GLYCERIN
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
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
- (Ariel Global View, 2001;(Ashford, 1994; Budavari, 2000; HSDB , 2001; Lewis, 2000; RTECS , 2001)
USES/FORMS/SOURCES
It is one of the main ingredients in the production of nitroglycerin (dynamite). Since it is hygroscopic, glycerin is a common ingredient in skin lotions, cosmetics, soaps and is used to condition tobacco and textiles. Its sweet taste has led to its use as a sweetener and in liqueurs and confectioneries. Glycerin is also used as a solvent and emulsifier and may be found in inks, adhesives, pharmaceuticals, and binders. As a plasticizer it is used in the manufacture of plastics and resins. It may also be used as antifreeze and for nutrients in the fermentation process (Ashford, 1994; Budavari, 2000; Lewis, 1997).
Grades or forms of glycerin include: natural, synthetic, USP, CP, saponification soap lye, crude yellow distilled, high gravity or dynamite, and FCC (Lewis, 1997). Commercial grades are available containing 80% to 99.5% glycerol in water (Ashford, 1994).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
Glycerin may be irritating to the eyes, skin, and mucous membranes. CNS depression and seizures may also occur. Ingestion may result in insomnia, nausea, vomiting, diarrhea, fever, elevated blood sugar, and diabetic coma. Large doses may cause irritation and dehydration of tissues, hemolysis, renal failure, hemoglobinuria, and paralysis.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
Inhalation of material may be harmful. Contact may cause burns to skin and eyes. Inhalation of Asbestos dust may have a damaging effect on the lungs. Fire may produce irritating, corrosive and/or toxic gases. Some liquids produce vapors that may cause dizziness or suffocation. Runoff from fire control may cause pollution.
ACUTE CLINICAL EFFECTS
Glycerin is nontoxic after ingestion, except with very large doses, when it can cause headache, dizziness, nausea, vomiting, thirst, diarrhea, and confusion (HSDB , 2001). Glycerin is rapidly absorbed after ingestion and is distributed mostly to body fat (HSDB , 2001). Glycerin had no systemic effects in humans after skin application (HSDB , 2001). If it comes in direct contact with the eye, glycerin can cause stinging, burning sensation, tearing, and redness, but no injury (Grant & Schuman, 1993). Severe dehydration, cardiac arrhythmias, and hyperosmolar nonketoic coma have been reported and may be fatal (HSDB , 2001).
Glycerin has strong osmotic effects, the basis for its action as a laxative in suppositories and in lowering the intraocular pressure with large oral doses (HSDB , 2001). Glycerin has often been used as a negative control or vehicle for other substances in toxicology studies.
- ANIMAL STUDIES - It was a mild skin irritant in rabbits (RTECS).
CHRONIC CLINICAL EFFECTS
Glycerin is a competitive inhibitor of succinic dehydrogenase in the Krebs tricarboxylic acid cycle. Oxalate could be formed both from excess succinate and also from glycerin itself. NTP studies: Glycerin, when tested three times in the Salmonella assay, gave negative results on two occasions and inconclusive results on the third testing (ACGIH, 1997).
Reproductive: Intratesticular injection of glycerin in rats resulted in antispermatogenic activity, but this unique route of administration is not considered relevant to occupational exposure to gylcerin (ACGIH, 1997). When given to rats at a concentration of 5 percent in the drinking water for 6 months, glycerin caused calcification in the renal tubules (Anderson, 1950). In another rat drinking water study, it increased urinary levels of oxalic acid (Haag & Ambrose, 1937).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. 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. Ensure that medical personnel are aware of the material(s) involved, and take precautions to protect themselves.
FIRST AID 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. ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed.
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 CNS depression or seizures, DO NOT induce emesis. 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. 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.
