MOLYBDENUM
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Molybdate Molecular Formula: Mo MCHVL TSM1 CAS 7439-48-7 (metal) NIOSH/RTECS QA 4680000 Ammonium molybdate Molybdic acid, diammonium salt Diammonium molybdate Molecular Formula: (NH4)2MoO4 CAS 13106-76-8 NIOSH/RTECS QA 4900000 Molybdic acid, commercial Molecular Formula: (NH4)6Mo7O24.4H2O Molecular Formula: CaMoO4 Molybdenum orange Molybdenum-lead chromate C.I. pigment red 104 Wulfenite Lead chromate, sulfate and molybdate CAS 12709-98-7 NIOSH/RTECS OG 1625000 Chrome vermillion C.I. pigment red 104 Mineral fire red 5DDS Mineral fire red 5GS Molybdate red Molybdenum red Molybden red NCI-c 54626 CAS 12656-85-8 NIOSH/RTECS QA 4660000 Molybdenum dichloride Molecular Formula: MoCl2 Molybdic sulfide Molybdenum glance Natural molybdenite Molybdenite Molykote Mopolm Molecular Formula: MoS2 NIOSH/RTECS QA 4697000 Molecular Formula: MoCl5 CAS 10241-05-1 NIOSH/RTECS QA 4690000 Molybdic anhydride Molybdic trioxide Molybdenum anhydride Molybdenum (VI) oxide Molybdic oxide Molybdic acid anhydride Molybdite Natural molybdite Molecular Formula: MoO3 CAS 1313-27-5 NIOSH/RTECS QA 4725000 Molecular Formula: H2MoO4 CAS 7782-91-4 Molybdic acid, disodium salt Molecular Formula: Na2MoO4 Disodium molybdate dihydrate Molecular Formula: Na2MoO4.(H2O)2 CAS 10102-40-6
Molybdate Molecular Formula: Mo MCHVL TSM1 CAS 7439-48-7 (metal) NIOSH/RTECS QA 4680000
Chrome vermillion C.I. pigment red 104 Mineral fire red 5DDS Mineral fire red 5GS Molybdate red Molybdenum red Molybden red NCI-c 54626 CAS 12656-85-8 NIOSH/RTECS QA 4660000
Molybdenum dichloride Molecular Formula: MoCl2
Molybdic sulfide Molybdenum glance Natural molybdenite Molybdenite Molykote Mopolm Molecular Formula: MoS2 NIOSH/RTECS QA 4697000
Molecular Formula: MoCl5 CAS 10241-05-1 NIOSH/RTECS QA 4690000
Molybdic anhydride Molybdic trioxide Molybdenum anhydride Molybdenum (VI) oxide Molybdic oxide Molybdic acid anhydride Molybdite Natural molybdite Molecular Formula: MoO3 CAS 1313-27-5 NIOSH/RTECS QA 4725000
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.
USES/FORMS/SOURCES
Molybdenum is an essential trace element for humans and mammals. The main commercial source is molybdenite (MoS2) (Tallkvist & Oskarsson, 2015; International Molybdenum Association (IMOA), 2013). Molybdenum compounds (Mo, MoO3, MoS2) are used for a variety of applications. They are used as catalysts, in ceramics, labeling glass containers, fertilizers as a trace element, electroplating, and the tanning of skins (Langard, 2001). Molybdenum inorganic and organic complexes are used for color (pigments, insoluble dyes, mordants) (Langard, 2001). Molybdenum metal is used for electronic parts. Molybdenum steel is used in the manufacture of parts for missiles and aircraft (Langard, 2001). MOLYBDENUM ACETLYACETONATE is a catalyst for the polymerization of ethylene and the production of polyurethane foam (Barceloux, 1999). MOLYBDENUM DISULFIDE (molybdenite) is used as a lubricant which does not require a water film for lubrication and can therefore be used in a vacuum (Langard, 2001). AMMONIUM TETRATHIOMOLYBDATE has been used an experimental copper chelating agent for the treatment of Wilson's disease (Barceloux, 1999). MOLYBDENUM TRIOXIDE is used as a corrosion inhibitor and a reagent for chemical analysis (Barceloux, 1999). ZINC MOLYBDATE is used as a stabilizer and anticorrosive in paint (Barceloux, 1999). FERTILIZERS: Standard commercial fertilizers contain 2 to 6 ppm molybdenum (Barceloux, 1999).
