METHYL ISOBUTYL CARBINOL
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
METHYL ISOBUTYL CARBINOL ALCOOL METHYL AMYLIQUE (French) 1,3-DIMETHYLBUTANOL ISOBUTYLMETHYLCARBINOL ISOBUTYLMETHYLMETHANOL MAOH METHYL AMYL ALCOHOL METHYLISOBUTYL CARBINOL METHYL-ISOBUTYLKARBINOL (Czech) 2-METHYL-4-PENTANOL 4-METHYLPENTANOL-2 4-METHYL-2-PENTANOL METILAMIL ALCOHOL (Italian) 4-METILPENTAN-2-OLO (Italian) MIBC MIC 3-MIC 2-PENTANOL, 4-METHYL 4-PENTANOL, 2-METHYL-
IDENTIFIERS
SYNONYM REFERENCE
- (HSDB , 1995; RTECS , 1995)
USES/FORMS/SOURCES
Methyl isobutyl carbinol is used as a solvent for dyestuffs, oils, gums, waxes, resins, nitrocellulose, and ethylcellulose (Lewis, 1993). It is used in organic synthesis, froth flotation, and in brake fluids (Lewis, 1993). In addition, it is used in the manufacture of lubricant additives, solvents, lacquers, and plasticizers (HSDB , 1995).
Methyl isobutyl carbinol is derived from methyl isobutyl ketone (Lewis, 1993). Methyl isobutyl carbinol may be formed naturally, as it was detected in a mixture of volatiles from mountain Beaufort cheese (HSDB , 1995).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Methyl isobutyl carbinol is irritating to the eyes, skin, and mucous membranes. It is moderately toxic by ingestion, dermal exposure, and intraperitoneal exposure; it is mildly toxic by inhalation.
- Exposure to high concentrations causes narcosis in experimental animals and it is expected that severe exposure in humans would produce the same effect. Exposure to the vapors may cause headache, dizziness, or suffocation.
- In experimental animals, chloroform-induced hepatotoxicity was potentiated by methyl isobutyl carbinol; this effect was attributed to methyl isobutyl ketone, the metabolite, and not the alcohol.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. Wash skin with soap and water. Keep victim warm and quiet. In case of burns, immediately cool affected skin for as long as possible with cold water. Do not remove clothing if adhering to skin. 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 - Flush the contaminated skin with water promptly. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water promptly. If irritation persists after washing, get medical attention. INHALATION EXPOSURE - Move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration. Keep the affected person warm and at rest. Get medical attention as soon as possible. INGESTION EXPOSURE - If this chemical has been swallowed, get medical attention immediately. TARGET ORGANS - Eyes, skin, and central nervous system (National Institute for Occupational Safety and Health, 2007).
GENERAL - Move victims of inhalation exposure from the toxic environment and administer 100% humidified supplemental oxygen with assisted ventilation as required. Exposed skin and eyes should be copiously flushed with water. Because of the potential for rapid onset of CNS depression or seizures with possible aspiration of gastric contents, EMESIS SHOULD NOT BE INDUCED. Cautious gastric lavage followed by administration of activated charcoal may be of benefit if the patient is seen soon after the exposure.
INHALATION EXPOSURE - INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm.
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.
INGESTION EXPOSURE - Because of the potential for gastrointestinal tract irritation or CNS depression, do not induce emesis. Significant esophageal or gastrointestinal tract irritation or burns may occur following ingestion. The possible benefit of early removal of some ingested material by cautious gastric lavage must be weighed against potential complications of bleeding or perforation. GASTRIC LAVAGE: Consider after ingestion of a potentially life-threatening amount of poison if it can be performed soon after ingestion (generally within 1 hour). Protect airway by placement in the head down left lateral decubitus position or by endotracheal intubation. Control any seizures first. ACTIVATED CHARCOAL: Administer charcoal as a slurry (240 mL water/30 g charcoal). Usual dose: 25 to 100 g in adults/adolescents, 25 to 50 g in children (1 to 12 years), and 1 g/kg in infants less than 1 year old. Observe patients with ingestion carefully for the possible development of esophageal or gastrointestinal tract irritation or burns. If signs or symptoms of esophageal irritation or burns are present, consider endoscopy to determine the extent of injury.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
After exposure to 2000 ppm of methyl isobutyl carbinol for 8 hours, 5 out of 6 rats died (Hathaway, 1991). Groups of 10 mice were exposed to 20 mg/L (4600 ppm) of methyl isobutyl carbinol for 1, 4, 8.5, 10, and 15 hours. Six mice from one group died after 10 hours of exposure and eight from another group died after 15 hours (ACGIH, 1991).
