1-METHYLPHENANTHRENE
1-METHYLPHENANTHRENE Basic information
- Product Name:
- 1-METHYLPHENANTHRENE
- Synonyms:
-
- 1-METHYLPHENANTHRENE
- 1-methyl-phenanthren
- PHENANTHRENE,1-METHYL-
- 1-Methylphenanthrene 100mg [832-69-9]
- NSC 146583
- 1-MethylphenanthreneSolution,2,000mg/L,1ml
- 1-Methylphenanthrene @50 μg/mL in Toluene
- 1-MethylphenanthreneSolution,5,000mg/L,1ml
- CAS:
- 832-69-9
- MF:
- C15H12
- MW:
- 192.26
- EINECS:
- 212-622-1
- Mol File:
- 832-69-9.mol
1-METHYLPHENANTHRENE Chemical Properties
- Melting point:
- 123°C
- Boiling point:
- 353.25°C (rough estimate)
- Density
- 1.0561 (estimate)
- refractive index
- 1.6031 (estimate)
- storage temp.
- Room Temperature
- solubility
- Soluble in alcohol (Weast, 1986)
- form
- Solid
- color
- White powder or solid.
- Water Solubility
- 269ug/L(25 ºC)
- Henry's Law Constant
- 1.56, 2.33, 3.42, 4.93, and 6.68 x 10-5 atm?m3/mol at 4.1, 11.0, 18.0, 25.0, and 31.0 °C, respectively (Bamford et al., 1998)
- IARC
- 3 (Vol. Sup 7, 92) 2010
- EPA Substance Registry System
- 1-Methylphenanthrene (832-69-9)
1-METHYLPHENANTHRENE Usage And Synthesis
Uses
1-Methylphenanthrene is a polycyclic aromatic hydrocarbon that has been found in particulate matter from small-scale biomass combustion from old and modern technologies and that has caused acute systemic and lung inflammation in mice after intratracheal aspiration.
Definition
ChEBI: A member of the class of phenanthrenes that is phenanthrene substituted by a methyl group at position 1.
Synthesis Reference(s)
The Journal of Organic Chemistry, 45, p. 2009, 1980 DOI: 10.1021/jo01298a054
Tetrahedron Letters, 6, p. 359, 1965
General Description
White crystalline powder.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as 1-METHYLPHENANTHRENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction. 1-METHYLPHENANTHRENE is sensitive to excessive heat and light.
Fire Hazard
Flash point data for 1-METHYLPHENANTHRENE are not available. 1-METHYLPHENANTHRENE is probably combustible.
Source
Detected in 8 diesel fuels at concentrations ranging from 0.10 to 210 mg/L with a mean
value of 44.33 mg/L (Westerholm and Li, 1994). Identified in a South Louisiana crude oil at a
concentration of 111 ppm (Pancirov and Brown, 1975). Schauer et al. (1999) reported 1-
methylphenanthrene in diesel fuel at a concentration of 28 μg/g and in a diesel-powered mediumduty
truck exhaust at an emission rate of 17.0 μg/km.
California Phase II reformulated gasoline contained 1-methylphenathrene at a concentration of
3.91 g/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without
catalytic converters were approximately 1.63 and 122 μg/km, respectively (Schauer et al., 2002).
Schauer et al. (2001) measured organic compound emission rates for volatile organic
compounds, gas-phase semi-volatile organic compounds, and particle-phase organic compounds
from the residential (fireplace) combustion of pine, oak, and eucalyptus. The respective gas-phase
and particle-phase emission rates of 1-methylphenanthrene were 2.22 and 0.579 mg/kg of pine
burned and 1.04 and 0.050 mg/kg of oak burned. The gas-phase emission rate was 0.720 mg/kg of
eucalyptus burned.
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