313949-90-5Nc1ccc(N)cc1CBCKQZAAMUWICA-UHFFFAOYSA-NP-phenylenediamine appears as a white to purple crystalline solid (melting point 234 F) that turns purple to black in air. Flash point 309 F. Toxic by skin absorption, inhalation or ingestion. Used for production of aramid fiber, antioxidants, as a laboratory reagent, in photographic developing, and as a dye for hair and furs.
313949-90-5CHEMBL403741CHEBI:51403Hazardous Air Pollutants (HAPs)
Nitrogen Compounds -> Amines, Aromatic
Cosmetics ingredient -> Colorant; Other (Specify)
Cosmetic ingredients (p-Phenylenediamine) -> CIR (Cosmetic Ingredient Review)
Hair dyeing
log Kow= -0.25
-0.3
Greater than 1 (water= 1)
Relative density (water = 1): 1.1
>1 no temp
WHITE TO SLIGHTLY RED CRYSTALS
WHITE PLATES FROM BENZENE, ETHER
4 % at 75 °F (NIOSH, 2024)
SOL IN 100 PARTS COLD WATER; SOL IN ALCOHOL, CHLOROFORM, ETHER
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Danger
H301: Toxic if swallowed [Danger Acute toxicity, oral]
P261, P262, P264, P264+P265, P270, P271, P272, P273, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P321, P330, P333+P317, P337+P317, P361+P364, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Danger
H301+H311+H331 (43.2%): Toxic if swallowed, in contact with skin or if inhaled [Danger Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]
P260, P261, P262, P264, P264+P265, P270, P271, P272, P273, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P308+P316, P316, P321, P330, P333+P317, P337+P317, P361+P364, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Chemical: 1,4-Benzenediamine
Hazard Traits - Hazard Trait Undefined
1,4-Benzenediamine is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,4-Benzenediamine 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: 06-12-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/14562
1,4-Phenylenediamine: Does not have an individual approval but may be used under an appropriate group standard
The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)
FROM STUDIES OF THE INTRACUTANEOUS SENSITIZATION OF GUINEA-PIGS USING PARA-PHENYLENEDIAMINE, HYDROQUINONE, QUINHYDRONE AND BENZOQUINONE, IT HAS BEEN SUGGESTED THAT BENZOQUINONE FORMATION PLAYS AN IMPORTANT ROLE IN THE ALLERGIC ACTION OF PARA-PHENYLENEDIAMINE.
P-PHENYLENEDIAMINE YIELDS P-QUINONE PROBABLY IN MAN, MONKEY, PIG, HORSE, SHEEP, GOAT, CAT, RABBIT, GUINEA PIG, RAT, MOUSE, & HEN. /FROM TABLE/
P-PHENYLENEDIAMINE YIELDS P-QUINONE PROBABLY IN HORSERADISH ... WITH CERULOPLASMIN & LACCASE. /FROM TABLE/
P-PHENYLENEDIAMINE YIELDS P-QUINONE PROBABLY IN PERIPLANETA, ... IN CITRUS, ... IN TEA. /FROM TABLE/
N,N'-DIACETYL-PARA-PHENYLENEDIAMINE WAS IDENTIFIED AS A URINARY METABOLITE OF PARA-PHENYLENEDIAMINE IN DOGS.
U770QIT64J
P-PHENYLENEDIAMINE
Established Pharmacologic Class [EPC] - Standardized Chemical Allergen
Physiologic Effects [PE] - Increased Histamine Release
Physiologic Effects [PE] - Cell-mediated Immunity
Chemical Structure [CS] - Allergens
PARAPHENYLENEDIAMINE HYDROCHLORIDE WAS APPLIED TO THE SKIN OF DOGS IN GELS AND FLUIDS, AS THEY ARE USED IN HAIR DYEING; ABSORPTION WAS DETERMINED BY COMPARING BLOOD CONCENTRATIONS WITH THAT OBTAINED AFTER IV INJECTION OF THE DIAMINE OVER A COMPARABLE PERIOD OF TIME. IT WAS CALCULATED THAT 16 MG WERE ABSORBED WHEN 50 ML OF A LAURYL SULFATE-BASED GEL CONTAINING 1.5 G PARAPHENYLENEDIAMINE WAS APPLIED FOR 3 HOURS AND FREE ACCESS TO AIR WAS ALLOWED (THE MAXIMAL BLOOD CONCENTRATION WAS 0.15 UG/ML). THIS AMOUNT ROSE TO 110 MG IF THE TREATED AREA WAS IMMEDIATELY COVERED WITH ALUMINUM FOIL (THE MAXIMAL BLOOD CONCENTRATION WAS 0.5 UG/ML). /P-PHENYLENEDIAMINE HYDROCHLORIDE/
Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.
