P-TOLUIDINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
IDENTIFIERS
1708-Toluidines 1708-Toluidines, liquid 1708-Toluidines, solid 3451-Toluidines, solid
SYNONYM REFERENCE
- (CHRIS , 1997; HSDB , 1997; Lewis, 1996; RTECS , 1997)Bretherick, 1995;(Ashford, 1994; NFPA, 1994; Lewis, 1993; ACGIH, 1991; Hathaway et al, 1991; Budavari, 1996; ITI, 1988)
USES/FORMS/SOURCES
p-Toluidine is used in the synthesis of various dyes and organic chemicals; in the preparation of ion exchange resins; and as a reagent for lingnin, nitrite, and phloroglucinol (Clayton & Clayton, 1994; (Lewis, 1993; ACGIH, 1991; Hathaway et al, 1991; Budavari, 1996).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- p-Toluidine may be toxic by inhalation and ingestion, and can be absorbed through intact skin. It is a severe skin and eye irritant.
- CNS depression, seizures, cyanosis, methemoglobinemia, hemorrhagic cystitis with painful frequent micturition, hematuria, and anuria may be noted. Gastrointestinal symptoms include nausea, vomiting, and diarrhea.
- Other symptoms may include defatting dermatitis, weakness, headache, drowsiness, dyspnea, hypotension, and jaundice.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
FIRST AID EYE EXPOSURE - Immediately wash the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately. Contact lenses should not be worn when working with this chemical. DERMAL EXPOSURE - Immediately wash the contaminated skin with soap and water. If this chemical penetrates the clothing, immediately remove the clothing, wash the skin with soap and water, and get medical attention promptly. INHALATION EXPOSURE - Move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration. Keep the affected person warm and at rest. Get medical attention as soon as possible. ORAL EXPOSURE - If this chemical has been swallowed, get medical attention immediately. TARGET ORGANS - Eyes, skin, blood, and cardiovascular system (National Institute for Occupational Safety and Health, 2007).
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. Exposed skin and eyes should be copiously flushed with water. Because of the potential for rapid onset of CNS depression or seizures with possible aspiration of gastric contents, EMESIS SHOULD NOT BE INDUCED. Cautious gastric lavage followed by administration of activated charcoal may be of benefit if the patient is seen soon after the exposure.
INHALATION EXPOSURE - INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm. If bronchospasm and wheezing occur, consider treatment with inhaled sympathomimetic agents. Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary.
DERMAL EXPOSURE - DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999). Treat dermal irritation or burns with standard topical therapy. Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines.
EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
ORAL EXPOSURE - Because of the potential for gastrointestinal tract irritation or CNS depression, do not induce emesis. Significant esophageal or gastrointestinal tract irritation or burns may occur following ingestion. The possible benefit of early removal of some ingested material by cautious gastric lavage must be weighed against potential complications of bleeding or perforation. GASTRIC LAVAGE: Consider after ingestion of a potentially life-threatening amount of poison if it can be performed soon after ingestion (generally within 1 hour). Protect airway by placement in the head down left lateral decubitus position or by endotracheal intubation. Control any seizures first. ACTIVATED CHARCOAL: Administer charcoal as a slurry (240 mL water/30 g charcoal). Usual dose: 25 to 100 g in adults/adolescents, 25 to 50 g in children (1 to 12 years), and 1 g/kg in infants less than 1 year old. Observe patients with ingestion carefully for the possible development of esophageal or gastrointestinal tract irritation or burns. If signs or symptoms of esophageal irritation or burns are present, consider endoscopy to determine the extent of injury. SEIZURES: Administer a benzodiazepine; DIAZEPAM (ADULT: 5 to 10 mg IV initially; repeat every 5 to 20 minutes as needed. CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed) or LORAZEPAM (ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist. CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue). Consider phenobarbital or propofol if seizures recur after diazepam 30 mg (adults) or 10 mg (children greater than 5 years). Monitor for hypotension, dysrhythmias, respiratory depression, and need for endotracheal intubation. Evaluate for hypoglycemia, electrolyte disturbances, and hypoxia.
