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CAS No 66-27-3 , methyl methanesulfonate Search by region : Germany

  • Name: methyl methanesulfonate
  • Synonyms: Methanesulfonic acid methyl ester; Methanesulfonic acid; methylmethane sulfonate;Methyl mesylate; methyl ester; 66-27-3;methyl methanesulfonate;
  • CAS Registry Number:
  • Transport: UN 2810
  • Melting Point: 20 C
  • Flash Point: 104 ºC
  • Boiling Point: 202-203 ºC
  • Density: 1.3
  • Refractive index: 1.413-1.415
  • Water Solubility: 200 G/L (20 ºC)
  • Safety Statements: R22;R36/37/38;R45;R68
  • Hazard Symbols: T: Toxic;
  • Flash Point: 104 ºC
  • EINECS: 200-625-0
  • Molecular Weight: 110.13224
  • InchiKey: MBABOKRGFJTBAE-UHFFFAOYSA-N
  • InChI: InChI=1S/C2H6O3S/c1-5-6(2,3)4/h1-2H3
  • Risk Statements: S26;S36/37/39;S45;S53
  • Molecular Formula: C2H6O3S
  • Molecular Structure:CAS No:66-27-3 methyl methanesulfonate

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66-27-3 METHANESULFONIC ACID METHYL ESTER; 98%

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References of methyl methanesulfonate
Title: Methyl Methanesulfonate
CAS Registry Number: 66-27-3
CAS Name: Methanesulfonic acid methyl ester
Synonyms: methyl methanesulfonic acid; as-dimethyl sulfite; methyl mesylate; MMS
Molecular Formula: C2H6O3S
Molecular Weight: 110.13
Percent Composition: C 21.81%, H 5.49%, O 43.58%, S 29.12%
Line Formula: CH3SO2OCH3
Literature References: Prepn: A. Arbusow, P. Pischtschimuka, Chem. Zentralbl. II, 685 (1909); W. E. Bissenger et al., J. Am. Chem. Soc. 70, 3940 (1948). Metabolism: E. A. Barnsley, Biochem. J. 106, 18p (1968). Mutagenicity studies: U. H. Ehling et al., Mutat. Res. 5, 417 (1968); J. Moutschen, ibid. 8, 581 (1969). Review of carcinogenicity studies: IARC Monographs 7, 253-260 (1974). Review of comparative mutagenicity of MMS and ethyl methanesulfonate, q.v.: S. Kondo, Environ. Sci. Res. 24, 743-785 (1981).
Properties: Liquid, bp753 203°, bp0.6 59°. d420 1.2943; nD20 1.4140. Soly in water about 1:5, in DMF about 1:1. Slightly sol in nonpolar solvents.
Boiling point: bp753 203°; bp0.6 59°
Index of refraction: nD20 1.4140
Density: d420 1.2943
CAUTION: This substance is reasonably anticipated to be a human carcinogen: Report on Carcinogens, Eleventh Edition (PB2005-104914, 2004) p III-171.
Use: Exptlly as mutagen, teratogen, brain carcinogen.