CHROMIUM (III)
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
CHROMIC ION CHROMIUM (3+) CHROMIUM (III) CHROMIUM (III) CATION CHROMIUM (III) COMPOUNDS CHROMIUM (III) ION CHROMIUM ION (3+) CHROMIUM ION (Cr3+) CHROMIUM [TRIVALENT] 16065-83-1 CAS
IDENTIFIERS
SYNONYM REFERENCE
- (IARC, 1997;(Lewis, 2000)RTECS, 2001
USES/FORMS/SOURCES
Trivalent chromium promotes metabolism of glucose, fat, and protein by facilitating the action of insulin in humans and animals. Chromium (III) deficiency can cause impaired glucose metabolism and increased risk of cardiovascular disease (Leung, 1995; Clayton & Clayton, 1994). Chromium in the +3 oxidation state {Cr(III)} is a trace element that is used by body builders to enhance glucose utilization and increase lean body mass (Katz & Salem, 1993; Ellenhorn et al, 1997). The National Research Council recommends a daily allowance of 50 to 200 mcg. Men given 200 mcg Cr (III)/day while enlisted in a daily weight training program increased their lean body mass (ATSDR, 1993; (Clayton & Clayton, 1994). Trivalent chromium compounds are used to make pigments and in the leather tanning process (ATSDR, 1993). Chromium compounds are used medically in astringents and antiseptics (HSDB , 2001).
Chromic compounds, Cr (III), are stable and form many commercially used compounds. These include chromic oxide and chromium sulfate (ILO, 1998). Chromic oxide, a trivalent chromium compound, is the most important chromium compound. It is used as a pigment and is also known as chromic oxide green (Clayton & Clayton, 1994). Trivalent chromium compounds resemble aluminum (+3) compounds (Clayton & Clayton, 1994). Trivalent salts can be found in enamel used in the manufacture of kitchen ranges. During the manufacturing process at one plant, the trivalent salts were discovered to convert to hexavalent salts when in contact with the hooks carrying the ranges during the baking process and subsequently caused an outbreak of hand ulceration among workers (Deng et al, 1990).
Chromium can be found in foods. Brewer's yeast, beer, oysters, mushrooms and meats (especially kidney) are good sources of chromium. Some researchers have suggested that low serum levels of chromium may be due to diets high in processed or refined foods. Trivalent chromium naturally exists in the environment. It is also the most abundant form of chromium in the environment (Clayton & Clayton, 1994). Normally, trivalent chromium is found as free ionized, protein bound (mainly transferrin), or as a component of the glucose tolerance factor (GTF, Cr-nicotinic acid-amino acid complex) (Leung, 1995).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Chromium in the +3 oxidation state [Cr(III)] is a trace element that is used by body builders to enhance glucose utilization and increase lean body mass. The National Research Council recommends a daily allowance of 50 to 200 mcg. Trivalent chromium compounds are used to make pigments and in the leather tanning process. Chromium compounds are used medically in astringents and antiseptics.
- PHARMACOLOGY: Trivalent chromium is an essential nutrient that promotes metabolism of glucose, fat, and protein by facilitating the action of insulin in humans and animals. Chromium (III) deficiency can cause impaired glucose metabolism and increased risk of cardiovascular disease. Chromium deficiency has been observed in protein-calorie malnutrition and in patients receiving total parenteral nutrition (TPN) lacking in chromium supplementation.
- EPIDEMIOLOGY: Exposure is common, but serious toxicity is rare.
Chromium metal is relatively nontoxic. There is little evidence of substantial toxicity from chromic salts (trivalent chromium), probably because of poor skin and mucous membrane penetration. Trivalent chromium compounds are considered less toxic than hexavalent chromium compounds. It is considered an irritant and contact dermatitis has been reported with exposure. Long-term exposure to chromium may cause chronic bronchitis, sinusitis, rhinitis, asthma, and a type of pneumoconiosis. The sweat-gland lesions that appear after exposure to hexavalent chromium may result from its reduction to trivalent chromium after absorption, and subsequent formation of antigen-antibody complexes. Hexavalent chromium and the supplement chromium picolinate are covered in separate managements. Refer to "CHROMIUM, HEXAVALENT" and "CHROMIUM, PICOLINATE" managements for further information.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
ORAL 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.