METHEMOGLOBINEMIA: Determine the methemoglobin concentration and evaluate the patient for clinical effects of methemoglobinemia (ie, dyspnea, headache, fatigue, CNS depression, tachycardia, metabolic acidosis). Treat patients with symptomatic methemoglobinemia with methylene blue (this usually occurs at methemoglobin concentrations above 20% to 30%, but may occur at lower methemoglobin concentrations in patients with anemia, or underlying pulmonary or cardiovascular disorders). Administer oxygen while preparing for methylene blue therapy. METHYLENE BLUE: INITIAL DOSE/ADULT OR CHILD: 1 mg/kg IV over 5 to 30 minutes; a repeat dose of up to 1 mg/kg may be given 1 hour after the first dose if methemoglobin levels remain greater than 30% or if signs and symptoms persist. NOTE: Methylene blue is available as follows: 50 mg/10 mL (5 mg/mL or 0.5% solution) single-dose ampules and 10 mg/1 mL (1% solution) vials. Additional doses may sometimes be required. Improvement is usually noted shortly after administration if diagnosis is correct. Consider other diagnoses or treatment options if no improvement has been observed after several doses. If intravenous access cannot be established, methylene blue may also be given by intraosseous infusion. Methylene blue should not be given by subcutaneous or intrathecal injection. NEONATES: DOSE: 0.3 to 1 mg/kg. Concomitant use of methylene blue with serotonergic drugs, including serotonin reuptake inhibitors (SRIs), selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), norepinephrine-dopamine reuptake inhibitors (NDRIs), triptans, and ergot alkaloids may increase the risk of potentially fatal serotonin syndrome.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
Exposure to an airborne concentration 40 ppm of toluidine (all isomers) for 60 minutes produced severe intoxication. Prolonged exposure to as low an airborne concentration as 10 ppm caused symptoms of illness. There are no published epidemiological studies of workers exposed solely to p-toluidine (ACGIH, 1991).
- Carcinogenicity Ratings for CAS106-49-0 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A3 ; Listed as: p-Toluidine A3 :Confirmed Animal Carcinogen with Unknown Relevance to Humans: The agent is carcinogenic in experimental animals at a relatively high dose, by route(s) of administration, at site(s), of histologic type(s), or by mechanism(s) that may not be relevant to worker exposure. Available epidemiologic studies do not confirm an increased risk of cancer in exposed humans. Available evidence does not suggest that the agent is likely to cause cancer in humans except under uncommon or unlikely routes or levels of exposure.
EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Ca ; Listed as: p-Toluidine MAK (DFG, 2002): Category 3B ; Listed as: p-Toluidine Category 3B : Substances for which in vitro or animal studies have yielded evidence of carcinogenic effects that is not sufficient for classification of the substance in one of the other categories. Further studies are required before a final decision can be made. A MAK value can be established provided no genotoxic effects have been detected. (Footnote: In the past, when a substance was classified as Category 3 it was given a MAK value provided that it had no detectable genotoxic effects. When all such substances have been examined for whether or not they may be classified in Category 4, this sentence may be omitted.)
NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS106-49-0 (U.S. Environmental Protection Agency, 2011):
CHRIS, 1997 HSDB, 1997 Lewis, 1996 RTECS, 1997 Clayton & Clayton, 1994; ACGIH, 1991 ITI, 1988
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS106-49-0 (American Conference of Governmental Industrial Hygienists, 2010):
Editor's Note: The listed values are recommendations or guidelines developed by ACGIH(R) to assist in the control of health hazards. They should only be used, interpreted and applied by individuals trained in industrial hygiene. Before applying these values, it is imperative to read the introduction to each section in the current TLVs(R) and BEI(R) Book and become familiar with the constraints and limitations to their use. Always consult the Documentation of the TLVs(R) and BEIs(R) before applying these recommendations and guidelines.
