMENDED FOR ARTICLES WHICH CONTACT SKIN. A CHANGE IN DESIGN OF ELECTRIC IRONS IS SUGGESTED.

Anwendungen

VerwendenProtection of rubbers against oxidation, ozone, flex-cracking, and poisoning by copper and manganese.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

AcetonKaliumcarbonatAnilinkupferchromitWasserstoffPropan-2-ol4-Amino-diphenylamin

Anbieter100 Anbieter

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Ergänzende Hinweise

DefinitionChEBI: The N-substituted diamine that is 1,4-phenylenediamine substituted at one N with an isopropyl group and at the other with a phenyl group.