SOLUBLE COMPOUNDS Sodium molybdate, ammonium dimolybdate, and ammonium heptamolybdate are highly soluble molybdenum salts (solubility greater than 100 mg/L). These compounds will dissociate into the molybdate anion [MoO4]2- under physiological conditions. Molybdenum is taken up into organisms and is present in blood as molybdate. Molybdenum trioxide, a moderately soluble compound, reacts with water under acidification to molybdate anions (International Molybdenum Association (IMOA), 2013; Hathaway et al, 1996). These compounds are readily absorbed from the gastrointestinal tract (Friberg et al, 1986).
INSOLUBLE COMPOUNDS Calcium molybdate, molybdenum halides, molybdenum disulfide, molybdenum dioxide are insoluble compounds (Hathaway et al, 1996).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Molybdenum is an essential trace element for humans and mammals. The main commercial source is molybdenite (MoS2). Molybdenum compounds (Mo, MoO3, MoS2) are used as catalysts, lubricants (molybdenum disulfide), corrosion inhibitors (molybdenum trioxide), and stabilizers (zinc molybdate). They are also used in ceramics, labeling glass containers, fertilizers as a trace element, and electroplating. Molybdenum metal is used for electronic parts and molybdenum steel is used in the manufacture of parts for missiles and aircraft. Molybdenum inorganic and organic complexes are used for color (pigments, insoluble dyes, mordants).
- TOXICOLOGY: Sodium molybdate, ammonium dimolybdate, and ammonium heptamolybdate are highly soluble molybdenum salts. Other soluble molybdenum include ammonium molybdate and molybdenum trioxide. Soluble molybdenum compounds are readily absorbed from the gastrointestinal tract. Calcium molybdate, molybdenum halides, molybdenum disulfide, molybdenum dioxide are insoluble compounds. The main routes of exposure are via inhalation and dermal contact. Since dermal absorption is negligible, inhalational exposure is the main concern. There seems to be a reciprocal relationship between molybdenum and copper. In ruminants (especially cattle and sheep), intake of herbage with a high molybdenum content produces "scouring" disease (diarrhea). A copper deficiency aggravates this disease and administration of copper salts alleviates the disease. Evidence suggests that excess molybdenum promotes binding of copper to a serum protein, thus limiting uptakes of copper in tissue. Molybdenum is a cofactor of xanthine oxidase. Excess molybdenum may induce xanthine oxidase.
- EPIDEMIOLOGY: Exposure to molybdenum is common. Trace amounts of soluble molybdate can be found in foods and drinking water. Mineral supplements can also contain trace amounts of sodium molybdate and ammonium dimolybdate. Occupational exposure to molybdenum from mining operations and industrial sources have also been reported.
There are few reports of human toxicity. Toxicity information is mostly based on animal data. Molybdenum can produce mild eye, nose, throat, and skin irritations. Elevated liver enzymes, diarrhea, weakness, fatigue, anorexia, headache, joint and muscle pain, tremor, pneumoconiosis, and/or chest pain have been reported in workers exposed to molybdenum. Pancytopenia was reported in 2 patients who received copper chelator tetrathiomolybdate. High dietary intake of molybdenum may alter copper balance, increase serum ceruloplasmin, and theoretically predispose some individuals to anemia. Hypothyroidism may also occur. Molybdenum toxicity is associated with copper and sulfate deficiency in animals. Diarrhea, anorexia, listlessness, fatty degeneration of the liver, dystrophic changes and kidney cell swelling, and anemia have been reported in animals.
