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CAS No 1921-70-6 , 2,6,10,14-tetramethylpentadecane

  • Name: 2,6,10,14-tetramethylpentadecane
  • Synonyms: Bute hydrocarbon; Pristan; Norphytan; 1921-70-6; Norphytane; 2,6,10,14-tetramethyl-;2,6,10,14-tetramethylpentadecane; Pentadecane; 2,6,10,14-Tetramethylpentadecane;
  • CAS Registry Number:
  • Melting Point: -99 °C
  • Flash Point: 110 °C
  • Boiling Point: 68 °C0.001 mm Hg(lit.)
  • Density: 0.783 g/mL at 20 °C(lit.)
  • Refractive index: 20/D 1.438(lit.)
  • Safety Statements: Questionable carcinogen with experimental neoplastigenic and tumorigenic data. A severe skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
  • Hazard Symbols: Xi
  • Flash Point: 110 °C
  • EINECS: 217-650-8
  • Molecular Weight: 268.5209
  • InchiKey: XOJVVFBFDXDTEG-UHFFFAOYSA-N
  • InChI: InChI=1S/C19H40/c1-16(2)10-7-12-18(5)14-9-15-19(6)13-8-11-17(3)4/h16-
    19H,7-15H2,1-6H3
  • Risk Statements: 36/38
  • Molecular Formula: C19H40
  • Molecular Structure:CAS No:1921-70-6 2,6,10,14-tetramethylpentadecane
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1921-70-6 2,6,10,14-TETRAMETHYLPENTADECANE

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
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1921-70-6 0635.19-K-IO 2,6,10,14-TETRAMETHYLPENTADECANE

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1921-70-6 2,6,10,14-TETRAMETHYLPENTADECANE

  • Germany AppliChem GmbH [Manufacturer]
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1921-70-6 8663.00 2,6,10,14-TETRAMETHYLPENTADECANE

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1921-70-6 2,6,10,14-Tetramethylpentadecane

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1921-70-6 2,6,10,14-Tetramethylpentadecane

  • China Hong Kong Beautart Biochem Co., Ltd. null
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References of 2,6,10,14-tetramethylpentadecane
Title: Pristane
CAS Registry Number: 1921-70-6
CAS Name: 2,6,10,14-Tetramethylpentadecane
Synonyms: norphytane
Trademarks: Robuoy (Robeco)
Molecular Formula: C19H40
Molecular Weight: 268.52
Percent Composition: C 84.99%, H 15.01%
Literature References: Isoprenoid alkane obtained from the unsaponifiable fraction of shark liver oil where it occurs to an extent of 14%: Tsujimoto, J. Soc. Chem. Ind. 51, 317T (1932); S?rensen, Mehllum, Acta Chem. Scand. 2, 140 (1948). Identity with norphytane: Pliva, S?rensen, ibid. 4, 846 (1950). Isoln from petroleum crude oils: Bendoraitis et al., Anal. Chem. 34, 49 (1962); from wool wax: Mold et al., Nature 199, 283 (1963). Synthesis from phytol: S?rensen, S?rensen, Acta Chem. Scand. 3, 939 (1949). Metabolism: McKenna, Kallio, Proc. Natl. Acad. Sci. USA 68, 1552 (1971). Use in inducing murine plasmacytomas: P. N. Anderson, M. Potter, Nature 222, 994 (1969). Effect on ascites tumor formation and monoclonal antibody production: N. J. Hoogenraad, C. J. Wraight, Methods Enzymol. 121, 375 (1986).
Properties: Mobile, transparent, stable liq. d420 0.78267. Congealing point -100°. bp760 296°; bp10 158°; bp0.001 68° (bath temp). nD20 1.43848. Acid no. 0-5. Iodine no. 0-7.5. Sapon no. 0-5. Viscosity at 25°: 5 cP. Soluble in ether, petr ether, benzene, chloroform, carbon tetrachloride.
Boiling point: bp760 296°; bp10 158°; bp0.001 68° (bath temp)
Index of refraction: nD20 1.43848
Density: d420 0.78267
Use: Lubricant; transformer oil. Anti-corrosion agent. Biological marker. In experimental systems to induce plasmacytomas; in production of monoclonal antibodies.