Wird geladen…
SOL IN HOT BENZENE
Water solubility= 38,000 ppm
Solubility in water, g/100ml at 25 °C: 4
(75 °F): 4%
311 °F (NTP, 1992)
311 °F
156 °C c.c.
312 °F
312 °F
513 °F at 760 mmHg (NTP, 1992)
267 °C
267 °C
513 °F
267 °C @760 [mm Hg]
513 °F
Toxic gases and vapors (such as oxides of nitrogen and carbon monoxide) may be released in a fire involving p-phenylenediamine.
When heated to decomposition it emits acrid smoke and irritating fumes.
Excerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Finely dispersed particles form explosive mixtures in air. Risk of fire and explosion on contact with strong oxidizing agents.
p-Phenylenediamine is primarily used as a dye intermediate and as a dye. Acute (short-term) exposure to high levels of p-phenylenediamine may cause severe dermatitis, eye irritation and tearing, asthma, gastritis, renal failure, vertigo, tremors, convulsions, and coma in humans. Eczematoid contact dermatitis may result from chronic (long-term) exposure in humans. In rats and mice chronically exposed to p- phenylenediamine in their diet, depressed body weights, but no other clinical signs of toxicity, were observed in several studies. No information is available on the reproductive, developmental, or carcinogenic effects of p-phenylenediamine in humans. EPA has not classified p-phenylenediamine with respect to carcinogenicity.
An important dye used for permanent hair coloring, the dye itself (but not the dyed hair) can cause allergic contact dermatitis. [Marks, p. 111] Immunologic contact urticaria documented; [Kanerva, p. 219] In animal experiments, intraperitoneal injections induce methemoglobinemia, and chronic feeding causes fatty degeneration of the liver. Liver injury after occupational exposure has been reported. [ACGIH] Potential adverse effects include asthma, allergic contact dermatitis, methemoglobinemia, and kidney injury; [ICSC]
TSCA CHIPs present a preliminary assessment of 1,4-Benzenediamine's potential for injury to human health & the environment (available at EPA's TSCA Assistance Office: (202) 554-1404.
Waters MD et al; The Genetic Toxicology of Gene-Tox Non-Carcinogens; Mutat Res 205(1-4): 139-82 (1988).
USEPA; PHENYLENEDIAMINES; RESPONSE TO INTERAGENCY TESTING COMMITTEE; FED REGIST 47(5) 973 (1982). EVIDENCE IS GIVEN SUPPORTING TESTING OF THE CLASS OF COMPOUNDS PHENYLENEDIAMINES FOR THEIR TOXIC EFFECTS ON HUMAN HEALTH AND THE ENVIRONMENT. THE RESULTS OF TOXICITY TESTING OF 22 COMPOUNDS ARE TABULATED AS ARE THE EFFECTS FOR WHICH TESTING IS BEING CONSIDERED FOR 13 COMPOUNDS, AND THE USES OR POTENTIAL USES OF 47 PHENYLENEDIAMINES.
Fukunaga T, et al; Contact Dermat 35 (3): 185-6 (1996). Contact anaphylaxis due to para-phenylenediamine.
Yagi H et al; Hum Exp Toxicol 15 (8): 617-18 (1996). Paraphenylenediamine induced optic atrophy following hair dye poisoning.
Excerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Use water spray, powder.
Fresh air, rest. Half-upright position. Refer for medical attention.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again. 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. Give a slurry of activated charcoal in water to drink. Refer for medical attention .
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.
(General first aid procedures)
Keep well closed and protected from light.
IN GENERAL MATERIALS ... TOXIC AS STORED OR WHICH CAN DECOMP INTO TOXIC COMPONENTS ... SHOULD BE STORED IN COOL ... VENTILATED PLACE, OUT OF ... SUN, AWAY FROM ... FIRE HAZARD ... /AND/ BE PERIODICALLY INSPECTED & MONITORED. INCOMPATIBLE MATERIALS SHOULD BE ISOLATED.
