CYCLOHEXENE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
CYCLOHEXENE BENZENETETRAHYDRIDE BENZENE, TETRAHYDRO- CYCLOHEX-1-ENE CYCLOHEXENE RING CYKLOHEKSEN (Polish) HEXANAPHTHYLENE TETRAHYDROBENZENE 1,2,3,4-TETRAHYDROBENZENE 3,4,5,6-TETRAHYDROBENZENE
IDENTIFIERS
SYNONYM REFERENCE
- ((HSDB, 1995); RTECS , 1995)AAR, 1992
USES/FORMS/SOURCES
Cyclohexene is used as an alkylation component and in the organic synthesis of adipic acid, maleic acid, hexahydrobenzoic acid, aldehydes, and butadiene (Budavari, 1989). It is also used as a catalyst solvent (ACGIH, 1991). Other uses of cyclohexene include oil and wax extraction, and stabilization of high-octane gasoline (ACGIH, 1991; Clayton & Clayton, 1994; ITI, 1988).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Cyclohexene is a mild to moderate respiratory irritant and CNS depressant; it may also be moderately toxic by ingestion. With direct contact, the liquid defats the skin. Systemic toxic effects of acute or chronic exposure have not been reported in humans.
- In an experimental study, a significant increase in serum alkaline phosphatase and decrease in body weight gain were noted; however, most of the parameters in the hematologic and biochemical profiles were within normal limits.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (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 130 (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 - Promptly wash the contaminated skin with soap and water. If this chemical penetrates the clothing, promptly remove the clothing and wash the skin with soap and water. Get medical attention promptly. INHALATION EXPOSURE - Move the exposed person to fresh air at once. If breathing has stopped, perform artificial respiration mouth-to-mouth resuscitation. 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, respiratory system, and CNS (National Institute for Occupational Safety and Health, 2007).
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.
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 In general, gastric emptying is not indicated unless the patient has a history of large ingestions or ingestion of hydrocarbons which may produce renal, liver, or central nervous system (CNS) toxicity (ie, halogenated hydrocarbons or petroleum distillates with additives). Gastric emptying is not indicated following accidental ingestion of small amounts of gasoline, kerosene, mineral seal oil, furniture polish, mineral oil, or motor oils. 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.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
MAXIMUM TOLERATED EXPOSURE
A chronic inhalation study was conducted with rats, guinea pigs, and rabbits at 150, 300, or 600 ppm of cyclohexene 6 hours/day, 5 days/week for 6 months. Although a significant increase in serum alkaline phosphatase occurred in all three groups and rats showed a decrease in body weight gain at the 600 ppm concentration, most of the parameters in the hematologic profile and the biochemical profile were within normal limits (ACGIH, 1991). Mice lost their righting reflex with exposure to approximately 9000 ppm of cyclohexene (Hathaway et al, 1991). Dogs inhaling cyclohexene vapor (concentration not stated) exhibited symptoms characterized by muscular quivering and incoordination (Hathaway et al, 1991).
- Carcinogenicity Ratings for CAS110-83-8 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed ; Listed as: Cyclohexene 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: Cyclohexene 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 CAS110-83-8 (U.S. Environmental Protection Agency, 2011):
References: ITI, 1988 LCLo- (INHALATION)MOUSE: LD50- (ORAL)MOUSE:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS110-83-8 (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 CAS110-83-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS110-83-8 (National Institute for Occupational Safety and Health, 2007):
Listed as: Cyclohexene REL: TWA: 300 ppm (1015 mg/m(3)) STEL: Ceiling: Carcinogen Listing: (Not Listed) Not Listed Skin Designation: Not Listed Note(s):
IDLH: IDLH: 2000 ppm Note(s): Not Listed
- OSHA PEL Values for CAS110-83-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS110-83-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS110-83-8 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS110-83-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS110-83-8 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS110-83-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS110-83-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS110-83-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS110-83-8 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2256 (49 CFR 172.101, 2005):
- ICAO International Shipping Name for UN2256 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS110-83-8 (NFPA, 2002):
Listed as: Cyclohexene Hazard Ratings: Health Rating (Blue): 1 Flammability Rating (Red): 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
Instability Rating (Yellow): 0 Oxidizer/Water-Reactive Designation: Not Listed
-HANDLING AND STORAGE
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (ERG, 2004)
- Avoid breathing vapors. Keep upwind. Wear positive pressure self-contained breathing apparatus. Wear appropriate chemical protective gloves, boots and goggles. Do not handle broken packages unless wearing appropriate personal protective equipment. If contact with the material is anticipated, wear appropriate chemical protective clothing (AAR, 1992).
