CALCIUM SULFATE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Karstenite Anhydrite Muriacite Anhydrous sulfate of lime Anhydrous gypsum CAS 7778-18-9 Calcium sulfate dihydrate CAS 10101-41-4 C.I. 77231 Precipitated calcium sulfate Native calcium sulfate Gypsum stone Alabaster Selenite Terra Alba Satinite Mineral white Satin spar Light spar Gypsum Annaline Calcium(II) Sulfate Dihydrate Land Plaster Magnesia White Satin-ite Sulfuric Acid, Calcium(2+) Salt, Dihydrate Plaster of Paris Dried calcium sulfate Dried gypsum Annalin Gypsum Hemihydrate Hemihydrate Gypsum Anhydrite Anhydrous Calcium Sulfate Anhydrous Gypsum Anhydrous Sulfate of Lime Calcium Salt of Sulfuric Acid Calcium Sulfate Calcium Sulfate (1:1) Calcium Sulphate Crysalba Drierite Gibs Karstenite Muriacite Natural Anhydrite Sulfuric Acid, Calcium Salt Sulfuric Acid, Calcium Salt (1:1) Sulfuric Acid, Calcium(2+) Salt Thiolite The hemihydrate form of calcium sulfate is most commonly referred to as plaster of Paris and the dihydrate form is generally referred to as gypsum. However, calcium sulfate dihydrate and gypsum have different Chemical Abstract Service (CAS) registry numbers. Not all references differentiate between the three major forms of calcium sulfate. Whenever possible, it is noted in this document when data apply only to a specific form. (ACGIH, 2001a; Budavari, 1996; Hathaway et al, 1996a; HSDB, 2003; Lewis, 2000; NIOSH , 1997; RTECS, 2003; Pohanish, 2002)
- CALCIUM SULFATE ANHYDROUS
Calcium sulfate dihydrate CAS 10101-41-4 C.I. 77231 Precipitated calcium sulfate Native calcium sulfate Gypsum stone Alabaster Selenite Terra Alba Satinite Mineral white Satin spar Light spar Gypsum Annaline Calcium(II) Sulfate Dihydrate Land Plaster Magnesia White Satin-ite Sulfuric Acid, Calcium(2+) Salt, Dihydrate
Plaster of Paris Dried calcium sulfate Dried gypsum Annalin Gypsum Hemihydrate Hemihydrate Gypsum
Anhydrite Anhydrous Calcium Sulfate Anhydrous Gypsum Anhydrous Sulfate of Lime Calcium Salt of Sulfuric Acid Calcium Sulfate Calcium Sulfate (1:1) Calcium Sulphate Crysalba Drierite Gibs Karstenite Muriacite Natural Anhydrite Sulfuric Acid, Calcium Salt Sulfuric Acid, Calcium Salt (1:1) Sulfuric Acid, Calcium(2+) Salt Thiolite
The hemihydrate form of calcium sulfate is most commonly referred to as plaster of Paris and the dihydrate form is generally referred to as gypsum. However, calcium sulfate dihydrate and gypsum have different Chemical Abstract Service (CAS) registry numbers. Not all references differentiate between the three major forms of calcium sulfate. Whenever possible, it is noted in this document when data apply only to a specific form.
(ACGIH, 2001a; Budavari, 1996; Hathaway et al, 1996a; HSDB, 2003; Lewis, 2000; NIOSH , 1997; RTECS, 2003; Pohanish, 2002)
IDENTIFIERS
TP 0700000 (hemihydrate) EW 4150000 (dihydrate) WS 6920000 (anhydrous)
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.
CaO4S (anhydrous) CaSO4 (anhydrous) Ca.O4S (anhydrous) Ca.H2-O4-S (anhydrous) CaH2SO4 (anhydrous) O4S.Ca.2H2O (dihydrate) CaSO4.2H2O (dihydrate) CaSO4 (O.5H2O) (hemihydrate) O4-S.Ca.1/2H2-O (hemihydrate) CaSO4.1/2 H2O (hemihydrate)
USES/FORMS/SOURCES
ANHYDRITE - Insoluble calcium sulfate is used in cement formulations and as a paper filler; soluble calcium sulfate is used as a drying agent (Budavari, 1996; Hathaway et al, 1996). (ACGIH, 2001) HEMIHYDRATE - The hemihydrate form of calcium sulfate is used for creating casts and moldings and is used in tiles, stucco, wall plaster, and wallboard (Hathaway et al, 1996a; Budavari, 1996; Ashford, 1994; ACGIH, 2001). DIHYDRATE - The dihydrate form of calcium sulfate is used in water and soil treatment, paints, enamels, paper, insecticide dusts, polishing powders, pharmaceuticals, and animal feed; in the manufacture of Portland cement, plaster of Paris, artificial marble, yeast, sulfuric acid, calcium carbide, ammonium sulfate, and polymers; and in the production of heavy chemicals. The food and pharmaceutical-grade is also used in foods as a source of calcium (Budavari, 1996; Hathaway et al, 1996a; ACGIH, 1991; Pohanish, 2002).