The following wastewater treatment technologies have been investigated for p-phenylenediamine: biological treatment.
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.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. 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. Do NOT absorb in saw-dust or other combustible absorbents.
SRP: Contaminated protective clothing should be segregated in such a manner so that there is no direct personal contact by personnel who handle, dispose, or clean the clothing. Quality assurance to ascertain the completeness of the cleaning procedures should be implemented before the decontaminated protective clothing is returned for reuse by the workers. Contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.
The worker should immediately wash the skin when it becomes contaminated.
The worker should wash daily at the end of each work shift.
Work clothing that becomes wet or significantly contaminated should be removed and replaced.
For more Preventive Measures (Complete) data for 1,4-BENZENEDIAMINE (6 total), please visit the HSDB record page.
TERRESTRIAL FATE: Based on a recommended classification scheme(1), an estimated Koc value of 16(SRC), determined from a measured log Kow of -0.30(2), and a recommended regression-derived equation(3), indicates that 1,4-benzenediamine is expected to have high mobility in soil(SRC); however it may form covalent bonds to humic material which would limit movement through soil(4). Volatilization of 1,4-benzenediamine is not expected from moist soil surfaces(SRC) given an estimated Henry's Law constant of 6.7X10-10 atm-cu m/mole(SRC), using a fragment constant estimation method(5). Volatilization of 1,4-benzenediamine from dry soil surfaces is not expected(SRC) based on an extrapolated vapor pressure of 0.005 mm Hg(SRC) at 25 °C(6). Biodegradation is expected to occur slowly in soils based on standard biodegradability tests conducted with activated sludge(7-11).
AQUATIC FATE: Based on a recommended classification scheme(1), an estimated Koc value of 16(SRC), determined from a measured log Kow of -0.30(2), and a recommended regression-derived equation(3), indicates that 1,4-benzenediamine is not expected to adsorb to suspended solids and sediment in water(SRC). 1,4-benzenediamine is not expected to volatilize from water surfaces(3,SRC) based on an estimated Henry's Law constant of 6.7X10-10 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Degradation of 1,4-benzenediamine by photochemically produced peroxy radicals will be an important environmental fate process in surface waters(5,SRC). The half-life of this reaction is estimated as 1 day for a solution concentration of 1X10-9 M of peroxy radicals and an estimated rate constant of 1X10+4 L/mol-s(5). According to a classification scheme(6), an estimated BCF value of 0.3(3,SRC), from a measured log Kow of -0.3(2,SRC), suggests that bioconcentration in aquatic organisms is low(SRC). Biodegradation in aquatic environments is not expected to be an important environmental fate process(SRC). A 0% theoretical oxygen demand was observed for 1,4-benzenediamine in a Warburg apparatus during a 5 day incubation period(7). A measured pKb value of 6.2 indicates that the protonated form of 1,4-benzenediamine will exist at environmentally significant pH and this may affect the environmental fate of this compound in aquatic environments(8).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1,4-benzenediamine, which has an extrapolated vapor pressure of 0.005 mm Hg at 25 °C(2,SRC), is expected to exist primarily as a vapor in the ambient atmosphere. Vapor-phase 1,4-benzenediamine 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 about 2 hours(3,SRC).
The substance can be absorbed into the body by inhalation, through the skin and by ingestion.
inhalation, skin absorption, ingestion, skin and/or eye contact
Cough. Dizziness. Headache. Laboured breathing. See Ingestion.
MAY BE ABSORBED! Redness.
Redness. Pain. Swelling of the eyelids. Blurred vision. Loss of vision.
Abdominal pain. Blue lips, fingernails and skin. Convulsions. Drowsiness. Laboured breathing. Shortness of breath. Vomiting. Weakness.
irritation pharynx, larynx; bronchial asthma; sensitization dermatitis
/Annual/ physical examinations of exposed personnel, including blood counts and studies of liver function. Those persons with allergy and with diseases of skin, liver, blood, and lungs should avoid exposure. Sensitized persons should avoid re-exposure.
Based on a recommended classification scheme(1), an estimated Koc value of 16(SRC), determined from a measured log Kow of -0.3(2) and a recommended regression-derived equation(3), indicates that 1,4-benzenediamine is expected to have high mobility in soil(SRC); however it may form covalent bonds to humic material which would limit movement through soil(4).
