Product Name

  • Name

    2-METHYLPHENANTHRENE

  • EINECS 219-791-0
  • CAS No. 2531-84-2
  • Article Data46
  • CAS DataBase
  • Density 1.105 g/cm3
  • Solubility
  • Melting Point 57ºC
  • Formula C15H12
  • Boiling Point 338.8 °C at 760 mmHg
  • Molecular Weight 192.26
  • Flash Point 157.5 °C
  • Transport Information
  • Appearance white Crystalline solid
  • Safety Mutation data reported. When heated to decomposition it emits acrid smoke and irritating vapors.
  • Risk Codes
  • Molecular Structure Molecular Structure of 2531-84-2 (2-METHYLPHENANTHRENE)
  • Hazard Symbols
  • Synonyms 2-Methylphenanthrene;NSC 89276
  • PSA 0.00000
  • LogP 4.30140

2-Methylphenanthrene Chemical Properties

IUPAC Name: 2-Methylphenanthrene 
Molecular Formula: C15H12
Molecular Weight: 192.27g/mol
EINECS: 219-791-0
Density: 1.105 g/cm3
Melting Point :57 °C
Boiling Point: 338.8 °C at 760 mmHg
Flash Point: 157.5 °C
Appearance: white crystalline solid
Freely Rotating Bonds: 0 
Polar Surface Area: 0 Å2 
Index of Refraction: 1.693 
Molar Refractivity: 66.76 cm3 
Molar Volume: 173.9 cm3 
Polarizability: 26.46 ×10-24 cm3 
Surface Tension: 45.8 dyne/cm 
Enthalpy of Vaporization: 55.91 kJ/mol 
Vapour Pressure: 0.000189 mmHg at 25°C 
Solubility: Insoluble in water.
 2-Methylphenanthrene ,its Cas Register Number is 2531-84-2.The chemical synonyms of 2-Methylphenanthrene (CAS No.2531-84-2) are 2-Methyl-phenanthren ; 2-Methylphenanthrene ; Phenanthrene .The molecular structure of 2-Methylphenanthrene (CAS No.2531-84-2) is .

2-Methylphenanthrene Toxicity Data With Reference

1.    

mma-sat 10 µg/plate

    MUREAV    Mutation Research. 156 (1985),61.

2-Methylphenanthrene Safety Profile

Mutation data reported. When heated to decomposition it emits acrid smoke and irritating vapors.

2-Methylphenanthrene Specification

  2-Methylphenanthrene  (CAS No.2531-84-2) vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as 2-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. It may be sensitive to prolonged exposure to light.

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