DERMAL EXPOSURE Wash the exposed area with water for 15 minutes. A physician may need to examine the exposed area if irritation or pain persists. Some authors have recommended dermal irrigation for 15 minutes with a 10% ascorbic acid solution for hexavalent chromium decontamination. Ascorbic acid will reduce the more toxic chromium (VI) to the less toxic chromium (III) ion (Bradberry & Vale, 1999; Milner, 1980; Korallus et al, 1984). Unless a mixed exposure, there is no proven benefit to the use of ascorbic acid for chromium (III) compound decontamination.
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.
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
Exposure to trivalent chromium appears to be less toxic than hexavalent chromium (Katz & Salem, 1993; Haddad et al, 1998). It has been estimated that hexavalent chromium compounds are 10 to 100 times more toxic than trivalent compounds by the oral route (Katz & Salem, 1993).
- Carcinogenicity Ratings for CAS16065-83-1 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A1 ; Listed as: Chromite ore processing (Chromate), as Cr EPA (U.S. Environmental Protection Agency, 2011): D ; Listed as: Chromium(III), insoluble salts 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): 3 ; Listed as: Chromium III compounds 3 : The agent (mixture or exposure circumstance) is not classifiable as to its carcinogenicity to humans. This category is used most commonly for agents, mixtures and exposure circumstances for which the evidence of carcinogenicity is inadequate in humans and inadequate or limited in experimental animals. Exceptionally, agents (mixtures) for which the evidence of carcinogenicity is inadequate in humans but sufficient in experimental animals may be placed in this category when there is strong evidence that the mechanism of carcinogenicity in experimental animals does not operate in humans. Agents, mixtures and exposure circumstances that do not fall into any other group are also placed in this category.
NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Chromium(III) compounds (as Cr) 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 CAS16065-83-1 (U.S. Environmental Protection Agency, 2011):
Oral: Slope Factor: RfD: 1.5 mg/kg-day
Inhalation: Drinking Water:
References: (ATSDR, 1993; NIOSH, 1996. Values are from ATSDR, 1993, unless otherwise noted.
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS16065-83-1 (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 CAS16065-83-1 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS16065-83-1 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS16065-83-1 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS16065-83-1 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS16065-83-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS16065-83-1 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS16065-83-1 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS16065-83-1 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS16065-83-1 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS16065-83-1 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS16065-83-1 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS16065-83-1 (NFPA, 2002):
-HANDLING AND STORAGE
STORAGE
Chromium should be handled, used and stored in areas that are clearly marked and regulated. It should be stored separately from strong oxidizers such as bromine, chlorine, and fluorine. Ignition sources should be prohibited in chromium storage areas (Sittig, 1991).
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
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 16065-83-1.
ENGINEERING CONTROLS
- Dusts and mists containing chromium should be controlled in the workplace. Specially designed exhaust ventilation is an example of one control method. Use of wet methods for cleaning is another way to prevent dusts and mists from circulating in the air (ILO, 1998).
- Process enclosure is recommended for tasks that use corrosion inhibiting and coloring pigments, color blending, artists' colors, inks, rubber, ceramics, and jointing pastes (NIOSH, 1978).
- The EPA regulates emissions from chromium electroplating and anodizing tanks. Emissions from these tanks can be reduced by using one of the following methods: packed bed scrubber, composite mesh-pad system, fume suppressants, or fume suppressants that contain a wetting agent. Choice of method depends on size and type of plating or anodizing tank (EPA, 1995).
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS16065-83-1 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS16065-83-1 (NFPA, 2002):
DUST/VAPOR HAZARD
- When compounds containing chromium (III) are heated to decomposition, they release chromium vapor (Lewis, 2000).
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS16065-83-1 (AIHA, 2006):
- DOE TEEL Values for CAS16065-83-1 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS16065-83-1 (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 CAS16065-83-1 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
Chromium wastes from plating, tanning, and chemical plants can be recovered and recycled. Cooling tower blow-down water can also be recycled (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.
