HYDROXYLAMINE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
HYDROXYLAMINE HYDROXYL AMMONIUM OXAMMONIUM
IDENTIFIERS
Editor's Note: This material is not listed in the Emergency Response Guidebook. Based on the material's physical and chemical properties, toxicity, or chemical group, a guide has been assigned. For additional technical information, contact one of the emergency response telephone numbers listed under Public Safety Measures.
SYNONYM REFERENCE
- (Budavari, 2000)CHRIS, 2001;(Hathaway et al, 1996)RTECS, 2001
USES/FORMS/SOURCES
Hydroxylamine is used as a reducing agent in photography, leather tanning, and polymer manufacturing, as well as in the production of other chemicals (Hathaway, 1996; OHM/TADS, 2001). Hydroxylamine is used to stabilize natural rubber and to prevent formation of objectionable odors and tastes when refining fatty materials (Hathaway, 1996). Hydroxylamine is used in organic synthesis (Lewis, 1997). Hydroxylamine is used in processing color photographs, in oxime synthesis, manufacture of bactericides, fungicides, and algicides, in the manufacture of rubber, plastics, nylon, and cosmetics (Baran, 1991), in aldehyde and ketone purification, as a dehairing agent, and as an antioxidant for fatty acids and soaps (Derelanko et al, 1987).
Hydroxylamine may be stored and shipped in a liquid form, as hydroxylamine sulfate or hydroxylamine hydrochloride (NFPA, 1997). Hydroxylamine may exist as large white flakes or white needles, or as a colorless liquid. It is very hygroscopic (HSDB, 2001; OHM/TADS, 2001). Hydroxylamine exists as 100% pure grade (CHRIS, 2001).
Hydroxylamine may be produced by the interaction of hydroxylamine hydrochloride and sodium butoxide, or by reacting nitric oxide (NO) and hydrogen (H2) (HSDB, 2001). Hydroxylamine is also produced by the electrolytic reduction of nitric acid, by the action of sodium bisulfate on sodium nitrate, and via platinum catalyzed hydrogenation of nitric oxide at atmospheric pressure, in the presence of 10% hydrochloric acid (HCl) (HSDB, 2001). Hydroxylamine may be derived by decomposing hydroxylamine hydrochloride or hydroxylamine sulfate with a base and then distilling in a vacuum (Lewis, 1997).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Hydroxylamine may be irritating to the eyes, skin, and mucous membranes. The solution can be corrosive when in contact with the skin. Signs and symptoms of exposure may include headache, vertigo, restlessness, tinnitus, dyspnea, nausea, vomiting, proteinuria, hematuria, methemoglobinemia, anemia, leucocytosis, platelet aggregation, jaundice, and splenomegaly. Large doses may result in seizures, hypotension, or respiratory arrest.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (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 154 (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.
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.
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 seizures, DO NOT induce emesis. PREHOSPITAL ACTIVATED CHARCOAL ADMINISTRATION Consider prehospital administration of activated charcoal as an aqueous slurry in patients with a potentially toxic ingestion who are awake and able to protect their airway. Activated charcoal is most effective when administered within one hour of ingestion. Administration in the prehospital setting has the potential to significantly decrease the time from toxin ingestion to activated charcoal administration, although it has not been shown to affect outcome (Alaspaa et al, 2005; Thakore & Murphy, 2002; Spiller & Rogers, 2002). In patients who are at risk for the abrupt onset of seizures or mental status depression, activated charcoal should not be administered in the prehospital setting, due to the risk of aspiration in the event of spontaneous emesis. The addition of flavoring agents (cola drinks, chocolate milk, cherry syrup) to activated charcoal improves the palatability for children and may facilitate successful administration (Guenther Skokan et al, 2001; Dagnone et al, 2002).
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. 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. HYPOTENSION: Infuse 10 to 20 mL/kg isotonic fluid. If hypotension persists, administer dopamine (5 to 20 mcg/kg/min) or norepinephrine (ADULT: begin infusion at 0.5 to 1 mcg/min; CHILD: begin infusion at 0.1 mcg/kg/min); titrate to desired response. 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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
The LD50 by ingestion is 50 to 500 mg/kg (CHRIS, 2001). Hydroxylamine is very toxic. An amount between 1 teaspoon and 1 ounce is the probable lethal dose for a 70 kg (150 pound) person (HSDB, 2001).
MAXIMUM TOLERATED EXPOSURE
The maximum tolerated human exposure to this agent has not been delineated. ANEMIA - Chronic absorption of about 1 milligram/kilogram may lead to slight anemia (ILO, 1971).
Doses of 100 to 500 milligrams per kilogram for one to 6 weeks produced histological changes in liver, heart, spleen, kidney, stomach, intestine, lung, and bladder (Sami, 1980).