ANHYDRITE - The insoluble anhydrous form can be produced by completely dehydrating gypsum at above 650 degrees C. Complete dehydration of gypsum at below 300 degrees C will produce the soluble anhydrous form (Budavari, 1996; ACGIH, 2001). HEMIHYDRATE - Calcium sulfate hemihydrate can be formed from the anhydrite by absorbing 6.6% of its weight of water. It can also be formed by heating gypsum (Budavari, 1996; ACGIH, 2001a). BETA-SEMIHYDRATE is present in plaster of Paris and has a low compression strength; the temperature rise during hardening is expected to be less than with the alpha-semihydrate (Hedeboe et al, 1982). ALPHA-SEMIHYDRATE is present in dental casting materials and generates more heat (Hedeboe et al, 1982).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Calcium sulfate is irritating to the eyes, skin, and mucous membranes. Conjunctivitis, rhinitis, epistaxis, coughing, sneezing, pneumonia, and labored breathing may occur. The dental plaster form is a special form of the alpha-hemihydrate and has caused severe dermal burns. The beta-hemihydrate form does not have this property. If ingested, intestinal obstruction may occur if the material hardens, especially in the pyloric region.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. 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.
ACUTE CLINICAL EFFECTS
- The main hazard with either acute or chronic calcium sulfate exposure is from the DUST. It is an eye and respiratory tract irritant (HSDB). The probable lethal oral human dose has been estimated to be 0.5 to 5 g/kg (HSDB).
- The dental plaster form, known as Stone, is a special form of the alpha- hemihydrate. It has caused severe skin burns. Plaster of Paris, the beta-hemihydrate form, does not have this property (ACGIH, 1991).
- Formation of a gastric bezoar has been reported following ingestion of plaster consisting of 98% to 100% calcium sulfate hemihydrate. Abdominal radiographs confirmed the diagnosis. Treatment may consist of either gastric irrigation or endoscopy, or surgical intervention, depending on the time interval between plaster ingestion and presentation to the emergency department (Johari & Eskandari, 2014)t.
CHRONIC CLINICAL EFFECTS
- There is one case of exposure to an average of 194 g/m(3) intermittently over a period of 10 years producing unspecified effects on the lung (Clayton & Clayton, 1982). Pulmonary disease was not a problem in calcium sulfate miners, (Hunter, 1975).
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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 - Wash the contaminated skin with soap and water. INHALATION EXPOSURE - Move the exposed person to fresh air at once. Other measures are usually unnecessary. TARGET ORGANS - Eyes, skin and respiratory system (National Institute for Occupational Safety and Health, 2007).
GENERAL 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 Drinking glycerin, gelatin solutions, or large volumes of water may delay hardening. Surgical evaluation may be necessary if symptoms of obstruction occur.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
- Carcinogenicity Ratings for CAS7778-18-9 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Calcium sulfate 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: Calcium sulfate MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
- Carcinogenicity Ratings for CAS26499-65-0 :
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 ; Listed as: Plaster of Paris 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 CAS7778-18-9 (U.S. Environmental Protection Agency, 2011):
- EPA Risk Assessment Values for CAS26499-65-0 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS7778-18-9 (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.
- ACGIH TLV Values for CAS26499-65-0 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS7778-18-9 (AIHA, 2006):
- AIHA WEEL Values for CAS26499-65-0 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS7778-18-9 (National Institute for Occupational Safety and Health, 2007):
- NIOSH REL and IDLH Values for CAS26499-65-0 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS7778-18-9 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
Listed as: Calcium sulfate (Total dust) Table Z-1 for Calcium sulfate (Total dust): 8-hour TWA: ppm: mg/m3: 15 Ceiling Value: Skin Designation: No Notation(s): Not Listed
Listed as: Calcium sulfate (Respirable fraction) Table Z-1 for Calcium sulfate (Respirable fraction): 8-hour TWA: ppm: mg/m3: 5 Ceiling Value: Skin Designation: No Notation(s): Not Listed
- OSHA PEL Values for CAS26499-65-0 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
Listed as: Plaster of Paris (Total dust) Table Z-1 for Plaster of Paris (Total dust): 8-hour TWA: ppm: mg/m3: 15 Ceiling Value: Skin Designation: No Notation(s): Not Listed
Listed as: Plaster of Paris (Respirable fraction) Table Z-1 for Plaster of Paris (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 CAS7778-18-9 (U.S. Occupational Safety and Health Administration, 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS26499-65-0 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS7778-18-9 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS26499-65-0 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS7778-18-9 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS26499-65-0 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS7778-18-9 (U.S. Environmental Protection Agency, 2010b):
- EPA RCRA Hazardous Waste Number for CAS26499-65-0 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS7778-18-9 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS26499-65-0 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS7778-18-9 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- EPA SARA Title III, Community Right-to-Know for CAS26499-65-0 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS7778-18-9 (49 CFR 172.101 - App. B, 2005):
- DOT List of Marine Pollutants for CAS26499-65-0 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS7778-18-9 (EPA, 2005):
- EPA TSCA Inventory for CAS26499-65-0 (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 CAS7778-18-9 (NFPA, 2002):
- NFPA Hazard Ratings for CAS26499-65-0 (NFPA, 2002):
-HANDLING AND STORAGE
HANDLING
- Dust created during gypsum processing should be limited and controlled (ILO, 1983).