ACUTE LUNG INJURY: Maintain ventilation and oxygenation and evaluate with frequent arterial blood gases and/or pulse oximetry monitoring. Early use of PEEP and mechanical ventilation may be needed.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
- Carcinogenicity Ratings for CAS56-81-5 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Glycerin mist ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Glycerin mist 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 ; Listed as: Glycerin (mist) 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 CAS56-81-5 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS56-81-5 (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 CAS56-81-5 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS56-81-5 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS56-81-5 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
Listed as: Glycerin (mist) (Total dust) Table Z-1 for Glycerin (mist) (Total dust): 8-hour TWA: ppm: mg/m3: 15 Ceiling Value: Skin Designation: No Notation(s): Not Listed
Listed as: Glycerin (mist) (Respirable fraction) Table Z-1 for Glycerin (mist) (Respirable fraction): 8-hour TWA: ppm: mg/m3: 5 Ceiling Value: Skin Designation: No Notation(s): Not Listed
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS56-81-5 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS56-81-5 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS56-81-5 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS56-81-5 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS56-81-5 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS56-81-5 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS56-81-5 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS56-81-5 (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 CAS56-81-5 (NFPA, 2002):
Listed as: Glycerine Hazard Ratings: Health Rating (Blue): 1 Flammability Rating (Red): 1 Instability Rating (Yellow): 0 Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Glycerin is hygroscopic and may also absorb hydrogen sulfide, hydrogen cyanide, and sulfur dioxide (Budavari, 2000). Explosive and hazardous reactions occur when glycerine is mixed with the following (Budavari, 2000) Lewis, 2000; (NFPA, 1997; Urben, 1999): acetic anhydride aniline + nitrobenzene calcium hypochlorite chlorine (if heated and confined) chromic anhydride chromic oxide chromium trioxide ethylene oxide + heat hydrogen peroxide lead oxide + fluorine nitric + sulfur acids nitric acid + hydrofluoric acid (storage hazard) nitrobenzene perchloric acid + lead oxide phosphorous triiodide potassium chlorate potassium permanganate silver perchlorate potassium peroxide sodium hydride sodium peroxide sodium tetraydroborate
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
- Wear appropriate chemical protective clothing, including gloves, boots, and goggles, when handling glycerin or if there is a potential for exposure. If exposure occurs, wash skin with soap and water and flush eyes with water for 15 minutes (AAR, 2000).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 56-81-5.
-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 171 (ERG, 2004) Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot.
Pure glycerin is fairly stable, though it may burn if exposed to heat or flame (Lewis, 2000; OHM/TADS, 2001). Though classified as a combustible liquid, it requires effort to ignite. However, glycerin may react violently with oxidizers, especially solids, and form explosive mixtures with other chemicals. As a viscous liquid, glycerin can form good contact with potential reactants. Its viscosity and high boiling point prevent the dissipation of oxidative heat (AAR, 2000; (Urben, 1999).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS56-81-5 (NFPA, 2002):
Listed as: Glycerine Flammability Rating: 1
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
Water spray, fog or regular foam. Move containers from fire area if you can do it without risk. Do not scatter spilled material with high pressure water streams. Dike fire-control water for later disposal.
- TANK FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
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 CAS56-81-5 (NFPA, 2002):
- Fight fires involving glycerin with alcohol foam, carbon dioxide, or dry chemical extinguishing agents. Water fog may also be used. Foam or water may lead to frothing. Fires should be extinguished from as far away as possible. If the compound is not burning, any fire-exposed containers should be kept cool and away from any flame or spark (AAR, 2000; (CHRIS , 2001; Lewis, 2000; ITI, 1995; Sittig, 1991).
EXPLOSION HAZARD
- Explosion may occur if glycerin comes in contact with strong oxidizers such as chromium trioxide, potassium chlorate, calcium hypochlorite, or potassium permanganate. Mixtures of glycerin and hydrogen peroxide are explosive. Explosive glyceryl nitrate is formed from a mixture of glycerin and nitric and sulfuric acids. Perchloric acid, lead oxide and glycerin form perchlorate esters which may be explosive. Glycerin and chlorine may explode if heated and confined (Budavari, 2000; Lewis, 2000; NFPA, 1997; Urben, 1999).
DUST/VAPOR HAZARD
- Glycerin vapors are not irritating. However, glycerin mist may be irritating to eyes and respiratory tract (CHRIS , 2001; Sittig, 1991).
