Basic information Safety Supplier Related

1-METHYLPHENANTHRENE

Basic information Safety Supplier Related

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
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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)
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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.

1-METHYLPHENANTHRENESupplier

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