- AIHA WEEL Values for CAS106-49-0 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS106-49-0 (National Institute for Occupational Safety and Health, 2007):
Listed as: p-Toluidine REL: IDLH: Not Listed
- OSHA PEL Values for CAS106-49-0 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS106-49-0 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS106-49-0 (U.S. Environmental Protection Agency, 2010):
Listed as: p-Toluidine Final Reportable Quantity, in pounds (kilograms): Additional Information: Listed as: Benzenamine, 4-methyl- Final Reportable Quantity, in pounds (kilograms): Additional Information:
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS106-49-0 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS106-49-0 (U.S. Environmental Protection Agency, 2010b):
Listed as: Benzenamine, 4-methyl- P or U series number: U353 Footnote: Listed as: p-Toluidine P or U series number: U353 Footnote: Editor's Note: The D, F, and K series waste numbers and Appendix VIII to Part 261 -- Hazardous Constituents were not included. Please refer to 40 CFR Part 261.
- EPA SARA Title III, Extremely Hazardous Substance List for CAS106-49-0 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS106-49-0 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS106-49-0 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS106-49-0 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 1708 (49 CFR 172.101, 2005):
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 3451 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN1708 (ICAO, 2002):
Proper Shipping Name: Toluidines, liquid UN Number: 1708 Proper Shipping Name: Toluidines, solid UN Number: 1708
- ICAO International Shipping Name for UN3451 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS106-49-0 (NFPA, 2002):
Listed as: p-Toluidine Hazard Ratings: Health Rating (Blue): 3 (3) Seriously toxic material. Short term exposure could cause serious temporary or residual injury even though prompt medical treatment is given. Includes known or suspect small animal carcinogens, mutagens, or teratogens.
Flammability Rating (Red): 2 Instability Rating (Yellow): 0 Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
HANDLING
- Broken packages/containers should not be handled unless by persons outfitted with appropriate protective clothing (HSDB , 1997).
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Store p-toluidine in a dry, cool, well-ventilated place; store outdoors or in a detached storage area (NFPA, 1994; ITI, 1988). Protect containers from physical damage (ITI, 1988). Store away from heat, oxidizers, and other initiators (eg, sparks, flames, or sunlight) (AAR, 1994; (NFPA, 1994; ITI, 1988).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection. fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Appropriate protective clothing should be worn to prevent skin contact (NIOSH , 1997; NFPA, 1994; ITI, 1988).
- If skin contamination occurs, immediately wash the skin with large amounts of water (NIOSH , 1997; NFPA, 1994; ITI, 1988).
- Workers should avoid breathing vapors or dusts (AAR, 1994).
- This material is toxic by skin absorption--protective clothing should be worn! Contact the material supplier for protection equipment recommendations (Mansdorf SZ, 1996).
EYE/FACE PROTECTION
- Wear appropriate eye protection, chemical safety goggles and face shield, to prevent contact (CHRIS , 1997; NIOSH , 1997; ITI, 1988).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
- Wear a positive pressure self-contained breathing apparatus (CHRIS , 1997) AAR, 1994; (NFPA, 1994; ITI, 1988)
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 106-49-0.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004) Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
p-Toluidine is a combustible solid which may burn when exposed to heat, flame, or oxidizers (CHRIS , 1997; NFPA, 1994; Lewis, 1996). Keep sparks, flames, and other sources of ignition away (AAR, 1994). It can react vigorously with oxidizing materials (Lewis, 1996). Shut off ignition sources, keep all unnecessary people away from fire, and isolate hazard area and deny entry (CHRIS , 1997; HSDB , 1997). During combustion, p-toluidine emits toxic fumes of oxides of nitrogen (Lewis, 1996) AAR, 1994)
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS106-49-0 (NFPA, 2002):
Listed as: p-Toluidine Flammability Rating: 2
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Dry chemical, CO2, alcohol-resistant foam or water spray. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- NFPA Extinguishing Methods for CAS106-49-0 (NFPA, 2002):
- If p-toluidine is on fire or involved in a fire, do not extinguish the fire unless the flow can be stopped (HSDB , 1997).
- A fine spray or fog can be used to prevent the fire from spreading and to absorb some of its heat (HSDB , 1997) AAR, 1994; (NFPA, 1994).
- Solid streams of water may be ineffective (HSDB , 1997). Apply water from as far a distance as possible (AAR, 1994).