REACTIVITY HAZARD
- Explosive and hazardous reactions occur when glycerine is mixed with the following (Budavari, 2000) Lewis, 2000; (NFPA, 1997; Urben, 1999):
acetic anhydride aniline + nitrobenzene calcium hypochlorite chlorine (if heated and confined) chromic anhydride chromic oxide chromium trioxide ethylene oxide + heat hydrogen peroxide lead oxide + fluorine nitric + sulfur acids nitric acid + hydrofluoric acid (storage hazard) nitrobenzene perchloric acid + lead oxide phosphorous triiodide potassium chlorate potassium permanganate potassium peroxide silver perchlorate sodium hydride sodium peroxide sodium tetraydroborate
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 171(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 171 (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 171 (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.
- AIHA ERPG Values for CAS56-81-5 (AIHA, 2006):
- DOE TEEL Values for CAS56-81-5 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Glycerine (mist); (Glycerol, glycerin) TEEL-0 (units = mg/m3): 15 TEEL-1 (units = mg/m3): 125 TEEL-2 (units = mg/m3): 500 TEEL-3 (units = mg/m3): 500 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 CAS56-81-5 (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; 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; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; 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, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; 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National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; 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, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; 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, 2005; 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, 2005; 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, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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 CAS56-81-5 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004) Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent dust cloud. Avoid inhalation of asbestos dust.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004) Spills of glycerin should be kept out of sewers and water bodies (AAR, 2000). In water, spilled glycerin will sink and dissolve (OHM/TADS, 2001). Spills on the ground can be cleaned up using an absorbent material which is then sealed in plastic bags for disposal. Glycerin may be disposed of by incineration after mixing with a more flammable solvent (Sittig, 1991).
SMALL SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004) SMALL DRY SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 171 (ERG, 2004)
Glycerin may be disposed of by spraying into a furnace. Incineration may be aided by mixing with a more flammable solvent (ITI, 1995; 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
- Glycerin occurs naturally in mixtures of some fatty acids, but is likely to enter the environment through industrial processes or use and disposal of products. Glycerin biodegrades in water and poses little threat as an air pollutant. It creates biological oxygen demand (BOD) in water as it degrades, but does not bioaccumulate to a significant degree (HSDB , 2001; OHM/TADS, 2001).
ENVIRONMENTAL FATE AND KINETICS
Glycerin released to air may undergo gas-phase oxidation and photochemical production of hydroxyl radicals with a half-life of 33 hours. Because of its solubility in water, it may also be removed from the atmosphere by wet deposition (HSDB , 2001).
SURFACE WATER Glycerin will biodegrade in water rapidly under aerobic conditions, but would not be expected to volatilize. Biodegradation will also occur under anaerobic conditions and in seawater (HSDB , 2001). Glycerin is not expected to bioconcentrate in fish and aquatic organisms nor is it expected to absorb to sediment and suspended organic matter (HSDB , 2001).
ABIOTIC DEGRADATION
- Glycerin released to air may undergo gas-phase oxidation and photochemical production of hydroxyl radicals with a half-life of 33 hours. Because of its solubility in water, it may also be removed from the atmosphere by wet deposition (HSDB , 2001).
BIODEGRADATION
- Incubated with activated sludge from a waste water treatment plant, 94-97% of glycerin was removed in 24 hours (HSDB , 2001).
BIOACCUMULATION
Bioconcentration factors for glycerin are estimated to be 3 and 0.2, respectively, based on the octanol/water partition coefficient and solubility, indicating that bioconcentration would not be significant (HSDB , 2001).
ENVIRONMENTAL TOXICITY
- LC50 - (WATER) GOLDFISH: >5000 mg/L for 24H -- modified ASTM D 1345 (HSDB , 2001)
- LC50 - (WATER) RAINBOW TROUT FINGERLINGS: 67,500 ppm for 96H (at 12 degrees C) (OHM/TADS, 2001)
- TDLo - (WATER) PROTOZOA (Entosiphon sulcatum): 3200 mg/L -- cell multiplication inhibition test (HSDB , 2001)
- TDLo - (WATER) ALGAE (Microcystis aeruginosa): 2900 mg/L -- cell multiplication inhibition test (HSDB , 2001)
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Glycerin is a clear, colorless to pale yellow liquid or solid (below 64 degrees F) with syrupy consistency. It has a sweet, warm taste, but is odorless to having mild odor. Shiny orthorhombic crystals are formed after prolonged cooling at 0 degrees C. This compound absorbs water from air (Budavari, 2000; Lewis, 2000; NISOH , 2001; HSDB , 2001).