1,4-Benzenediamine was examined for mutagenic activity in Salmonella typhimurium tester strains TA1535, TA1537, TA1538, TA100, and in Saccharomyces cerevisiae strain D3 with and without metabolic activation provided by phenobarbitol-induced rat liver S9 fraction. The test article was not mutagenic at concentrations ranging from 1 to 1000 ug/ml in the Salmonella strains (plate incorporation assay), or at 0.05% in the Saccharomyces D3 strain (mitotic recombination assay), in the presence or absence of metabolic activation. In preliminary experiments, 1,4-benzenediamine was toxic to Saccharomyces D3 cells at a concentration of 0.1%, however, toxicity to Salmonella was not reported.
para-Phenylenediamine (CAS # 106-50-3) was evaluated as cause for methemoglobinuria in sets of 2 each beagle dogs fed single gavage doses of 1.0, 3.0, and 10.0 mg/kg bodyweight. All dogs exhibited lacrimation, while 10.0 mg/kg dosed dogs showed red and swollen eyes persisting in one dog at 24-hour post-gavage observation. Slight redness was also noted in the eyes of 3.0 mg/kg dogs, but all such signs were resolved by 24 hours after treatment. Methemoglobinemia was not induced at levels producing pharmacotoxic effects in beagle dogs.
1,4-Phenylenediamine (CAS # 106-50-3) was evaluated for neurotoxic effects in groups of Crl:CDBR rats (12/sex/group) administered single gavage doses in sterile water of 0, 20, 40, and 80 mg/kg bodyweight. Neurotoxicity was assessed by functional operational battery and motor activity tests performed prior to treatment (baseline assessment) and at approximately 1.5 hours (time of maximal clinical signs), 24 hours, and 4 days post-gavage. Both females of all dose levels and males of 40 and 80 mg/kg dosage groups exhibited signs of a systemic toxicity with significantly reduced weight gain. These deviations from control were echoed in significantly reduced food consumption in all except 20 mg/kg females after Day 1 and in males of 80 mg/kg doses. No other clinical signs of toxicity were significantly dose-related. Upon the functional observation batteries through post-treatment Day 4, females only demonstrated significant dose-related malaise, postural changes, palpebral closure, and diminished arousal. Males showed similar functional aberrations which were not statistically significant relative to controls. Treatment was not significantly reflected in fore- or hind-limb grip strength or foot splay. Measurements of decreased motor activity in treated rats were significantly dose-related, except after Day 1 in both 20 mg/kg groups.
Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. p-Phenylenediamine is included on this list.
Manufacturers and processors of para-phenylenedimine are required to conduct health efffects, chemical fate and environmental effects testing under TSCA section 4.
Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. 1,4-Benzenediamine is included on this list.
Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 5000 lb or 2270 kg. The toll free number of the NRC is (800) 424-8802; In the Washington D.C. metropolitan area (202) 426-2675. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).
THE DISTRIBUTION KINETICS OF THE (3)H-LABELED P-PHENYLENEDIAMINE HYDROCHLORIDE WAS STUDIED WHEN ADMINISTERED IV AND WHEN APPLIED PERCUTANEOUSLY IN MICE AND RABBITS. IN RABBITS, IV ADMINISTRATION LED TO A BIPHASIC BLOOD CLEARANCE WITH T/2 VALUES OF 24 MINUTES AND 43.5 HOURS AND QUICK PERCUTANEOUS ABSORPTION. THE TISSUE DISTRIBUTION PATTERN INVESTIGATED AFTER IV AND PERCUTANEOUS ADMINISTRATION IN 16 DIFFERENT TISSUES AND ALSO IN BLOOD DID NOT DEMONSTRATE ANY TARGET ORGAN FOR SELECTIVE LOCALIZATION OF THE DYE. NO GREATER THAN 0.06% OF THE IV ADMINISTERED RADIOACTIVITY WAS MEASURED PER 10 G OF ANY TISSUE AT THE 12TH DAY. /P-PHENYENEDIAMINE HYDROCHLORIDE/
After the /dog abdominal/ skin was washed, m-phenylenediamine concentration in the blood was observed to decline more rapidly than was the case with p-phenylenediamine and 2,5-diaminotoluene.