- 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
TOXICOLOGY: Sodium molybdate, ammonium dimolybdate, and ammonium heptamolybdate are highly soluble molybdenum salts. Other soluble molybdenum compounds include ammonium molybdate and molybdenum trioxide. Soluble molybdenum compounds are readily absorbed from the gastrointestinal tract. Calcium molybdate, molybdenum halides, molybdenum disulfide, molybdenum dioxide are insoluble compounds. The main routes of exposure are via inhalation and dermal contact. Since dermal absorption is negligible, inhalational exposure is the main concern. There seems to be a reciprocal relationship between molybdenum and copper. In ruminants (especially cattle and sheep), intake of herbage with a high molybdenum content produces "scouring" disease (diarrhea). A copper deficiency aggravates this disease and administration of copper salts alleviates the disease. Evidence suggests that excess molybdenum promotes binding of copper to a serum protein, thus limiting uptakes of copper in tissue. Molybdenum is a cofactor of xanthine oxidase. Excess molybdenum may induce xanthine oxidase. EPIDEMIOLOGY: Exposure to molybdenum is common. Trace amounts of soluble molybdate can be found in foods and drinking water. Mineral supplements can also contain trace amounts of sodium molybdate and ammonium dimolybdate. Occupational exposure to molybdenum from mining operations and industrial sources have also been reported. TOXICITY: There are few reports of human toxicity. Toxicity information is mostly based on animal data. Molybdenum can produce mild eye, nose, throat, and skin irritations. Elevated liver enzymes, diarrhea, weakness, fatigue, anorexia, headache, joint and muscle pain, tremor, pneumoconiosis, and/or chest pain have been reported in workers exposed to molybdenum. Pancytopenia was reported in 2 patients who received copper chelator tetrathiomolybdate. High dietary intake of molybdenum may alter copper balance, increase serum ceruloplasmin, and theoretically predispose some individuals to anemia. Hypothyroidism may also occur. Molybdenum toxicity is associated with copper and sulfate deficiency in animals. Diarrhea, anorexia, listlessness, fatty degeneration of the liver, dystrophic changes and kidney cell swelling, and anemia have been reported in animals.
Molybdenum can produce mild eye, nose, throat, and skin irritations (Occupational Safety & Health Administration (OSHA), 2012).
CASE SERIES: Pancytopenia resulted in 2 patients receiving the copper chelator tetrathiomolybdate (Harper & Walshe, 1986). ANEMIA: Data in humans suggests that high dietary molybdenum potentially can produce mineral imbalances (e.g. copper deficiency) which may predispose some individuals to hypochromic microcytic anemia (IRIS , 1995).
Evidence suggests that molybdenum may produce liver dysfunction. Workmen in Russia Mo-Cu plant reported a fall in A/G ratios due to a rise in globulins, primarily alpha-globulins that has been interpreted as evidence of liver dysfunction (Stokinger, 1982).
Molybdenum is a cofactor for xanthine oxidase and aldehyde oxidase and is necessary for purine metabolism. Excess intake of molybdenum stimulates xanthine oxidase producing elevated blood and urine levels of uric acid which may predispose toward the development of gout (Langard, 2001; Hazardous Substances Databank (HSDB), 2010).
Weakness, fatigue, anorexia, headache, joint and muscle pain and hand tremor were reported in USSR miners and metallurgy workers chronically exposed to 60 to 600 mg/m(3) (Lener & Bibr, 1984; Hathaway et al, 1996; Hazardous Substances Databank (HSDB), 2010).
Molybdenum exposure can produce respiratory irritation (Hazardous Substances Databank (HSDB), 2010). Dry cough and chest pains may develop after chronic industrial exposure to 1 to 19 mg/m(3) metallic molybdenum and molybdenum oxides (Lener & Bibr, 1984; Hazardous Substances Databank (HSDB), 2010).
CHRONIC CLINICAL EFFECTS
- Occupational exposure in a molybdenum roasting plant produced subjective complaints of joint pains, head- and backaches, and nonspecific changes in hair and skin (Friberg et al, 1986). Chronic occupational exposure to molybdenum and/or molybdenum trioxide has resulted in pneumoconiosis (Hazardous Substances Databank (HSDB), 2010).
