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HCID 7564Erstellt: 25. Oktober 2026

4-Amino-diphenylamin

4-ADPA · N-PHENYL-P-PHENYLENEDIAMINE · P-AMINODIPHENYLAMINE · N1-phenylbenzene-1,4-diamine · 4-N-phenylbenzene-1,4-diamine · VARIAMINE BLUE RT · Variamine Blue RT Base · N-Phenyl-1,4-benzenediamine

https://huagongshe.com/de/chemical/7564

Molekülstruktur von 4-Amino-diphenylamin

Identifikatoren & physikalische Daten

CAS No.101-54-2
SummenformelC12H12N2
Durchschnittliche Molmasse184,24 g/mol
Monoisotopische Masse184,10004838 g/mol
SMILESNc1ccc(Nc2ccccc2)cc1
InChIKeyATGUVEKSASEFFO-UHFFFAOYSA-N
PubChem CID7564
ChEMBLCHEMBL572203
ChEBICHEBI:59038
EC No.202-951-9
DTXSIDDTXSID7025895
Lokaler Name4-Amino-diphenylamin

Chemische & physikalische Eigenschaften

XLogP2,5
Polarare Oberfläche (TPSA)38,1
H-Brücken-Donoren2
H-Brücken-Akzeptoren2
Frei drehbare Bindungen2
Schwere Atome14
Formalladung0
Komplexität156
PolymersNitrogen Compounds -> Amines, Polyaromatic
KosmetikaCosmetics ingredient -> ColorantCosmetic ingredients (N-Phenyl-p-Phenylenediamine) -> CIR (Cosmetic Ingredient Review)Hair dyeing
LogP (Verteilungskoeffizient)2.4 (calculated)
Dichte1.15 (NTP, 1992) - Denser than waterwill sink1.1 at 100 °C1.09 g/cm³
Viscosity1.76X10-2 Pa.s at 25 °C
Color/FormNeedles (alcohol)Purple powderPurple needles
Löslichkeitless than 1 mg/mL at 66 °F (NTP, 1992)Slightly soluble in water, chloroformvery soluble in ethanolsoluble in diethyl ether, ligroinSoluble in alcohol and acetoneInsoluble in watersoluble in oxygenated solventsSolubility: 500 mg/L at 20 °C and pH 8.9Solubility in water, g/100ml at 20 °C: 0.05ethanol: soluble10mg/mL, clear, very dark red (Violet to brown to black solution)Soluble in water at 20°C 0.6g/L. Soluble in (10 mg/mL) ethanol.
Flammpunkt380 °F (NTP, 1992)380 °F'193 °C193°C
Siedepunkt669 °F at 760 mmHg (NTP, 1992)354 °C
DecompositionWhen heated to decompostion it emits toxic fumes of NOx.
Schmelzpunkt163 to 167 °F (NTP, 1992)75 °C69 °C
Dampfdruck0.0000121 [mmHg]1.21X10-5 mm Hg at 25 °C (extrapolated)Vapor pressure, Pa at 20 °C: 0.0000761 hPa
Brechungsindex1.6266 (estimate)
LagerbedingungenStore below +30°C.
pKa (Säurekonstante)5.20±0.10(Predicted)
AggregatzustandLiquid
FarbeClear
pH8.9 (0.5g/l, H2O, 20℃)
BRN908935
Henry-Konstante1.5×103 mol/(m3Pa) at 25℃, Yaws (2003)
StabilitätStable. Combustible. Incompatible with strong oxidizing agents, strong acids, plastics.
Kosmetik-Inhaltsstoffe FunktionenHAIR DYEING
InChI1S/C12H12N2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,14H,13H2
InChIKeyATGUVEKSASEFFO-UHFFFAOYSA-N
SMILESNc1ccc(Nc2ccccc2)cc1
LogP (Verteilungskoeffizient)1.82 at 20℃ and pH7
CAS Datenbank101-54-2(CAS DataBase Reference)
NIST chemische Informationen1,4-Benzenediamine, N-phenyl-(101-54-2)
EPA chemische Informationenp-Aminodiphenylamine (101-54-2)