STORAGE
- ROOM/CABINET RECOMMENDATIONS
Keep calcium sulfate separate from diazomethane vapor, aluminum powder, and phosphorus (Lewis, 1996; Urben, 1995; NFPA, 1994).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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.
- Loose-fitting clothing made of dust-tight material, goggles, and a dust mask should be worn when working with calcium sulfate (Sittig, 1991).
EYE/FACE PROTECTION
- Safety goggles should be worn when working with calcium sulfate (Sittig, 1991).
RESPIRATORY PROTECTION
- Refer to "Recommendations for respirator selection" in the NIOSH Pocket Guide to Chemical Hazards on TOMES Plus(R) for respirator information.
- A dust mask should be worn while working with calcium sulfate (Sittig, 1991).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 7778-18-9.
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 26499-65-0.
-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 151 (ERG, 2004) Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.
Calcium sulfate is non-flammable and non-combustible. Explosion can result when it is mixed with diazomethane vapor or aluminum powder and ignition can result when it is mixed with phosphorus (NIOSH , 1997; Lewis, 1996; Urben, 1995; NFPA, 1994; Sittig, 1991).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS7778-18-9 (NFPA, 2002):
- NFPA Flammability Rating for CAS26499-65-0 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004)
Water spray, fog or regular foam. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material. Use water spray or fog; do not use straight streams.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn.
- NFPA Extinguishing Methods for CAS7778-18-9 (NFPA, 2002):
- NFPA Extinguishing Methods for CAS26499-65-0 (NFPA, 2002):
- Calcium sulfate is non-flammable (Sittig, 1991).
EXPLOSION HAZARD
- Explosion can result from an exothermic reaction when calcium sulfate is mixed with diazomethane vapor (Lewis, 1996; Urben, 1995).
- A violent or explosive reaction can occur upon heating when calcium sulfate is mixed with aluminum powder (Lewis, 1996; Urben, 1995; NFPA, 1994).
DUST/VAPOR HAZARD
- Toxic fumes of oxides of sulfur are emitted when calcium sulfate (in the anhydrous or dihydrate forms) is heated to decomposition (Lewis, 1996).
REACTIVITY HAZARD
- A violent or explosive reaction can occur upon heating when calcium sulfate is mixed with aluminum powder (Lewis, 1996; Urben, 1995).
- Explosion can result from an exothermic reaction when calcium sulfate is mixed with diazomethane vapor (Lewis, 1996; Urben, 1995).
- Calcium sulfate mixed with phosphorus will ignite at high temperatures (Lewis, 1996).
- When primed at a high temperature with a potassium nitrate-calcium silicide mixture, calcium sulfate mixed with excess red phosphorus will burn (Urben, 1995).
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 151 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 25 to 50 meters (80 to 160 feet) in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (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 151 (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.
- AIHA ERPG Values for CAS7778-18-9 (AIHA, 2006):
- AIHA ERPG Values for CAS26499-65-0 (AIHA, 2006):
- DOE TEEL Values for CAS7778-18-9 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Calcium sulfate anhydrous; (Drierite; Gypsum; Plaster of Paris TEEL-0 (units = mg/m3): 15 TEEL-1 (units = mg/m3): 30 TEEL-2 (units = mg/m3): 50 TEEL-3 (units = mg/m3): 250 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.
- DOE TEEL Values for CAS26499-65-0 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS7778-18-9 (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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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):
- AEGL Values for CAS26499-65-0 (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; 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; 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, 2007; 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, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; 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, 2008; 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, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; 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, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; 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, 2008; 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, 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 CAS7778-18-9 (National Institute for Occupational Safety and Health, 2007):
- NIOSH IDLH Values for CAS26499-65-0 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 151 (ERG, 2004) 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. Cover with plastic sheet to prevent spreading. 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 151 (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.