- Persons living in regions with high molybdenum AND low copper have developed a gout-like condition and deformities in the joints (Friberg et al, 1986). This may be explained by higher levels of xanthine oxidase, which is an enzyme in the production of uric acid (Friberg et al, 1986).
- Molybdenum poisoning has occurred in livestock, also in areas with high molybdenum and low copper levels. Livestock have developed anemia, gastrointestinal disturbances, and abnormal bone growth (Friberg et al, 1986).
- Molybdenum has caused liver, kidney, and spleen damage, bone deformities during growth, anemia, and growth retardation in chronically exposed laboratory animals (Friberg et al, 1986).
- Molybdenum (in the form of sodium molybdate or thiomolybdate) given to guinea pigs in the drinking water reduced liver copper and elevated plasma copper levels; damage to the pancreas was thought to be the result of copper deficiency, rather than from direct molybdenum toxicity (Howell et al, 1993). Molybdenum was a contact irritant in mice when applied as the chloride salt, but did cause dermal sensitization or produce changes in multiple immunological parameters (Abdouh et al, 1995).
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
DILUTION: If no respiratory compromise is present, administer milk or water as soon as possible after ingestion. Dilution may only be helpful if performed in the first seconds to minutes after ingestion. The ideal amount is unknown; no more than 8 ounces (240 mL) in adults and 4 ounces (120 mL) in children is recommended to minimize the risk of vomiting.
- EYE/DERMAL EXPOSURE: Molybdenum can produce mild eye, nose, throat, and skin irritations. Flush eyes with copious amounts of water. Skin should be thoroughly irrigated. Contact dermatitis may arise after repeated exposure to irritants.
-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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
Injected molybdenum produced death in 2 to 4 days in guinea pigs, depending on the dose given (Stokinger, 1982). Lethal doses of molybdenum and its salts by oral or parenteral exposure are above 100 mg/kg in the animal species tested. Intratracheal instillation would be expected to possess a lower lethal dose (molybdenum powder LDLo was 70 mg/kg in the rabbit; (Friberg L, Boston P & Nordberg G et al, 1975).
MAXIMUM TOLERATED EXPOSURE
Industrial toxicology reports indicate that in general molybdenum compounds exhibit a low order of toxicity. The trioxide and ammonium molybdate are generally more toxic than the ore (molybdenite), the metal, molybdenum disulfide or molybdenum dioxide (ACGIH, 1991; Stokinger, 1982; ACGIH, 1991).
A LOAEL (Lowest Observable Adverse Effect Level) has been designated as 0.14 mg/kg/day in adults, based on long term exposure. A NOAEL (No Observable Adverse Effect Level) for adults has been reported as 4 mcg/kg/day to 8 mcg/kg/day (IRIS , 1995) or 22 to 1500 mcg/day (Turnlund et al, 1995). SODIUM MOLYBDATE DIHYDRATE: In a 90-day oral repeated-dose toxicity study, rats were administered 5, 17, or 60 mg/kg/day of sodium molybdate dihydrate. Reduced body weight gains and kidney effects (slight diffuse hyperplasia of the proximal tubules) were observed only following 60 mg/kg/day dose. The NOAEL for this dose was 17 mg Mo/kg/day (International Molybdenum Association (IMOA), 2013). CASE REPORT: A man developed anxiety, agitation, visual and auditory hallucination, excessive craving for salt, insomnia, diarrhea, and painful and cold extremities after taking an average of 7 to 8 molybdenum tablets per day for 18 days (total cumulative dose: 13.5 mg). On day 22, he developed petit mal seizures and became suicidal. His condition deteriorated further and he developed coma after receiving medications for a grand mal seizure. His blood molybdenum concentration was 7.7 ng/mL on day 25 and 1.7 ng/mL about 6 weeks after starting molybdenum supplements. Treatment with chelation therapy (calcium ethylene diamine tetraacetic acid (CaEDTA)) improved his symptoms; however neuropsychological tests and Spectral Emission Computer Tomography images (SPECT) revealed frontal cortical damage of the brain. A year later, he was diagnosed with toxic encephalopathy, learning disability, major depression, and post-traumatic stress disorder (Momcilovic, 1999). A causal relationship could not be established.