PH
- neutral to litmus (Budavari, 2000)
VAPOR PRESSURE
- 0.0025 mmHg (at 50 degrees C) (Lewis, 2000; OHM/TADS, 2001)
- 0.003 mmHg (at 122 degrees F) (NISOH , 2001)
- 1.58x10(-4) mmHg (at 25 degrees C) (HSDB , 2001)
- 40 mmHg (at 198 degrees C) (OHM/TADS, 2001)
SPECIFIC GRAVITY
- NORMAL TEMPERATURE AND PRESSURE
(25 degrees C; 77 degrees F and 760 mmHg) 1.26201 (at 25/25 degrees C) (Budavari, 2000) >1.249 (at 25/25 degrees C) (USP) (Lewis, 1997) 95% Aqueous Solution: 1.24910 (at 25/25 degrees C) (Budavari, 2000) 90% Aqueous Solution: 1.23585 (at 25/25 degrees C) (Budavari, 2000)
- OTHER TEMPERATURE AND/OR PRESSURE
1.26557 (at 15/15 degrees C) (Budavari, 2000) 1.26362 (at 20/20 degrees C) (Budavari, 2000) 1.260 (at 20/4 degrees C) (Lewis, 2000) 1.2613 (at 20/4 degrees C) (HSDB , 2001) 1.261 (at 20 degrees C) (CHRIS , 2001) 95% Aqueous Solution: 1.25270 (at 15/15 degrees C) (Budavari, 2000) 95% Aqueous Solution: 1.25075 (at 20/20 degrees C) (Budavari, 2000) 90% Aqueous Solution: 1.23950 (at 15/15 degrees C) (Budavari, 2000) 90% Aqueous Solution: 1.23755 (at 20/20 degrees C) (Budavari, 2000) 80% Aqueous Solution: 1.213 (at 15/15 degrees C) (Budavari, 2000) 70% Aqueous Solution: 1.185 (at 15/15 degrees C) (Budavari, 2000) 60% Aqueous Solution: 1.157 (at 15/15 degrees C) (Budavari, 2000) 50% Aqueous Solution: 1.129 (at 15/15 degrees C) (Budavari, 2000) 20% Aqueous Solution: 1.049 (at 15/15 degrees C) (Budavari, 2000) 5% Aqueous Solution: 1.0122 (at 15/15 degrees C) (Budavari, 2000)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
1.3 (NFPA, 1997) 1.2527 (OHM/TADS, 2001)
DENSITY
- NORMAL TEMPERATURE AND PRESSURE
(25 degrees C; 77 degrees F and 760 mmHg) 1.26 kg/L (Ashford, 1994; (NIOSH ICSC, 2001))
- OTHER TEMPERATURE AND/OR PRESSURE
1.2636 g/mL (at 20 degrees C) (ACGIH, 1991) 1.261 g/mL (at 20 degrees C) (CHRIS , 2001)
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
18 degrees C (Ashford, 1994) 17.9 degrees C; 64.2 degrees F; 291.1 degrees K (CHRIS , 2001) 64 degrees F (solid form melts above 64 degrees F, but liquid freezes at much lower temperature) (CHRIS , 2001; NISOH , 2001) 10% Aqueous Solution: -1.6 degrees C (Budavari, 2000) 30% Aqueous Solution: -9.5 degrees C (Budavari, 2000) 50% Aqueous Solution: -23.0 degrees C (Budavari, 2000) 66.7% Aqueous Solution: -46.5 degrees C (Budavari, 2000) 80% Aqueous Solution: -20.3 degrees C (Budavari, 2000) 90% Aqueous Solution: -1.6 degrees C (Budavari, 2000)
17.8 degrees C (ACGIH, 1991; Budavari, 2000) 18 degrees C (Lewis, 1997) 20 degrees C (HSDB , 2001) 18.2 degrees C ((NIOSH ICSC, 2001)) 17.9 degrees C (Lewis, 2000)
BOILING POINT