When cleaning up a spill, wear protective clothing and equipment. Vacuum spill or use other methods which avoid raising dust (Sittig, 1991).
Landfilling is the suggested disposal method (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
- No information found at the time of this review.
ABIOTIC DEGRADATION
- No information found at the time of this review.
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- ANHYDRITE: The pure anhydrous form of calcium sulfate is hygroscopic and exists as a colorless or white powder or as varied colored, odorless orthorhombic crystals (Budavari, 1996; Lewis, 1996; ACGIH, 2001). Due to its high affinity for water, the soluble anhydrite will absorb 6.6% of its weight of water and thus form the stable hemihydrate(HSDB, 2003).
- HEMIHYDRATE: Calcium sulfate hemihydrate is a white or yellowish, finely divided, powder that is odorless and tasteless and loses water when heated above 163 degrees C(NIOSH, 2003; Budavari, 1996; Ashford, 1994; ACGIH, 2001).
- DIHYDRATE: The dihydrate form occurs in colorless, monoclinic, hygroscopic crystals or in lumps or powder (Budavari, 1996; Lewis, 2000).
VAPOR PRESSURE
- 0 mmHg (approximate) (NIOSH, 2005)
DENSITY
- TEMPERATURE AND/OR PRESSURE NOT LISTED
ANHYDRITE: 2.96 g/mL (Budavari, 1996) ANHYDRITE: 2.964 g/mL(Lewis, 2000) DIHYDRATE: 2.32 g/mL (Budavari, 1996; Lewis, 2000)
FREEZING/MELTING POINT
ANHYDRITE 1570 degrees C (Lewis, 1996) 1450 degrees C (Sittig, 1991; Lewis, 1997) 1360 degrees C (decomposes) (ACGIH, 1991) 2840 degrees F (decomposes) (NIOSH, 2005)
HEMIHYDRATE 163 degrees C (loses 1/2 H2O) (ACGIH, 1991) 325 degrees F (loses H20) (NIOSH , 1999)
DIHYDRATE 128 degrees C (loses 1 1/2 H2O) (Lewis, 1996; ACGIH, 1991) 163 degrees C (loses 2H2O) (ACGIH, 1991)
BOILING POINT
- ANHYDRITE: decomposes (NIOSH, 2005)
- DIHYDRATE: 163 degrees C (Lewis, 1996)
EXPLOSIVE LIMITS
SOLUBILITY
Anhydrite: Calcium sulfate is slightly soluble in water(Lewis, 2000). Anhydrite: 0.20 g in 100 g water (at 25 degrees C) (ACGIH, 2001) Anhydrite: 0.2 pts/100 pts (at 18.75 degrees) (Budavari, 1996) Anhydrite: 0.27 g/100 g (at 20 degrees C) (HSDB, 2003) Anhydrite: 0.3% (percent by weight) (NIOSH, 2003) Hemihydrate: The hemihydrate form slightly soluble in hot water (HSDB, 2003) Hemihydrate: 3.0 g/L (at 25 degrees C) (Ashford, 1994) Hemihydrate: 0.30 g in 100 g water (at 25 degrees C) (ACGIH, 2001) Hemihydrate: 0.3 g/100 cc water (at 20 degrees C) (HSDB, 2003) Hemihydrate: 0.67 g/100 g (at 20 degrees C) (alpha-form) (HSDB, 2003) Hemihydrate: 0.88 g/100 g (at 20 degrees C) (beta-form) (HSDB, 2003) Hemihydrate: 0.209 g/100 cc (at 30 degrees C) (HSDB, 2003) Hemihydrate: 0.1619 g/100 cc (at 100 degrees C) (HSDB, 2003) Dihydrate: The dihydrate form of calcium sulfate is soluble or slightly soluble in water (Budavari, 1996; Lewis, 2000). Dihydrate: 0.24 g in 100 g water (at 25 degrees C) (ACGIH, 2001) Dihydrate: 0.21 g/100 g (at 20 degrees C) (HSDB, 2003)
Anhydrite: Calcium sulfate dissolves in acids. The soluble anhydrite is soluble in sodium thiosulfate (HSDB , 1999; Lewis, 1996). Hemihydrate: The hemihydrate form is soluble in glycerin, ammonium salts, and acids (HSDB , 1999). DIHYDRATE
OTHER/PHYSICAL
ANHYDRITE (SOLUBLE): 1.505, 1.548 (HSDB , 1999) DIHYDRATE: 1.520, 1.525, 1.530 (HSDB , 1999)
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