MAXIMUM TOLERATED EXPOSURE
Acute, chronic, and systemic effects have not been reported in humans (Hathaway, 1991). Exposure for 15 minutes to 50 ppm of methyl isobutyl carbinol vapor caused throat and nose irritation (Clayton & Clayton, 1994).
Seven out of 10 mice exposed to 4600 ppm for 4 hours experienced anesthetization. Ten out of 10 in another group also experienced anesthetization after 8.5 hours (ACGIH, 1991). At high concentrations, methyl isobutyl carbinol causes narcosis in animals (Hathaway, 1991).
- Carcinogenicity Ratings for CAS108-11-2 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Methyl isobutyl carbinol 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: Methyl isobutyl carbinol 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 CAS108-11-2 (U.S. Environmental Protection Agency, 2011):
References: Clayton & Clayton, 1994 Lewis, 1992 RTECS, 1995 Note: All values are from RTECS, 1995, unless otherwise noted.
CALCULATIONS
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS108-11-2 (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 CAS108-11-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS108-11-2 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS108-11-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS108-11-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS108-11-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS108-11-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS108-11-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS108-11-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS108-11-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS108-11-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS108-11-2 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2053 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN2053 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS108-11-2 (NFPA, 2002):
-HANDLING AND STORAGE
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- Wear appropriate chemical protective boots, gloves, and goggles (AAR, 1994).
- Workers should wash skin as soon as it becomes contaminated (NIOSH, 1995).
- Wet or significantly contaminated clothing should be removed and replaced. Workers need not change clothing at the end of the shift unless clothing is contaminated (NIOSH, 1995).
- Do not wear contact lenses when working with this material (HSDB , 1995).
- Stay upwind and avoid breathing vapors (AAR, 1994).
EYE/FACE PROTECTION
- Wear goggles or face shield (CHRIS , 1995).
- If chemical contacts eyes, flush with copious amounts of water while holding eyelids open (CHRIS , 1995).
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 108-11-2.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004) HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Methyl isobutyl carbinol is flammable when exposed to heat or flame (Lewis, 1992).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS108-11-2 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Dry chemical, CO2, water spray or alcohol-resistant foam. Do not use dry chemical extinguishers to control fires involving nitromethane or nitroethane.
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Water spray, fog or alcohol-resistant foam. Do not use straight streams. Move containers from fire area if you can do it without risk.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. 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 CAS108-11-2 (NFPA, 2002):
EXPLOSION HAZARD
- When exposed to heat or flame, methyl isobutyl carbinol is a moderate explosion hazard (Lewis, 1992).
DUST/VAPOR HAZARD
- Anesthesia can result from inhalation of high concentrations (Lewis, 1992).
- Vapors will cause moderate, temporary irritation to workers (CHRIS , 1995).
REACTIVITY HAZARD
- Methyl isobutyl carbinol can react with oxidizing materials (Lewis, 1992).
EVACUATION PROCEDURES
- Editor's Note: This material is not listed in the Table of Initial Isolation and Protective Action Distances.
- LARGE SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (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 129 (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 for at least 50 meters (150 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate closed spaces before entering.
- AIHA ERPG Values for CAS108-11-2 (AIHA, 2006):
- DOE TEEL Values for CAS108-11-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS108-11-2 (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 CAS108-11-2 (National Institute for Occupational Safety and Health, 2007):
IDLH: 400 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor suppressing foam may be used to reduce vapors. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. Use clean non-sparking tools to collect absorbed material.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 129 (ERG, 2004)
In screening tests using activated sludge in a medium consisting of approximately 16,000 ppm ethyl alcohol and 100 ppm urea, the rate constant of disappearance of methyl isobutyl carbinol was 0.432/hr. This corresponds to a half-life of 17 hours (HSDB, 2004). 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.
Sorbent foams can be applied to a slick and oil skimming equipment can be used. Carbon or peat should be applied to the dissolved portion (OHM/TADS , 1995). Methyl isobutyl carbinol may be sprayed into an incinerator or burned in paper packaging. If necessary, additional flammable solvent may be added (OHM/TADS , 1995).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- The compound may be released to the environment from industrial sources that use it in manufacturing processes (HSDB, 2004).