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (97.2%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P264, P264+P265, P270, P272, P273, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P333+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 680 reports by companies from 21 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.H302: Harmful if swallowed [Warning Acute toxicity, oral]
Regulatorische InformationenChemical: 1,4-Benzenediamine, N-phenyl-1,4-Benzenediamine, N1-phenyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,4-Benzenediamine, N1-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)Status: Active Update: 10-05-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/147314-Aminodiphenylamine: Does not have an individual approval but may be used under an appropriate group standard
Weitere SicherheitsinformationenIMAP assessments - 1,4-Benzenediamine, N-phenyl and a salt: Human health tier II assessment
DOT-KennzeichnungPoison
BrandgefahrenThis chemical is combustible. (NTP, 1992)
GesundheitsgefahrenSYMPTOMS: Symptoms of exposure to this compound may include irritation of the eyes and upper respiratory tract. It may also cause irritation of the skin and mucous membranes. Other symptoms include headache, dizziness and methemoglobinemia with symptoms of cyanosis including bluish discoloration of the lips, earlobes and fingernails. Dermatitis has been reported.
GefahrenübersichtPotential adverse effects form using this hair dye include dermatitis, eye injury, and liver damage. [HSDB] When it was used in hair dyes, sensitization was relatively low in hairdressers[Kanerva, p. 1749] A skin and eye irritantMay cause skin sensitizationCan induce methemoglobinemia if ingested[ICSC] Skin designationDanger of skin sensitization3B carcinogen[MAK]
Reaktive GruppeAmines, Aromatic
Special ReportsBioassay of p-Aminodiphenylamine for Possible Carcinogenicity (1978) Technical Rpt Series No. 82 DHEW Pub No. (NIH) 78-1332, U.S. Department of Health Education and Welfare, National Cancer Institute, Bethesda, MD 20014[Available from, as of April 4, 2003: http://ntp.niehs.nih.gov/ntp/htdocs/LT_rpts/tr082.pdf]European Commission, ESISIUCLID Dataset, p-aminodiphenylamine (101-54-2) (2000 CD-ROM edition).[Available from, as of March 1, 2009: http://esis.jrc.ec.europa.eu/]
Reactivity ProfileN-PHENYL-P-PHENYLENEDIAMINE is incompatible with strong oxidizers. It is also incompatible with strong acids. It may react with plastics. (NTP, 1992)
Chemical DangersOn combustion, forms toxic fumes of carbon monoxide and nitrogen oxides. Reacts with strong acids and strong oxidants.
Air and Water ReactionsInsoluble in water.
Hazard Classes and CategoriesAcute Tox. 4 (97.2%)Acute toxicity - category 4Acute toxicity (Oral) - Category 4
BrandbekämpfungFires 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 dry powder, carbon dioxide.
Erste-Hilfe-MaßnahmenFresh air, rest. Refer for medical attention.Remove contaminated clothes. Rinse skin with plenty of water or shower.First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.Rinse mouth. Give one or two glasses of water to drink. Do NOT induce vomiting. Refer for medical attention .
Erste HilfeEYES: 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.
Sichere LagerungSeparated from strong oxidants and strong acids. Dry.
Freisetung ohne BrandSMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol 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.
EntsorgungsverfahrenSRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air qualitypotential migration in soil or watereffects on animal, aquatic, and plant lifeand conformance with environmental and public health regulations.
Verschüttetes entsorgenPersonal protection: particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting.
Isolation and EvacuationExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Eye PreventionWear safety spectacles or eye protection in combination with breathing protection if powder.
Fire PreventionNO open flames.