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 110-83-8.
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (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.
Cyclohexene is a very dangerous fire hazard when exposed to flame. It can react with oxidizers (Lewis, 1992).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS110-83-8 (NFPA, 2002):
Listed as: Cyclohexene Flammability Rating: 3 (3) Flammable. Liquids and solids that can be ignited under almost all ambient temperature conditions. Including liquids with a flash point below 73 degrees F and a boiling point above 100 degrees F, solid materials which form coarse dusts that burn rapidly without becoming explosive, materials which burn rapidly by reason of self-contained oxygen (ie, organic peroxides), and materials which ignite spontaneously when exposed to air.
- INITIATING OR CONTRIBUTING PROPERTIES
- FIRE CONTROL/EXTINGUISHING AGENTS
- FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (ERG, 2004)
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (ERG, 2004)
Water spray, fog or regular 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 130 (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 CAS110-83-8 (NFPA, 2002):
- To fight fire, use foam, carbon dioxide, or dry chemical (Lewis, 1992) AAR, 1992).
- Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Keep runoff water out of sewers and water sources (AAR, 1992).
- If fire involving cyclohexene becomes uncontrollable or container is exposed to direct flame, consider evacuation of one-half mile radius (AAR, 1992).
EXPLOSION HAZARD
- Cyclohexene forms explosive peroxides with oxygen upon storage (NIOSH, 1995).
REACTIVITY HAZARD
- Cyclohexene forms explosive peroxides with oxygen upon storage (NIOSH, 1995).
- Cyclohexene is a very dangerous fire hazard when exposed to flame. It can react with oxidizers (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 130 (ERG, 2004)
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (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 130 (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.
- If fire involving cyclohexene becomes uncontrollable or container is exposed to direct flame, consider evacuation of one-half mile radius (AAR, 1992).
- If material is leaking, but not on fire, consider evacuation from downwind area based on amount of material spilled, location, and weather conditions (AAR, 1992).
- AIHA ERPG Values for CAS110-83-8 (AIHA, 2006):
- DOE TEEL Values for CAS110-83-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Cyclohexene TEEL-0 (units = ppm): 300 TEEL-1 (units = ppm): 300 TEEL-2 (units = ppm): 500 TEEL-3 (units = ppm): 2000 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 CAS110-83-8 (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 CAS110-83-8 (National Institute for Occupational Safety and Health, 2007):
IDLH: 2000 ppm Note(s): Not Listed
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (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 130 (ERG, 2004)
LARGE SPILL PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 130 (ERG, 2004) Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Attempt to stop leak if it can be done without undue personnel hazard. Use water spray to knock-down vapors (AAR, 1992).
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- Cyclohexene may be released to the environment as a fugitive emission during its production and use and in motor vehicle exhaust ((HSDB, 1995)).
ENVIRONMENTAL FATE AND KINETICS
If released to the atmosphere, cyclohexene is expected to undergo a rapid, aerosol-forming reaction with ozone ((HSDB, 1995)). An experimental rate constant for this reaction of 2.04 x 10(-16) cm(3)/molec-sec at 21 degrees C translates to an atmospheric half-life of 1.9 hours, using an average atmospheric ozone concentration of 7 x 10(+11) molec/cm(3). Aerosol formation in this reaction, (ie, organic acid formation), was found to increase with increasing humidity ((HSDB, 1995)).
Cyclohexene is also expected to undergo a relatively rapid vapor-phase oxidation with photochemically produced hydroxyl radicals, with an estimated half-life of 8.3 hours, based on an experimental rate constant of 6.7 x 10(-11) cm(3)/molec-sec at 25 degrees C ((HSDB, 1995)). An experimental rate constant for the gas-phase reaction of cyclohexene with nitrate radicals at night of 1.9 x 10(-12) cm(3)/molec-sec at 25 degrees C translates to a half-life of 3.7 hours, using an average nitrate radical concentration of 2 x 10(+8) molec/cm(3) ((HSDB, 1995)). Cyclohexene's water solubility (213 mg/L) indicates that it may undergo atmospheric removal by wet deposition processes ((HSDB, 1995)).
