Not classified.
none
none
none
none
none
no data available
Fresh air, rest.
Remove contaminated clothes. Rinse and then wash skin with water and soap.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth.
SYMPTOMS: Symptoms of exposure to this compound may include irritation of the skin, eyes, mucous membranes and upper respiratory tract. If ingested, it can cause vomiting. Chronic exposure may result in kidney and liver damage. ACUTE/CHRONIC HAZARDS: This compound is harmful by inhalation, ingestion or skin absorption. It is an irritant of the skin, eyes, mucous membranes and upper respiratory tract. When heated to decomposition it emits toxic fumes of carbon monoxide and carbon dioxide. (NTP, 1992)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Naphthalene and Related Compounds
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical, or carbon dioxide.
Flash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
Use water spray, dry powder, foam, carbon dioxide.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Methods and materials for containment and cleaning up: Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed containers for disposal.
NO open flames. Closed system, dust explosion-proof electrical equipment and lighting. Prevent deposition of dust. Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Separated from strong oxidants. Provision to contain effluent from fire extinguishing. Store in an area without drain or sewer access.Keep container tightly closed in a dry and well-ventilated place. Storage class (TRGS 510): Non Combustible Solids.
Component | Acenaphthene |
---|---|
CAS No. | 83-32-9 |
Recommended Exposure Limit: 10 Hr Time-Weighted Avg: 0.1 mg/cu m (cyclohexane-extractable fraction). /Coal tar pitch volatiles/ NIOSH considers coal tar pitch volatiles to be potential occupational carcinogens. NIOSH usually recommends that occupational exposures to carcinogens be limited to the lowest feasible concentration. /Coal tar pitch volatiles/ |
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear safety goggles.
Protective gloves.
Use local exhaust or breathing protection.
no data available
Acenaphthene is a white needles. Melting point 93.6°C. Soluble in hot alcohol. Denser than water and insoluble in water. Hence sinks in water. May irritate skin and mucous membranes. Emits acrid smoke and irritating fumes when heated to decomposition. Derived from coal tar and used to make dyes, pharmaceuticals, insecticides, fungicides, and plastics.
White needles
no data available
122°C(lit.)
241°C(lit.)
Combustible.
no data available
38°C(lit.)
>450 °C
no data available
no data available
no data available
less than 1 mg/mL at 68° F (NTP, 1992)
log Kow = 3.92
10 mm Hg ( 131 °C)
1.069
5.32 (vs air)
no data available
NIOSH considers coal tar pitch volatiles to be potential occupational carcinogens. Coal tar pitch volatiles
On combustion, forms toxic gases including carbon monoxide. Reacts with strong oxidants.
Stable under recommended storage conditions.
This chemical is a combustible solid.Dust explosion possible if in powder or granular form, mixed with air.ACENAPHTHENE is incompatible with strong oxidizing agents. Incompatible with ozone and chlorinating agents. Forms crystalline complexes with desoxycholic acid (NTP, 1992).
no data available
Incompatible materials: Strong oxidizing agents.
Hazardous decomposition products formed under fire conditions - Carbon oxides.
no data available
no data available
no data available
no data available
no data available
no data available
no data available
See Notes.
A harmful concentration of airborne particles can be reached quickly when dispersed.
AEROBIC: Acclimated mixed cultures in mineral salt media were able to degrade 50% of a crude oil containing acenaphthene within 48 hr(1). Grab samples of groundwater aquifer soil that had acclimated to creosote wastes containing acenaphthene were able to degrade acenaphthene at concentration between 0.02 and 0.12 ppm under aerobic conditions at 25 deg C for a 56 day period at an average rate of 130% per week(2); an average loss of 5.0% per week was observed for autoclaved controls(2). Unacclimated material from the same aquifer degraded acenaphthene at an average rate of 6.6% per week; however, autoclaved controls lost acenaphthene at an overall rate of 9.2% per week(2). The biotransformation half-life for 2 mg/L of acenaphthene in hard water with zero suspended solids was 24.8 days(3). The half-lives for 2 mg/L of acenaphthene in hard water with suspended solid concentration of 52, 403 and 601 mg/L from Roselawn Pond, Denton, TX were 3.52, 4.03 and 2.23 days, respectively(3). The half-lives for 2 mg/L of acenaphthene in hard water with suspended solid concentrations of 83, 397 and 591 mg/L from Pat Mayseake, Paris, TX were 4.91, 1.20 and 0.83 days, respectively(3); all half-lives were corrected for abiotic losses by controls(3). Acenaphthene, present at 100 mg/L, reached 0% of its theoretical BOD in 4 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(4).
After a 28 day exposure to an average water concentration of 8.94 ug/L, the log BCF of acenaphthene in the tissue of bluegill sunfish (Lepomis macrochirus) was 2.59 (BCF of 389(1,2). A BCF range of 254-1270 was measured in fish for acenaphthene(SRC), using carp (Cyprinus carpio) which were exposed over an 8-week period to 0.003-0.03 mg/L(3). According to a classification scheme(4), the BCF range suggests the potential for bioconcentration in aquatic organisms is high to very high(SRC), provided the compound is not metabolized by the organism(SRC). PAHs may not bioconcentrate in aquatic organisms which contain microsomal oxidase, such as fish, as this enzyme enables the rapid metabolism of certain polycyclic aromatic hydrocarbons(4). Some marine organisms have no detectable aryl hydrocarbons hydroxylase enzyme systems, namely: phytoplankton, certain zooplankton, mussels (Mytilus edulis), scallops (Placopecten sp), and snails (Litternia littorea)(5). Those organisms which lack a metabolic detoxification enzyme system, tend to accumulate polycyclic aromatic hydrocarbons(5).
Acenaphthene has a reported experimental log Koc value of 3.59 (Koc of 3890) in soil(1). Desorption-sorption tests using 11 soils found a log Koc range of 3.40-5.33 (Koc of 2510-2.14X10+5)(2). The log Koc of acenaphthene in 16 historically contaminated sediments ranged from 2.97 to 5.87 (Koc of 933 to 7.4X10+5 with a median of 4.39 (Koc of 2.45X10+4)(3). According to a classification scheme(4), the Koc range in soil suggests that acenaphthene is expected to have slight to no mobility in soil.
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: UN3077 (For reference only, please check.)
IMDG: UN3077 (For reference only, please check.)
IATA: UN3077 (For reference only, please check.)
ADR/RID: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
IMDG: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
IATA: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
ADR/RID: 9 (For reference only, please check.)
IMDG: 9 (For reference only, please check.)
IATA: 9 (For reference only, please check.)
ADR/RID: III (For reference only, please check.)
IMDG: III (For reference only, please check.)
IATA: III (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Acenaphthene occurs as a pure substance and also as a component of polyaromatic hydrocarbon (PAH) mixtures.Human population studies have associated PAH's exposure with cancer and cardiovascular diseases.Insufficient data are available on the effect of this substance on human health, therefore utmost care must be taken.