Inhalation RiskA harmful concentration of airborne particles can be reached quickly when dispersed, especially if powdered.
Skin PreventionProtective clothing. Protective gloves.
ÖkotoxizitätswerteEC50Species: Daphnia magna (Water flea, age <24 hr)Conditions: freshwater, static, pH 7.8-8.1, dissolved oxygen 96-99% saturatedConcentration: 1220 ug/L for 24 hr (95% confidence interval: 520-2920 ug/L)Effect: intoxication, immobilization /98% purity/Conditions: freshwater, renewal, pH 7.8-8.1, dissolved oxygen 96-99% saturatedConcentration: 370 ug/L for 48 hrSpecies: Daphnia magna (Water flea)Conditions: static not aerated, 20.4 °C, pH 7.9 + or -0.1, dissolved oxygen 8.3-8.9 mg/LConcentration: 4.1 mg/L for 24 hrEffect: immobilization /98.8% purity/Conditions: static unaerated, 19.8-21.5 °C, pH 7.5-9.7, dissolved oxygen 8.4-14.4 mg/LConcentration: 0.1 mg/L for 21 daysEffect: reproduction rate /98.8% purity/For more Ecotoxicity Values (Complete) data for P-AMINODIPHENYLAMINE (7 total), please visit the HSDB record page.
UmweltverhaltenTERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 3.1X10+3(SRC), determined from a structure estimation method(2), indicates that p-aminodiphenylamine is expected to have slight mobility in soil(SRC). The pKa of p-aminodiphenylamine is 5.20(3), indicating that this compound will partially exist in cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4). Volatilization of p-aminodiphenylamine from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 3.7X10-10 atm-cu m/mole(SRC), using a fragment constant estimation method(5). p-Aminodiphenylamine is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.21X10-5 mm Hg at 25 °C(6). Reported inherent biodegradation values of 28% after 20 days in an adapted activated sludge and 58% after 3 hours in a mixed, non-adapted activated sludge inoculum(7) suggest that biodegradation in the aquatic environment may be an important fate process(SRC).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 3.1X10+3(SRC), determined from a structure estimation method(2), indicates that p-aminodiphenylamine 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 3.7X10-10 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). A pKa of 5.20(5) indicates p-aminodiphenylamine will exist partially in the cation form at pH values of 5 to 9 and therefore volatilization from water surfaces is not expected to be an important fate process(6). According to a classification scheme(7), an estimated BCF of 5.1(SRC), from an estimated log Kow of 1.82(8) and a regression-derived equation(9), suggests the potential for bioconcentration in aquatic organisms is low. Reported inherent biodegradation values of 28% after 20 days in an adapted activated sludge and 58% after 3 hours in a mixed, non-adapted activated sludge inoculum(10) suggest that biodegradation in the aquatic environment may be an important fate process(SRC).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), p-aminodiphenylamine, which has a vapor pressure of 1.21X10-5 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase p-aminodiphenylamine 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 1.9 hours(SRC), calculated from its rate constant of 2.0X10-10 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase p-aminodiphenylamine may be removed from the air by wet or dry deposition(SRC). p-Aminodiphenylamine contains chromophores that absorb at wavelengths >290 nm(4) and therefore may be susceptible to direct photolysis by sunlight(SRC).
Unerwünschte WirkungenOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
ExpositionspfadeThe substance can be absorbed into the body by inhalation and by ingestion.
ToxizitätsübersichtOn the basis of the data included in this report, the CIR Expert Panel concludes that N-Phenyl-p-Phenylenediamine... safe for use in hair dyes at concentrations up to 1.7% (as the free base).Safe for use in cosmetics, with qualifications