- To fight a fire involving this compound, use foam, dry chemicals, water, or carbon dioxide (CHRIS , 1997; Lewis, 1996; NFPA, 1994).
- Flooding quantities of water can be utilized to cool fire-exposed containers (CHRIS , 1997; HSDB , 1997) AAR, 1994; (NFPA, 1994).
- Water may be an ineffective method for fighting a fire (CHRIS , 1997).
- Wear a positive pressure self-contained breathing apparatus when fighting fires (AAR, 1994).
DUST/VAPOR HAZARD
- When heated to decomposition p-toluidine emits highly toxic fumes of oxides of nitrogen (Lewis, 1996) AAR, 1994).
REACTIVITY HAZARD
- Urben (1995) identified no specific reactivity hazards for this substance.
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas.
- AIHA ERPG Values for CAS106-49-0 (AIHA, 2006):
- DOE TEEL Values for CAS106-49-0 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Toluidine, p- (4-Methylbenzenamine) TEEL-0 (units = mg/m3): 2 TEEL-1 (units = mg/m3): 15 TEEL-2 (units = mg/m3): 125 TEEL-3 (units = mg/m3): 150 Definitions: TEEL-0: The threshold concentration below which most people will experience no adverse health effects. TEEL-1: The airborne concentration (expressed as ppm [parts per million] or mg/m(3) [milligrams per cubic meter]) of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic, nonsensory effects. However, these effects are not disabling and are transient and reversible upon cessation of exposure. TEEL-2: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience irreversible or other serious, long-lasting, adverse health effects or an impaired ability to escape. TEEL-3: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience life-threatening adverse health effects or death.
- AEGL Values for CAS106-49-0 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS106-49-0 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 153 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection. fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
Avoid contact with liquid (CHRIS , 1997). Stay upwind. Stop or control the leak, if possible. Water spray can be utilized to cool and disperse vapors and protect personnel. Isolate runoff and discharged material for proper disposal (CHRIS , 1997) AAR, 1994; (NFPA, 1994). Build dikes to contain flow (AAR, 1994). Keep material out of water sources and sewers (AAR, 1994). Notify the local health and pollution control agencies (CHRIS , 1997).
Dissolve in a combustible solvent such as alcohols or benzene. Spray the solvent into a furnace with an afterburner and a scrubber. Or, pour p-toluidine into a (9:1) mixture of sand and soda ash. Place mixture in a paper carton and stuff with packing paper for fuel. Burn in a furnace (ITI, 1988). Keep upwind (AAR, 1994; (ITI, 1988). Waste management activities associated with material disposition are unique to individual situations. Proper waste characterization and decisions regarding waste management should be coordinated with the appropriate local, state, or federal authorities to ensure compliance with all applicable rules and regulations.
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- This compound may be released in wastewater during its production and use in the manufacture of dyes. It is also present in tobacco smoke and may be released during the thermal degradation of polyurethane products (HSDB , 1997).
ENVIRONMENTAL FATE AND KINETICS
SURFACE WATER Biodegradation, oxidation, and photo-oxidation are thought to be significant routes. Some adsorption to sediment may occur (HSDB , 1997).
TERRESTRIAL Biodegradation, oxidation, and chemical binding to soil compounds are thought to be the major degradation routes (HSDB , 1997).
ABIOTIC DEGRADATION
- This compound is sensitive to oxidation, degrades in sunlight, and reacts with oxygen under irradiation (HSDB , 1997).
BIODEGRADATION
- In wastewater p-toluidine was easily decomposed by activated sludge (HSDB , 1997).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- Effect of low concentration on aquatic life is unknown; compound may prove hazardous if it enters water intakes; notify local health and wildlife officials, and operators of nearby water intakes (CHRIS , 1997) AAR, 1994).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- p-Toluidine exists as white to colorless, solid, lustrous flakes, plates, or leaflets (Budavari, 1996; Lewis, 1996; NIOSH , 1997) AAR, 1994; (Ashford, 1994) Clayton & Clayton, 1994; (ACGIH, 1991).
- It has an aromatic, wine-like odor and a burning taste (NIOSH , 1997) AAR, 1994; Clayton & Clayton, 1994).