ENVIRONMENTAL FATE AND KINETICS
When released to the atmosphere, it is expected that methyl isobutyl carbinol will exist mainly in the vapor phase. This assumption is based on an experimental vapor pressure of 5.3 mmHg at 25 degrees C (HSDB, 2004). A rate constant of 7.1 x 10(-12) cm(3)/molecule-sec at 25 degrees C was measured for the vapor-phase reaction of methyl isobutyl carbinol with photochemically produced hydroxyl radicals. This rate constant corresponds to an atmospheric half-life of 2.3 days at an atmospheric concentration of 5 x 10(5) hydroxyl radicals per cm(3) (HSDB, 2004).
SURFACE WATER If released to water, methyl isobutyl carbinol is not expected to adsorb to sediment and suspended particulates or to bioconcentrate in aquatic organisms. This expectation is based on the organic carbon partition coefficient (Koc) and bioconcentration factor, estimated from log octanol-water partition coefficient (log Kow) and water solubility, respectively (HSDB, 2004). Methyl isobutyl carbinol is not expected to directly photolyze or hydrolyze (HSDB, 2004). Based on volatilization experiments in a model river and model pond, it is probable that methyl isobutyl carbinol will volatilize from surface waters (HSDB, 2004). The volatilization half-life for methyl isobutyl carbinol in a 1 meter deep river flowing 1 m/sec with a wind velocity of 3 m/sec was estimated to be 23 hr at 25 degrees C, based upon an experimental Henry's Law constant of 4.45 x 10(-5) atm-m(3)/mole (HSDB, 2004). From a model pond, which considers the adsorption effect, the volatilization half-life was estimated to be 10.6 days (HSDB, 2004).
GROUND WATER
TERRESTRIAL The mobility of methyl isobutyl carbinol in soil is very high based on an estimated Koc values of 143 and 21, estimated from log Kow and water solubility values, respectively. Thus, it can leach through soil (HSDB, 2004). It will not hydrolyze in moist soil, but if it is near the soil surface, it may volatilize based on estimated volatilization rates from water (HSDB, 2004).
ABIOTIC DEGRADATION
- Methyl isobutyl carbinol exists mainly in the vapor phase in air. In water, it is not expected to adsorb to sediment and suspended particulates or to bioconcentrate in aquatic organisms. In surface water, methyl isobutyl carbinol will more likely volatilize versus directly photolyze or hydrolyze. Its mobility in soil is very high. While it's unlikely to hydrolyze in moist soil, if it is near the soil's surface, it will more likely volatilize. Laboratory studies show methyl isobutyl carbinol will likely biodegrade in soil (HSDB, 2004).
BIODEGRADATION
- Methyl isobutyl carbinol may biodegrade in soil. This assumption is based on laboratory studies that revealed rapid biodegradation in aqueous screening tests using sewage and activated sludge inoculum (HSDB, 2004).
BIOACCUMULATION
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Methyl isobutyl carbinol is a clear, stable, oily liquid with a mild alcohol odor (Lewis, 1992; CHRIS , 1995).
VAPOR PRESSURE
- 2.8 mmHg (at 20 degrees C) (Lewis, 1992)
- 3.52 mmHg (at 20 degrees C) (ACGIH, 1991)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
DENSITY
- OTHER TEMPERATURE AND/OR PRESSURE
FREEZING/MELTING POINT
BOILING POINT
- 131.8 degrees C (ACGIH, 1991)
FLASH POINT
- 41.11 degrees C (closed cup) (ACGIH, 1991)
EXPLOSIVE LIMITS
SOLUBILITY
2% (percentage by weight) (NIOSH, 1995) Methyl isobutyl carbinol is slightly soluble in water (ACGIH, 1991).
Methyl isobutyl carbinol is miscible with most organic solvents (ACGIH, 1991). It is soluble in alcohol and ether (HSDB , 1995).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = 1.43 (HSDB , 1995)
SPECTRAL CONSTANTS
OTHER/PHYSICAL
-REFERENCES
GENERAL BIBLIOGRAPHY- 40 CFR 372.28: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Lower thresholds for chemicals of special concern. National Archives and Records Administration (NARA) and the Government Printing Office (GPO). Washington, DC. Final rules current as of Apr 3, 2006.
- 40 CFR 372.65: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Chemicals and Chemical Categories to which this part applies. National Archives and Records Association (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Apr 3, 2006.
- 49 CFR 172.101 - App. B: Department of Transportation - Table of Hazardous Materials, Appendix B: List of Marine Pollutants. National Archives and Records Administration (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Aug 29, 2005.
- 49 CFR 172.101: Department of Transportation - Table of Hazardous Materials. National Archives and Records Administration (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Aug 11, 2005.
- 62 FR 58840: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 1997.
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- 65 FR 39264: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
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