10-Methylbenz[a]anthracene
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10-Methylbenz[a]anthracene
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CAS No:
2381-15-9
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Formula:
C19H14
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Chemical Name:
10-Methylbenz[a]anthracene
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Synonyms:
Benz[a]anthracene,10-methyl-;10-Methylbenz[a]anthracene;7-Methyl-1,2-benzanthracene;10-Monomethylbenz[a]anthracene;NSC 409456;10-Methylbenzo[a]anthracene;10-Methyltetraphene
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CAS No:
10-Methylbenz[a]anthracene Basic Attributes
242.314
242.31
SH803A2AAG
409456
DTXSID0073293
Yellow plates from alcohol
2902909090
Characteristics
0
6.37
1.2±0.1 g/cm3
183-183.6 °C
449.4±12.0 °C at 760 mmHg
217.8±13.7 °C
1.748
Soluble in ethanol, acetic acid
Precautions for safe handling: Avoid formation of dust and aerosols. Provide appropriate exhaust ventilation at places where dust is formed.
1.01X10-7 mm Hg at 25 deg C (est)
Henry's Law constant = 1.90X10-6 atm-cu m/mol at 25 °C (est)
Hydroxyl radical reaction rate constant = 1.31X10-10 cu cm/mole-sec at 25 °C (est)
Safety Information
Stable under recommended storage conditions.
P273, P391, P501
H400
SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.|SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.|Product: Offer surplus and non-recyclable solutions to a licensed disposal company; Contaminated packaging: Dispose of as unused product.
Incompatible materials: Strong oxidizing agents.
|Warning|H400 (100%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]|P273, P391, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H400: Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]
Eye/face protection: Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).|Skin protection: Handle with gloves.|Body Protection: Choose body protection in relation to its type, to the concentration and amount of dangerous substances, and to the specific work-place.|Respiratory protection: Respiratory protection is not required. Where protection from nuisance levels of dusts are desired, use type N95 (US) or type P1 (EN 143) dust masks. Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).|For more Personal Protective Equipment (PPE) (Complete) data for 10-Methylbenz(a)anthracene (6 total), please visit the HSDB record page.
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.|Advice for firefighters: Wear self contained breathing apparatus for fire fighting if necessary.
Keep container tightly closed in a dry and well-ventilated place.
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. 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.|Precautions for safe handling: Avoid formation of dust and aerosols. Provide appropriate exhaust ventilation at places where dust is formed.|Appropriate engineering controls: Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday.|Gloves must be inspected prior to use. Use proper glove removal technique (without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands.|For more Preventive Measures (Complete) data for 10-Methylbenz(a)anthracene (8 total), please visit the HSDB record page.
Permissible Exposure Limit: Table Z-1 8-hr Time Weighted Avg: 0.2 mg/cu m. /Coal tar pitch volatiles (benzene soluble fraction), anthracene, BaP, phenanthrene, acridine, chrysene, pyrene/
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/
Methylbenz(a)anthracenes, including 10-methylbenz(a)anthracene, were reported at a concentration range of 30-50 ng/mg extract in diesel engine exhaust of passenger cars(1). Methylbenz(a)anthracenes are found in airborne particulates from cigarette smoke condensate, stack gases, roofing tar extracts, and industrial effluents(2).
Toxicity
IDENTIFICATION AND USE: 10-Methylbenz(a)anthracene (10-MBA) is a solid. It could be formed from incomplete combustion of organic materials. It is used mostly in biochemical research. HUMAN EXPOSURE AND TOXICITY: There are no data available. ANIMAL STUDIES: Mice received dermal applications of 10-MBA, 300 ug/application, twice a week for 20 weeks. 72% of mice had dose-action related palillomas. There appeared to be little quantitative correspondence between carcinogenic and mutagenic potency for this group of chemicals.
10-Methylbenz(a)anthracene is one of many polycyclic aromatic hydrocarbons (PAH), a group of chemicals that are formed during the incomplete burning of coal, oil, gas, wood, garbage, or other organic substances. PAHs generally occur as complex mixtures, for example as part of combustion products such as soot, not as single compounds. PAHs occur naturally in volcanoes and forest fires. They can also be found in substances such as crude oil and coal. They are found throughout the environment in the air, water, and soil(1). /Polycyclic aromatic hydrocarbons/
Methylbenz(a)anthracenes are found in airborne particulates from cigarette smoke condensate, stack gases, roofing tar extracts and industrial effluents(1), which may result in 10-methylbenz(a)anthracene's release to the environment through various waste streams(SRC). There is no commercial production of this compound(2).