A homologous series of hair dyes was selected for percutaneous absorption studies with excised human skin. The permeability constants obtained for the dyes were compared with octanol/water and skin membrane/water partition coefficients. The compounds examined were: p-phenylenediamine, o-phenylenediamine, 2-nitro-p-phenylenediamine, 2-amino-4-nitrophenol, 4-chloro-m-phenylenediamine, and 4-amino-2-nitrophenol. Skin absorption of the dyes was observed when they were applied in an aqueous solution. With one exception, the octanol/water partition coefficients were in the same rank order as the permeability constants. The determination of the partitioning of the hair dyes between water and either stratum corneum or epidermis was more complex. Preliminary stratum corneum/water partition studies resulted in values that were in the reverse order of skin permeation. When binding of the compounds to components of the membrane was saturated, the partition values more closely duplicated the rank order of permeability of the dyes. Prediction of percutaneous absorption of substances based on their partition coefficients may be confounded if these compounds are capable of binding to skin.
CIR ingredient: p-Phenylenediamine
p-Phenylenediamine is primarily used as a dye intermediate and as a dye (e.g., hair dyes and dyes used for dyeing furs), as well as a photographic developing agent and a chemical intermediate. p-Phenylenediamine is also used as a vulcanization accelerator and as an antioxidant in rubber compounds.
Used to dye hair and fur; also used to develop photographs and to synthesize other organic compounds; [ACGIH] Occupational asthma reported in fur dyers; [Malo] Allergic contact dermatitis in hairdressers, mechanics, printers, and textile workers; [Marks] Used to dye leather; [PMID 21938525]
Leather Tanning and Processing [Category: Industry]
Dyeing furs; also in photochemical measurements, accelerating vulcanization; manuf azo dyes.
CHEM INT FOR DYES (EG, DIRECT BLACK 19, 78 & 80); OXIDN BASE 10 & DEVELOPER 13 FOR DYES; CHEM INT FOR ARAMID FIBERS (USED IN TIRE CORD); CHEM INT FOR N,N'-DISUBSTITUTED-P-PHENYLENEDIAMINES; COMPONENT OF GASOLINE ANTIOXIDANTS.
(1978) 1.50X10+6 G (PRINCPL CUSTMS DISTS)
(1982) 9.99X10+4 G (PRINCPL CUSTMS DISTS)
2023: 10,000,000 - <50,000,000 lb
(1978) PROBABLY GREATER THAN 4.54X10+6 G
(1982) PROBABLY GREATER THAN 4.54X10+6 G
REDUCTION OF 1-AMINO-4-NITROBENZENE WITH IRON AND HYDROCHLORIC ACID.
Prepn: A. Rinne, T. Zincke, Ber. 7, 869 (1874); Ger. pat. 202,170 (1907 to BASF), C. A. 3, 382 (1909); A.J. Quick, J. Am. Chem. Soc. 42, 1033 (1920); J.F. Norris, E.O. Cummings, Ind. & Eng. Chem. 17, 305 (1925). See also: Beilstein XIII, 61 (1930).
ONE TECHNICAL GRADE OF PARA-PHENYLENEDIAMINE AVAILABLE IN THE USA HAS THE FOLLOWING SPECIFICATIONS: PURITY, 99.2% MINIMUM; MOISTURE CONTENT, 0.1% MAXIMUM; ORTHO-PHENYLENEDIAMINE (1,2-DIAMINOBENZENE) CONTENT, 0.1% MAXIMUM; AND IRON CONTENT, 50 MG/KG MAXIMUM.
Cosmetics product ingredient: p-Phenylenediamine
Information on 206 consumer products that contain p-Phenylenediamine in the following categories is provided:
Organic Fiber Manufacturing
1,4-Benzenediamine: ACTIVE
ALL COLORING AGENTS CONTAINING PARA-PHENYLENEDIAMINE OR ONE OF ITS HOMOLOGS MUST INCL STATEMENT ON PACKAGE RELATIVE TO SENSITIZING PROPERTIES ... & ITS ABILITY TO CAUSE BLINDNESS IF IT CONTACTS EYES. LAW ... REQUIRES THAT PATCH TEST BE CONDUCTED 24 HR BEFORE ... DYE IS APPLIED /TO HAIR/.
Formerly: as an eyelash dye ... sold under proprietary name Lash Lure.
VerwendenAdditive in polymer blends and liquid dispersions for corrosion resistant coatings; antistatic fabrics, coatings, and packaging; conductive inks and adhesives; printed circuit boards; radar and microwave absorption; EMI/RFI shielding; sensors.