NIOSH Immediately Dangerous to Life or Health (IDLH) concentration (NIOSH , 1996; Hazardous Substances Databank (HSDB), 2010): MOLYBDENUM METAL: 5000 mg/m(3), as molybdenum (Occupational Safety & Health Administration (OSHA), 2012) SOLUBLE MOLYBDENUM COMPOUNDS: 1000 mg/m(3), as molybdenum (NIOSH , 1996).
Threshold Limit Value-Time-Weighted Average (TLV-TWA) = 10 mg/m(3) (inhalable particulate mass) and 3 mg/m(3) (respirable particulate mass); mild eye, nose, throat, and skin irritation (Hazardous Substances Databank (HSDB), 2010; Occupational Safety & Health Administration (OSHA), 2012). MOLYBDENUM TRIOXIDE: In a 13-week inhalation toxicity study, animals were exposed to 0, 1, 3, 10, 30, and 100 mg MoO3/m(3) for 6.5 hours/day, 5 days/week for 13 weeks. No treatment-related effects were observed at all concentrations. A true NOAEC (No Observed Adverse Effect Concentration) was determined to be 100 mg MoO3/m(3) (corresponding to 66.7 mg Mo/m(3). In 2-year inhalation studies, animals received 0, 10, 30, and 100 mg MoO3/m(3) of molybdenum trioxide. Although no adverse effects were observed, significant increases in liver copper concentrations were observed following exposure to 30 mg/m(3) and 100 mg/m(3). A NOAEC of 100 mg MoO3/m(3) (corresponding to 66.7 mg Mo/m(3)) and a NOEC (No Observed Effect Concentration) of 10 mg MoO3/m(3) (corresponding to 6.7 mg Mo/m(3)) were observed (International Molybdenum Association (IMOA), 2013). MOLYBDENUM TRIOXIDE: In repeated-dose animal toxicity studies, molybdate blood concentrations in rats following the inhalation of 100 mg/m(3) molybdenum trioxide (67 mg Mo/m(3)) were similar to those resulting from dietary exposure to 17 to 20 mg Mo/kg body weight/day (in the form of sodium molybdate in the diet) (International Molybdenum Association (IMOA), 2013).
MOLYBDENUM DISULFIDE & MOLYBDENUM METAL: Molybdenum disulfide by oral exposure or inhalation was found to be relatively non-toxic in animals. Rats showed no toxicity while ingesting up to 500 mg daily for 44 days. Increased respiration was observed in guinea pigs inhaling 286 mg/m(3) Mo for 1 hour daily 5 days weekly for 5 weeks. Daily IP injection produced 17% mortality in 4 days and 25% mortality in 4 months in guinea pigs at a daily dosage of 800 mg/kg. Survivors gained weight and remained well (Fairhall LT, Dunn RC & Sharpless NE et al, 1945). MOLYBDENUM OXIDES/METAL DUSTS MoO3 dust by inhalation exposure for 1 hour daily at 205 mg Mo/m(3) in guinea pigs was extremely irritating. Anorexia and weight loss, diarrhea, muscular incoordination as well as loss of hair was reported. Death occurred in 26 of 51 (51%) animals. Freshly generated MoO3 fume (190 mg/m(3) Mo) was found to be less toxic under the same exposure conditions, with only 8.3% mortality. No mortality occurred when exposure was decreased to 53 mg Mo/m(3) (Fairhall LT, Dunn RC & Sharpless NE et al, 1945). Under conditions as MoO3 dust, 20.8% mortality occurred (N=24 guinea pigs) for CaMoO4 dust at 159 mg Mo/m(3) without showing any toxic signs (Fairhall LT, Dunn RC & Sharpless NE et al, 1945). No toxic effects were seen in rats after a single inhalation exposure to 3 to 30 g/m(3) metallic molybdenum or Mo compounds. A single intratracheal dose of 50 mg Mo or MoO3 suspension produced emphysema, interstitial fibrosis and regional lymph node changes in rats. Similarly exposed rabbits showed diffuse pneumoconiosis and interstitial pneumonitis several months later (Lener & Bibr, 1984).