- Carcinogenicity Ratings for CAS7803-49-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed 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): Not Listed MAK (DFG, 2002): Not Listed 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 CAS7803-49-8 (U.S. Environmental Protection Agency, 2011):
References: Budavari, 2000 Hathaway, 1996; ITI, 1995 OHM/TADS, 2001; RTECS, 2001) LD- (INTRAVENOUS)RABBIT: LD- (SUBCUTANEOUS)RABBIT: LD50- (ORAL)DOG: LD50- (INTRAPERITONEAL)MOUSE: LD50- (INTRAPERITONEAL)RAT: TDLo- (INTRAPERITONEAL)RAT:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS7803-49-8 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS7803-49-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS7803-49-8 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS7803-49-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS7803-49-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS7803-49-8 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS7803-49-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS7803-49-8 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS7803-49-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS7803-49-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS7803-49-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS7803-49-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions (49 CFR 172.101, 2005):
- ICAO International Shipping Name (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS7803-49-8 (NFPA, 2002):
Listed as: Hydroxylamine Hazard Ratings: Health Rating (Blue): 2 Flammability Rating (Red): [blank cell] Instability Rating (Yellow): [blank cell] Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
SUMMARY
It is recommended that handling processes of hydroxylamine be mechanized so human contact is avoided (HSDB, 2001). Hydroxylamine should be kept separate from oxidizing materials (NFPA, 1997).
HANDLING
- It is recommended that handling processes of hydroxylamine be mechanized so human contact is avoided (HSDB, 2001).
- Hydroxylamine should be handled with caution (HSDB, 2001).
- Open airtight containers of hydroxylamine periodically to relieve pressure from decomposition products. The decomposition products include nitrogen and ammonia or nitrogen oxides (OHM/TADS, 2001; (Sittig, 1991).
- Hydroxylamine is extremely unstable, and will decompose at room temperature in the presence of atmospheric moisture and carbon dioxide (HSDB, 2001).
STORAGE
Hydroxylamine should be stored and shipped in lead-lined steel drums (NFPA, 1997) OHM/TADS, 2001). Containers of hydroxylamine should be protected against physical damage (OHM/TADS, 2001; (Sittig, 1991). Hydroxylamine will attack some metals (Sittig, 1991).
- ROOM/CABINET RECOMMENDATIONS
Storage areas should be kept cool, dry, and well-ventilated (NFPA, 1997). Material should be stored away from sunlight, heat, and oxidizers (NFPA, 1997). It is recommended that storage areas be either outside or detached (NFPA, 1997). It is recommended that anhydrous hydroxylamine be stored at 10 degrees C. This is done to prevent internal oxidation-reduction reactions which may occur at ambient temperatures (Urben, 1999).
Hydroxylamine should be kept separate from oxidizing materials (NFPA, 1997). Hydroxylamine is incompatible with pyridine and carbonyls, and will have vigorous reactions with hypochlorites (Lewis, 2000). Hydroxylamine is incompatible with zinc powder and oxidants (Sittig, 1991). Hydroxylamine is incompatible with the following (Pohanish & Greene, 1997): strong acids organic anhydrides isocyanates aldehydes sodium zinc
There is an explosion risk when hydroxylamine is mixed with the following substances (ITI, 1995):
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (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 in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Protective clothing, including positive pressure self-contained breathing apparatus should be worn by all emergency response personnel (NFPA, 1997).
- Butyl rubber gloves should be worn when handling hydroxylamine (ITI, 1995).
EYE/FACE PROTECTION
- Safety glasses and face/ body shield should be used (ITI, 1995).
- Hydroxylamine is a corrosive irritant to the eyes (Lewis, 2000).
RESPIRATORY PROTECTION
- A positive pressure self-contained breathing apparatus should be worn by all emergency response personnel (NFPA, 1997).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 7803-49-8.
-PHYSICAL HAZARDS
FIRE HAZARD
Editor's Note: This material is not listed in the Emergency Response Guidebook. Based on the material's physical and chemical properties, toxicity, or chemical group, a guide has been assigned. For additional technical information, contact one of the emergency response telephone numbers listed under Public Safety Measures. POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004) Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
Hydroxylamine may explode when it is exposed to heat or flames. Therefore, extreme caution should be used when approaching a fire involving hydroxylamine. A fire should only be fought using remotely activated fire extinguishing equipment. The surrounding area should be evacuated (Sittig, 1991). When exposed to oxidizers, flame, or heat, hydroxylamine is a dangerous fire hazard. If a large surface area of hydroxylamine, such as precipitate on paper, is exposed to air, it may spontaneously ignite (Lewis, 2000). Hydroxylamine is very unstable and will decompose at room temperature by atmospheric moisture and carbon dioxide (ITI, 1995).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS7803-49-8 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (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 154 (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 CAS7803-49-8 (NFPA, 2002):
- Use fire extinguishing agent suitable for any surrounding fire. Fire should be fought from a protected location, or the maximum possible distance. Explosive decomposition may occur under fire conditions (NFPA, 1997).
EXPLOSION HAZARD
- Hydroxylamine is an explosion risk when mixed with the following substances (ITI, 1995; Lewis, 2000):
- Hydroxylamine is a noncombustible solid which will explode when heated to 129 degrees C (265 degrees F). It will also explode when exposed to open flames (NFPA, 1997) Urben, 1999).
- Hydroxylamine will explode in air if it is heated to above 70 degrees C, and is also explosive under confinement (Lewis, 2000) OHM/TADS, 2001).