Cr (III) may be converted into a hydrous oxide using lime or caustic soda (ATSDR, 1993). The trivalent form of chromium may be treated by hydroxide precipitation using either calcium hydroxide (lime) or sodium hydroxide (caustic) as the precipitant. Trivalent chromium in mixed waste solutions containing divalent and monovalent cations may be selectively removed by phosphate precipitation (Freeman, 1989). Activated carbon was found to adsorb trivalent chromium in aqueous solutions. The pH of the solution was critical, with the maximum adsorption occurring at pH 5. Temperature also affected the adsorption capacity; 20% more chromium was absorbed at 40 degrees C than at 25 degrees C (Leyvaramos et al, 1995). Chromium (III) in pretreated sludge may be buried on land or dumped in the ocean (ATSDR, 1993).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- To protect freshwater aquatic life, trivalent chromium should not exceed exp (1.08 ln (hardness) + 3.48) mcg/L. Based on acute toxicity, protection of saltwater aquatic life requires a limit of 10,300 mcg/L. A level of 170 mcg/L, or less, in water will protect humans (Sittig, 1991).
- Although pipes for carrying water often contain significant chromium levels, little leaching occurs. However, trivalent chromium in drinking water can be oxidized to the hexavalent state during chlorination (HSDB , 2001).
ENVIRONMENTAL FATE AND KINETICS
Chromium (III) salts, except Cr2O3, may undergo an unlikely atmospheric reaction in the presence of 1% manganese oxide to form Cr (VI) (ATSDR, 1993).
SURFACE WATER Trivalent chromium may be oxidized to Cr (VI) in lake water, with an estimated half-life of 9 years. Addition of manganese oxide to this process decreased the oxidation half-life to about 2 years. This oxidation process is insignificant in natural waters (ATSDR, 1993). Cr (III) compounds will predominate in acidic water, and under reducing conditions such as those found in deep groundwaters (ATSDR, 1993). U.S. drinking water supplies contain an average of 1.8 mcg Cr (III)/L, with a range of 0.4 - 8.0 mcg Cr (III)/L (ATSDR, 1993). Trivalent chromium may adsorb onto clays or organic materials or iron oxide in water. Hexavalent chromium is expected to be reduced to the trivalent form by organic materials. Chromium will not volatilize from surface water (ATSDR, 1993).
TERRESTRIAL Trivalent chromium is usually in insoluble carbonate or chromium (III) oxide form in soil. These forms are not mobile in soil. However, Cr (III) may form soluble complexes with soil organic matter, especially in low pH soils. Organic complexes of Cr (III) would be mobile in soil (ATSDR, 1993). Soil adsorption coefficients (Kds) for chromium (III) range from 470 to 150,000 mL/g (Dragun, 1988). Soluble and unadsorbed trivalent and hexavalent complexes may leach into groundwater. The leaching potential of hexavalent chromium increases with higher soil pH, while lower pH from acid rain increases the likelihood of leaching by acid-soluble trivalent and hexavalent chromium compounds (ATSDR, 1993).
OTHER Trivalent chromium added to lake water showed a slow oxidation to the hexavalent form, with an oxidation half-life of 9 years. Adding 50 mg/L manganese oxide reduced the half-life to approximately 2 years (ATSDR, 1993).
BIOACCUMULATION
ENVIRONMENTAL TOXICITY
- Values are from OHM/TADS (2001):
IL50 - (MULTIPLE) EURASION WATERMILFOIL: 9.9 ppm - root weight affected IL50 - (MULTIPLE) EURASION WATERMILFOIL: 14.6 ppm - stem weight affected IL50 - (MULTIPLE) EURASION WATERMILFOIL: 24.4 ppm - root length affected IL50 - (MULTIPLE) EURASION WATERMILFOIL: 26 ppm - stem length affected
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Trivalent chromium compounds are amphoteric (Clayton & Clayton, 1994). The majority of trivalent chromium compounds are insoluble in water. Exceptions include acetate, nitrate, and chromium (III) chloride-hexahydrate salts (ATSDR, 1993).
SOLUBILITY
The majority of trivalent chromium compounds are insoluble in water. Exceptions include acetate, nitrate, and chromium (III) chloride-hexahydrate salts (ATSDR, 1993).
-REFERENCES
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