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 3.0X10+5(SRC), determined from a structure estimation method(2), indicates that 10-methylbenz(a)anthracene is expected to be immobile in soil(SRC). Volatilization of 10-methylbenz(a)anthracene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.9X10-6 atm-cu m/mole(SRC), using a fragment constant estimation method(3). However, adsorption to soil is expected to attenuate volatilization(SRC). 10-Methylbenz(a)anthracene is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.0X10-7 mm Hg at 25deg C(SRC), determined from a fragment constant method(2). 10-Methylbenz(a)anthracene was resistant to biodegradation using activated sludge in the Warburg test(4), suggesting that biodegradation is not expected to be an important fate process in soil(SRC).|AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 3.0X10+5(SRC), determined from a structure estimation method(2), indicates that 10-methylbenz(a)anthracene is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 1.9X10-6 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 30 and 220 days, respectively(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is about 860 years when adsorption is considered(5). According to a classification scheme(6), an estimated BCF of 4700(SRC), from an estimated log Kow of 6.07(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is very high, provided the compound is not metabolized by the organism(SRC). 10-Methylbenz(a)anthracene was resistant to biodegradation using activated sludge in the Warburg test(7), suggesting that biodegradation is not expected to be an important fate process in water(SRC).|ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 10-methylbenz(a)anthracene, which has an estimated vapor pressure of 1.0X10-7 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases. Vapor-phase 10-methylbenz(a)anthracene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 0.08 days(SRC), calculated from its rate constant of 1.3X10-10 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase 10-methylbenz(a)anthracene may be removed from the air by wet and dry deposition(SRC). 10-Methylbenz(a)anthracene absorbs UV light at wavelengths >290 nm(4) and, therefore, may be susceptible to direct photolysis by sunlight(SRC).
The rate constant for the vapor-phase reaction of 10-methylbenz(a)anthracene with photochemically-produced hydroxyl radicals has been estimated as 1.3X10-10 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 0.08 days at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). 10-Methylbenz(a)anthracene is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(2). 10-Methylbenz(a)anthracene absorbs UV light at wavelengths >290 nm(3) and, therefore, may be susceptible to direct photolysis by sunlight(SRC).
An estimated BCF of 4700 was calculated in fish for 10-methylbenz(a)anthracene(SRC), using an estimated log Kow of 6.07(1) and a regression-derived equation(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is very high, provided the compound is not metabolized by the organism(SRC). However, bioconcentration studies on compounds which are structurally similar suggest that bioconcentration may be lower than that indicated by the regression-derived equations due to the ability of some aquatic organisms to readily metabolize this polycyclic aromatic hydrocarbons of compounds(3).
Using a structure estimation method based on molecular connectivity indices(1), the Koc of 10-methylbenz(a)anthracene can be estimated to be 3.0X10+5(SRC). According to a classification scheme(2), this estimated Koc value suggests that 10-methylbenz(a)anthracene is expected to be immobile in soil(SRC).
The Henry's Law constant for 10-methylbenz(a)anthracene is estimated as 1.9X10-6 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 10-methylbenz(a)anthracene is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 30 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 220 days(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is about 860 years when adsorption is considered(3). 10-Methylbenz(a)anthracene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 10-Methylbenz(a)anthracene is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.0X10-7 mm Hg(SRC), determined from a fragment constant method(4).
Occupational exposure to 10-methylbenz(a)anthracene may occur through inhalation of dust particles contaminated with incomplete combustion products and dermal contact with incomplete combustion products containing 10-methylbenz(a)anthracene. The most likely pathway by which the general public is exposed to 10-methylbenz(a)anthracene is by inhalation due to the probable release of this substance from combustion fuels and cigarette smoke. (SRC)
Drug Information
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. /Aromatic hydrocarbons and related compounds/|Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary. ... For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 L of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . /Aromatic hydrocarbons and related compounds/|Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag-valve-mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Consider administering a beta agonist such as albuterol for severe bronchospasm ... . Monitor cardiac rhythm and treat arrhythmias if necessary ... . Start IV administration of D5W TKO /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam (Valium) or lorazepam (Ativan) ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Aromatics hydrocarbons and related compounds/
10-Methylbenz[a]anthracene Use and Manufacturing
10-Methylbenz[a]anthracene is a monomethylated polycyclic aromatic hydrocarbon with carcinogenic activity.
(1975) NOT PRODUCED COMMERCIALLY IN US|(1977) NOT PRODUCED COMMERCIALLY IN US
FORMED FROM INCOMPLETE COMBUSTION OF ORGANIC MATERIALS (EG, REFUSE BURNING, OPERATION OF MOTOR VEHICLES, INDUST PROCESSES)