- This compound is a clear to light-yellow liquid (Hathaway et al, 1991).
PH
VAPOR PRESSURE
- 1 mmHg (at 42 degrees C) (Clayton & Clayton, 1994; (ACGIH, 1991; ITI, 1988)
- 1 mmHg (at 42 degrees C) (Lewis, 1996)
- 1 mmHg (at 20 degrees C) (NFPA, 1994)
- 1 mmHg (at 108 degrees F) (NIOSH , 1997)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
1.046 (20/4 degrees C) (Lewis, 1996; Lewis, 1993; Budavari, 1996) 0.9619 (20/4 degrees C) (Clayton and Clayton, 1994) 0.973 (50/50 degrees C) (Clayton and Clayton, 1994)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
0.9619 g/cm(3) (at 20 degrees C) (CHRIS , 1997) 1.046 g/cm(3) (at 20 degrees C) (CHRIS , 1997) Clayton & Clayton, 1994; (ACGIH, 1991; ITI, 1988)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
44.5 degrees C (112.1 degrees F) (CHRIS , 1997) 317.7 degrees K (CHRIS , 1997)
42 degrees C (Lewis, 1996) 42 to 44 degrees C (Ashford, 1994) 44 degrees C (111 degrees F) (NIOSH , 1997; NFPA, 1994; ACGIH, 1991) 44 to 45 degrees C (Clayton & Clayton, 1994; (Budavari, 1996; ITI, 1988) 44.5 degrees C (Lewis, 1996; Lewis, 1993) 45 degrees C (Lewis, 1993)
BOILING POINT
- 200.6 degrees C (1 ATM); 393 degrees F (1 ATM); 473.6 degrees K (1 ATM) (CHRIS , 1997)
- 199-202 degrees C (Ashford, 1994)
- 200 degrees C (ACGIH, 1991)
- 200-201 degrees C (Budavari, 1996; ITI, 1988)
- 200.3 degrees C (Lewis, 1993)
- 200.4 degrees C (Lewis, 1992)
- 200.5 degrees C (Clayton & Clayton, 1994)
- 201 degrees C (391 degrees F) (NFPA, 1994)
- 393 degrees F (NIOSH, 1996)
- 82.2 degrees (at 10 mmHg) (Lewis, 1996)
FLASH POINT
- 86 degrees C (closed cup) (Clayton & Clayton, 1994; (ACGIH, 1991; Budavari, 1996)
- 87.2 degrees C (189 degrees F) (Lewis, 1993)
- 88 degrees C (190 degrees F) (NFPA, 1994)
- 188 degrees F (closed cup) (CHRIS , 1997; Lewis, 1996; NIOSH , 1997; Budavari, 1996)
AUTOIGNITION TEMPERATURE
- 482 degrees C (NFPA, 1994; ITI, 1988)
- 899 degrees C (CHRIS , 1997)
- 900 degrees F (NFPA, 1994; Lewis, 1996)
EXPLOSIVE LIMITS
SOLUBILITY
p-Toluidine is slightly soluble in water (ACGIH, 1991; CHRIS , 1997; Lewis, 1996; Ashford, 1994; Lewis, 1993; ITI, 1988). Soluble in about 135 parts water (Budavari, 1996) Solubility: 0.74 in water at 21 degrees C (Clayton & Clayton, 1994) Solubility in water: 0.7% (by weight) (NIOSH , 1997) Not soluble in water (NFPA, 1994).
It is freely miscible with alcohol, ether, acetone, methanol, carbon disulfide, oils, dilute acids (Budavari, 1996; Lewis, 1996) Clayton & Clayton, 1994; (Lewis, 1993; ACGIH, 1991; ITI, 1988) and oxygenated solvents (Ashford, 1994). Solubility: 156 in alcohol at 30 degrees C (Clayton & Clayton, 1994)
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = 1.39 (HSDB , 1997)
OTHER/PHYSICAL
1.5636 (20 degrees C/D) (HSDB , 1997) 1.5532 (ITI, 1988) 1.55324 (59.1 degrees C) (Clayton & Clayton, 1994)
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