SURFACE WATER If released to water, cyclohexene may biodegrade under aerobic conditions ((HSDB, 1995)). Based upon the water solubility (213 mg/L at 25 degrees C) and octanol/water partition coefficient (2.86), the bioconcentration factor for cyclohexene can be estimated to range from 30 to 87 using regression-derived equations, indicating that bioconcentration in fish and aquatic organisms will not be a significant process ((HSDB, 1995)). Cyclohexene's Henry's Law constant, 4.55 x 10(-2) atm-m(3)/mole at 25 degrees C, indicates that volatilization to the atmosphere will be rapid ((HSDB, 1995)). Estimated soil adsorption coefficients ranging from 228 to 856 indicate that adsorption to sediment and suspended organic matter will not be a significant fate process ((HSDB, 1995)).
TERRESTRIAL If released to soil, cyclohexene is expected to biodegrade in aerobic soils ((HSDB, 1995)). Based upon the water solubility (213 mg/L at 25 degrees C) and octanol/water partition coefficient (2.86), the soil adsorption coefficient for cyclohexene can be estimated to range from 228 to 856 using regression-derived equations, indicating that cyclohexene will display low to moderate mobility in soil ((HSDB, 1995)). Cyclohexene's Henry's Law constant, 4.55 x 10(-2) atm-m(3)/mole at 25 degrees C, and vapor pressure, 89 mmHg at 25 degrees C, indicate that cyclohexene will rapidly volatilize from both moist and dry soils ((HSDB, 1995)).
OTHER AIR Cyclohexene is expected to undergo a rapid, aerosol-forming reaction with ozone, with an atmospheric half-life of 1.9 hours ((HSDB, 1995)). Cyclohexene is also expected to undergo a relatively rapid vapor-phase oxidation with photochemically produced hydroxyl radicals, with an estimated half-life of 8.3 hours ((HSDB, 1995)). The estimated half-life for the gas-phase reaction of cyclohexene with nitrate radicals at night is 3.7 hours ((HSDB, 1995)).
WATER
BIODEGRADATION
- Cyclohexene is expected to biodegrade under aerobic conditions in water and soil ((HSDB, 1995)).
BIOACCUMULATION
Based upon the water solubility of cyclohexene (213 mg/L at 25 degrees C) and octanol/water partition coefficient (2.86), the bioconcentration factor for cyclohexene can be estimated to range from 30 to 87 using regression-derived equations. The magnitude of these values indicates that bioconcentration in fish and aquatic organisms will not be a significant process ((HSDB, 1995)).
ENVIRONMENTAL TOXICITY
- No information found at the time of this review.
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Cyclohexene is a colorless liquid (Lewis, 1992).
VAPOR PRESSURE
- 160 mmHg (at 38 degrees C) (Lewis, 1992)
- 89 mmHg (at 25 degrees C) ((HSDB, 1995))
- 67 mmHg (at 20 degrees C) (ACGIH, 1991)
SPECIFIC GRAVITY
- OTHER TEMPERATURE AND/OR PRESSURE
0.8102 (at 20/4 degrees C) (Lewis, 1992) 0.8098 (at 20/4 degrees C) (Budavari, 1989)
FREEZING/MELTING POINT
BOILING POINT
- 83 degrees C (Lewis, 1992)
FLASH POINT
- <-6 degrees C; <21.2 degrees F (Lewis, 1992; ACGIH, 1991)
AUTOIGNITION TEMPERATURE
- 590 degrees F (Lewis, 1992)
- 471 degrees F (NFPA, 1991)
EXPLOSIVE LIMITS
SOLUBILITY
It is soluble in alcohol (Lewis, 1992). It is also soluble in ether, acetone, benzene, carbon tetrachloride, and petroleum ether ((HSDB, 1995)).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = 2.86 ((HSDB, 1995))
HENRY'S CONSTANT
- 4.55 x 10(-2) atm-m(3)/mol (at 25 degrees C) ((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.
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