CALCIUM & ZINC MOLYBDATES: Acute toxicity tests in laboratory animals showed Ca and Zn molybdates were "practically nontoxic" orally, percutaneously, and by inhalation according to the definition of the Federal Hazardous Substance Labeling Act for purposes of labeling for Climax Molybdenum between 1957 and 1963. No skin or eye irritation was found (Stokinger, 1982). HEXAVALENT MO/AMMONIUM MO/DIHYDRATE MO SALT: Hexavalent compounds given orally to rats produced an LD50 of 101 mg/kg for CaMoO4, 125 mg/kg for MoO3 and 333 mg/kg for (NH4)2MoO4 (Fairhall LT, Dunn RC & Sharpless NE et al, 1945). Ammonium molybdate (25 mg/kg) added to rat feed for 100 days had little effect whereas 50 mg/kg slightly decreased weight gain. The dihydrate salt (Na2MoO4(2H2O)) fed to rabbits in the diet at 0.1% and higher was uniformly fatal within weeks. When copper was added to this diet, toxicity was prevented (Stokinger, 1982).
- Carcinogenicity Ratings for CAS7439-98-7 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): A3 ; Listed as: Molybdenum, as Mo; soluble compounds A3 :Confirmed Animal Carcinogen with Unknown Relevance to Humans: The agent is carcinogenic in experimental animals at a relatively high dose, by route(s) of administration, at site(s), of histologic type(s), or by mechanism(s) that may not be relevant to worker exposure. Available epidemiologic studies do not confirm an increased risk of cancer in exposed humans. Available evidence does not suggest that the agent is likely to cause cancer in humans except under uncommon or unlikely routes or levels of exposure.
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Molybdenum, as Mo; metal and insoluble compounds ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Molybdenum, as Mo; metal and insoluble compounds EPA (U.S. Environmental Protection Agency, 2011): Not Assessed under the IRIS program. ; Listed as: Molybdenum 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: Molybdenum and insoluble compounds (as Mo) NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed ; Listed as: Molybdenum (soluble compounds, as Mo) 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 CAS7439-98-7 (U.S. Environmental Protection Agency, 2011):
Oral: Slope Factor: RfD: 5x10(-3) mg/kg-day
Inhalation: Drinking Water:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS7439-98-7 (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. Adopted Value Adopted Value Adopted Value
- AIHA WEEL Values for CAS7439-98-7 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS7439-98-7 (National Institute for Occupational Safety and Health, 2007):
Listed as: Molybdenum and insoluble compounds (as Mo) REL: TWA: NIOSH REL*: STEL: Ceiling: Carcinogen Listing: (Not Listed) Not Listed Skin Designation: Not Listed Note(s): See Appendix D; [*Note: The REL and PEL also applies to other insoluble molybdenum compounds (as Mo).],
Listed as: Molybdenum (soluble compounds, as Mo) REL: IDLH: IDLH: 5000 mg Mo/m3 Note(s): Not Listed
IDLH: IDLH: 1000 mg Mo/m3 Note(s): Not Listed
- OSHA PEL Values for CAS7439-98-7 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
Listed as: Molybdenum (as Mo) (Soluble compounds) Table Z-1 for Molybdenum (as Mo) (Soluble compounds): 8-hour TWA: ppm: mg/m3: 5 Ceiling Value: Skin Designation: No Notation(s): Not Listed
Listed as: Molybdenum (as Mo) (Insoluble compounds) (Total dust) Table Z-1 for Molybdenum (as Mo) (Insoluble compounds) (Total dust): 8-hour TWA: ppm: mg/m3: 15 Ceiling Value: Skin Designation: No Notation(s): Not Listed
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS7439-98-7 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS7439-98-7 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS7439-98-7 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS7439-98-7 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS7439-98-7 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS7439-98-7 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS7439-98-7 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS7439-98-7 (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 CAS7439-98-7 (NFPA, 2002):
-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.