- Fires and explosions may be caused by strong oxidizers (Sittig, 1991).
- Explosive decomposition may occur when hydroxylamine is mixed with contaminants or exposed to temperatures above 150 degrees F/65 degrees C (Pohanish & Greene, 1997).
DUST/VAPOR HAZARD
- Hydroxylamine will release toxic fumes of nitrous oxides when heated to decomposition (Lewis, 2000).
REACTIVITY HAZARD
- Hydroxylamine decomposes rapidly at room temperatures (Lewis, 2000).
- Hydroxylamine is self-reactive (NFPA, 1997; Pohanish & Greene, 1997).
- Hydroxylamine will ignite on contact with Barium dioxide; Barium oxide; Chlorine; Copper sulfate; Lead dioxide; Phosphorus pentachloride; Phosphorus trichloride; Potassium dichromate; Sodium; and Zinc (HSDB, 2001; (Lewis, 2000)
- Hydroxylamine hydrochloride slowly decomposes when moist (Windholz, 1983).
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 154 (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 154 (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 154 (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 CAS7803-49-8 (AIHA, 2006):
- DOE TEEL Values for CAS7803-49-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Hydroxylamine TEEL-0 (units = mg/m3): 0.25 TEEL-1 (units = mg/m3): 0.75 TEEL-2 (units = mg/m3): 5 TEEL-3 (units = mg/m3): 25 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 CAS7803-49-8 (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 CAS7803-49-8 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (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 154 (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 in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
Spilled hydroxylamine should be absorbed in a noncombustible material, and properly disposed (NFPA, 1997). Spilled hydroxylamine can be covered with sodium bisulfite and then sprinkled with water (Sittig, 1991).
Hydroxylamine may be neutralized with bisulfate solution (OHM/TADS, 2001). Hydroxylamine is a candidate for incineration (Sittig, 1991). 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
- Hydroxylamine may be harmful to aquatic life, even in very low concentrations (CHRIS, 2001).
ABIOTIC DEGRADATION
- No information found at the time of this review.
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
LC50 - (WATER) FATHEAD MINNOW: 7.2 ppm for 96H - static, H2SO4, salt (OHM/TADS, 2001) LC50 - (WATER) DAPHNIA MAGNA: 1.2 ppm for 96H - static, H2SO4, salt (OHM/TADS, 2001)
- 50 ppm of hydroxylamine will be toxic to aquatic plants (OHM/TADS, 2001).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Hydroxylamine may exist as large white flakes or white needles, or as a colorless liquid (HSDB, 2001).
- Hydroxylamine is odorless (CHRIS , 2002).
PH
- Forms alkaline solution (CHRIS , 2002).
VAPOR PRESSURE
- HYDROXYLAMINE: 10 mmHg (at 47 degrees C) (Lewis, 2000; NFPA, 1997)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
1.2255 (at 0/4 degrees C) (Budavari, 2000) 1.204 (at 40/4 degrees C) (Budavari, 2000) 1.227 (at room temperature) (CHRIS , 2002)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
DENSITY
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
32.05 degrees C (HSDB, 2001; ILO, 1998) 170 degrees C (for crystals) (HSDB, 2001) 34 degrees C; 93 degrees F (Lewis, 2000; NFPA, 1997) 32 degrees C (Sittig, 1991) 33 degrees C (Budavari, 2000; Lewis, 1997) 33.05 degrees C (OHM/TADS , 2002) 33 degrees C; 92 degrees F (NFPA, 1997) 33.1 degrees C (ITI, 1995)
BOILING POINT
- 56.5 degrees C (OHM/TADS , 2002)
- 56.5 degrees C (at 22 mmHg) (HSDB, 2001; (ITI, 1995)
- 58 degrees C (at 22 mmHg) (Budavari, 2000)
- 56.5 degrees C; 133.7 degrees F; 329.7 K (at 22 mmHg) (CHRIS , 2002)
- 70 degrees C; 158 degrees F; 343.2 K (at 22 mmHg) (CHRIS , 2002)
- 70 degrees C; 158 degrees F (NFPA, 1997; Sittig, 1991)
- 110 degrees F (Lewis, 2000)
- 70 degrees C (at 60 mmHg) (ITI, 1995; Lewis, 1997)
FLASH POINT
- Hydroxylamine explodes at 265 degrees F; 129 degrees C (ITI, 1995; Lewis, 2000; Sittig, 1991)
- 265 degrees F (open cup) (CHRIS , 2002)
AUTOIGNITION TEMPERATURE
- 265 degrees F (CHRIS , 2002)
SOLUBILITY
Hydroxylamine is very soluble in water, and will decompose in hot water (Budavari, 2000; NFPA, 1997).
Hydroxylamine is soluble in acid and liquid ammonia (Budavari, 2000). Hydroxylamine is sparingly soluble in ether, carbon disulfide, and chloroform (Budavari, 2000). The solubility of hydroxylamine in the higher alcohols will decrease with increasing molecular weight (Budavari, 2000). Hydroxylamine is very soluble in methanol (Budavari, 2000).
OTHER/PHYSICAL
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