Signs and SymptomsRedness. Pain.Blue lips, fingernails and skin. Confusion. Convulsions. Dizziness. Headache. Nausea. Abdominal pain. Vomiting. Unconsciousness.
Ongoing Test StatusThe following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical.[Available from: http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=101-54-2]
ICSC Environmental DataThis substance may be hazardous to the environment. Special attention should be given to aquatic organisms.
Soil Adsorption/MobilityUsing a structure estimation method based on molecular connectivity indices(1), the Koc of p-aminodiphenylamine can be estimated to be 3.1X10+3(SRC). According to a classification scheme(2), this estimated Koc value suggests that p-aminodiphenylamine is expected to have slight mobility in soil. The pKa of p-aminodiphenylamine is 5.20(3), indicating that this compound will partially exist in cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4).
Human Toxicity Excerpts/HUMAN EXPOSURE STUDIES/ A study of contact dermatitis in Italian hairdressers was conducted in a cohort of 302 hairdressers (43 men and 259 women, mean age 24.6 years) who were treated for skin problems at Italian dermatology clinics over a 5 year period. Of these, 184 were patch tested with an Italian standard allergen series and a hairdresser's allergen series. ... The subjects had been employed as hairdressers a mean of 5.3 years. ... Among hair dye allergens, p-phenylenediamine, para-aminodiphenylamine, o-nitro-p-phenylenediamine, and para-toluenediamine caused a high incidence of positive reactions, 24.2, 10.6, 7.9, and 13.2%, respectively. ... It was concluded that a high proportion of hairdressers who seek treatment for skin problems have allergic contact dermatitis./HUMAN EXPOSURE STUDIES/ A cleaner at a chemical plant suffering from allergic skin reaction of the face, neck and arms was tested. Positive reaction to 0 25% test substance in petrolatum after 48 and 72 hr./HUMAN EXPOSURE STUDIES/ Cosmetic intolerance has been studied in 5202 patientstested for possible contact dermatitis. Results: 107 (2.1%) showed positive reaction to the test substancefrom 156 patients with pure allergy to cosmetics 5 (3.2%) -reacted positve to the test substance./HUMAN EXPOSURE STUDIES/ Tests were performed in 181 persons with confirmed group sensitization to aromatic amino compoundstest concentration 1% of the test substanceresults: 96 patients (53%) showed positive reaction.For more Human Toxicity Excerpts (Complete) data for P-AMINODIPHENYLAMINE (8 total), please visit the HSDB record page.
Artificial Pollution Sourcesp-Aminodiphenylamine's production and use as a dye intermediate(1) may result in its release to the environment through various waste streams(SRC).
Environmental BiodegradationAEROBIC: p-Aminodiphenylamine, present at 2.4 mg/L biodegraded 0, 24, and 28% in 5, 10, and 20 days, respectively, using an adapted activated sludge inoculum in a DEV test(1). p-Aminodiphenylamine, present at 100 mg DOC/L, reached 58% DOC after 3 hours using a mixed, non-adapted activated sludge inoculum in a Zahn-Wellens test(1).
F8
Wassergefährdungsklasse (WGK)3
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN3077
Zollcode29215990
RTECS-Nr.ST3150000
R-Sätze (R)22-36-43-42/43-36/37/38-20/22-50/53
ToxizitätLD50 orally in Rabbit: 464 mg/kg LD50 dermal Rabbit > 5000 mg/kg
GefahrensymboleXn,Xi,N
hazard_noteIrritant
Sicherheitshinweise (S)26-36-45-36/37/39-61-60-36/37
Gefahrenklasse9Acute Tox. 4 OralAquatic Chronic 2Eye Irrit. 2Skin Sens. 1
VerpackungsgruppeIII
Lagerklasse11 - Combustible Solids
Gefahrstoffdaten101-54-2(Hazardous Substances Data)
Selbstentzündungstemperatur>500 °C

Anwendungen & Verwendung

Beschreibung

p-Aminodiphenylamine hydrochloride was formerly used as a hair dye. Sensitization, when deteeted by patch testing, is relatively low in hairdressers.

Verwenden

4-Aminodiphenylamine is used as an oxidation dye color in hair dyes. It is also promoted as an efficient reagent for oxidase enzymes, including glucose, lactate, xanthine, and lysine oxidases.