- 290.0 degrees C; 554 degrees F; 563 K (at 760 mmHg) (decomposition) (Budavari, 2000; CHRIS , 2001; Lewis, 2000; NISOH , 2001)
- 263.0 degrees C (at 400 mmHg) (Budavari, 2000)
- 240.0 degrees C (at 200 mmHg) (Budavari, 2000)
- 220.1 degrees C (at 100 mmHg) (Budavari, 2000)
- 208.0 degrees C (at 60 mmHg) (Budavari, 2000)
- 182.2 degrees C (at 20 mmHg) (Budavari, 2000)
- 167.2 degrees C (at 10 mmHg) (Budavari, 2000)
- 153.8 degrees C (at 5 mmHg) (Budavari, 2000)
- 125.5 degrees C (at 1.0 mmHg) (Budavari, 2000)
- 171 degrees C; 340 degrees F (NFPA, 1997)
FLASH POINT
- 176 degrees C; 350 degrees F (open cup) (Budavari, 2000)
- 160 degrees C; 320 degrees F (Lewis, 1997)
- 350 degrees F (open cup); 320 degrees F (closed cup) (CHRIS , 2001)
- 199 degrees C; 390 degrees F (NFPA, 1997)
- 177 degrees C (open cup) (HSDB , 2001; (NIOSH ICSC, 2001))
- 176.7 degrees C (OHM/TADS, 2001)
AUTOIGNITION TEMPERATURE
- 392 degrees C; 739 degrees F (Lewis, 1997)
- 698 degrees F (CHRIS , 2001; Lewis, 2000)
- 370 degrees C; 698 degrees F (NFPA, 1997; (NIOSH ICSC, 2001))
- 739 degrees F (HSDB , 2001)
SOLUBILITY
Glycerin is miscible with water (ACGIH, 1991; Budavari, 2000; Lewis, 2000). 1,220,000 mg/L (at 5 degrees C) (HSDB , 2001) 1,000,000 ppm (at 25 degrees C) (OHM/TADS, 2001)
Glycerin is miscible with alcohol and has limited solubility in ethyl acetate (1:11), ethyl ether (1:500). One gram of glycerin will is soluble in 15 mL of acetone. It is insoluble in carbon tetrachloride, carbon disulfide, benzene, chloroform, petroleum ethers, and oils, solubility in acetone 1g in 15 ml (Budavari, 2000; Lewis, 2000; HSDB , 2001).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = -1.76 (HSDB , 2001)
HENRY'S CONSTANT
- 1.75x10(11) atm cu-m/mol (estimated) (HSDB , 2001)
- 1.73x10(-8) atm cu-m/mol @ 25 degree C (HSDB , 2001)
SPECTRAL CONSTANTS
3-12 (Organic Electronic Spectral Data, Phillips et al, John Wiley & Sons, New York) (HSDB , 2001)
OTHER/PHYSICAL
1.4758 (at 15 degrees C) (Budavari, 2000) 1.4746 (at 20 degrees C) (Budavari, 2000) 1.4730 (at 25 degrees C) (Budavari, 2000)
- NUCLEAR MAGNETIC RESONANCE
954 cP (at 25 degrees C) (HSDB , 2001) 5% Solution: 1.143 cP (at 20 degrees C) (Budavari, 2000) 10% Solution: 1.311 cP (at 20 degrees C) (Budavari, 2000) 25% Solution: 2.095 cP (at 20 degrees C) (Budavari, 2000) 50% Solution: 6.050 cP (at 20 degrees C) (Budavari, 2000) 60% Solution: 10.96 cP (at 20 degrees C) (Budavari, 2000) 70% Solution: 22.94 cP (at 20 degrees C) (Budavari, 2000) 17 cP (at 25 degrees C) (HSDB , 2001)
83% Solution: 111 cP (at 20 degrees C) (Budavari, 2000)
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