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 7439-98-7.
-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.
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS7439-98-7 (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 CAS7439-98-7 (NFPA, 2002):
EXPLOSION HAZARD
- Molybdenum is flammable or explosive in the form of dust and when exposed to heat or flame (Sax & Lewis, 1989).
DUST/VAPOR HAZARD
- Molybdenum is flammable or explosive in the form of dust and when exposed to heat or flame (Sax & Lewis, 1989).
- When heated to decomposition, molybdenum emits toxic fumes of Mo (Sax & Lewis, 1989).
REACTIVITY HAZARD
- Molybdenum is flammable or explosive in the form of dust and when exposed to heat or flame (Sax & Lewis, 1989).
- Molybdenum forms violent reactions with oxidants (eg, bromine trifluoride; bromine pentafluoride; chlorine trifluoride; potassium perchlorate; nitryl fluoride; fluorine; iodine pentafluoride; sodium peroxide; and lead dioxide) (Sax & Lewis, 1989).
- When heated to decomposition, molybdenum emits toxic fumes of Mo (Sax & Lewis, 1989).
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 CAS7439-98-7 (AIHA, 2006):
- DOE TEEL Values for CAS7439-98-7 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Molybdenum TEEL-0 (units = mg/m3): 15 TEEL-1 (units = mg/m3): 15 TEEL-2 (units = mg/m3): 15 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 CAS7439-98-7 (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, 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; 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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; 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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 CAS7439-98-7 (National Institute for Occupational Safety and Health, 2007):
IDLH: 5000 mg Mo/m3 Note(s): Not Listed IDLH: 1000 mg Mo/m3 Note(s): Not Listed
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.
"At the time of this review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices." (HSDB , 1992)
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Soil: Molybdenum is an important trace element. Its occurrence in the earth's crust is approximately 1 to 1.5 ppm. Its most important ores are molybdenite (MoS2) and wulfenite (PbMoO4) (Budavari, 1989).
- Soil: Alpine soils show greater sorption capacity than desert or agricultural soils; sorption is best in soils of low pH and high organic content (OHM/TADS , 1992).
- Other: Global mobilization of molybdenum is reported by weathering at 6 x 10(6) kg/molybdenum/year; by rivers at 19 x 10(6) kg/molybdenum/year; by mining at 76 x 10(6) kg/molybdenum/year; and by combustion (oil and coal) at 0.8 x 10(6) kg/molybdenum/year (HSDB , 1992).
ENVIRONMENTAL FATE AND KINETICS
OTHER Water: Persistency in water: Should precipitate out with natural calcium (OHM/TADS , 1992) Soil: Adding lime to soil increases molybdenum availability (HSDB , 1992).
ENVIRONMENTAL TOXICITY
Phytotoxic effects have been noted in sandy soil with as little as 10 ppm/month molybdenum (OHM/TADS , 1992). In general, soil levels should not exceed 50 ppm to avoid problems with certain livestock; other reports suggest a limit of 8 ppm molybdenum in the top 12 inches of soil (OHM/TADS , 1992).
- ECOTOXICITY VALUES (HSDB , 1992):
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Molybdenum is a dark-gray or black powder with metallic luster or a coherent mass of silver-white color; body-centered cubic structure (HSDB, 2005; Budavari, 1996).
PH
VAPOR PRESSURE
- 1 mmHg (at 3102 degrees C) (Sax & Lewis, 1989)
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
- TEMPERATURE AND/OR PRESSURE NOT LISTED
FREEZING/MELTING POINT
BOILING POINT
- Approximately 4825 degrees C (Budavari, 1996)
- 5560 degrees C (ACGIH, 1986)
SOLUBILITY
Molybdenum is practically insoluble in alkali hydroxides or fused alkalies (Budavari, 1996). Molybdenum is soluble in hot concentrated sulfuric or nitric acids and insoluble in hydrochloric acid and hydrogen fluoride, ammonia, sodium hydroxide, or dilute sulfuric acid (Sax & Lewis, 1987).
OTHER/PHYSICAL
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