Phenol, 3-pentadecyl-

• Formula: C₂₁H₃₆O
• Molecular weight: 304.5099
• IUPAC Standard InChI: InChI=1S/C21H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-20-17-15-18-21(22)19-20/h15,17-19,22H,2-14,16H2,1H3 Copy

  
• IUPAC Standard InChIKey: PTFIPECGHSYQNR-UHFFFAOYSA-N Copy
• CAS Registry Number: 501-24-6
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Phenol, m-pentadecyl-; m-Pentadecylphenol; Anacardol, tetrahydro-; Cyclogallipharaol; Hydrocardanol; Hydroginkgol; Tetrahydroanacardol; 3-n-Pentadecylphenol; 3-Pentadecylphenol; Cardolite NC-507; NSC 9781; Cardolite NC-510
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Reduced pressure boiling point

Enthalpy of fusion

IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Gas Phase Spectrum

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Additional Data

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Van Den Dool and Kratz RI, non-polar column, custom temperature program

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Loev and Dawson, 1956
Loev, B.; Dawson, C.R., Synthesis of the Mone- and Dihydric Pentadecylphenols Related to Poison Ivy Urushiol, J. Am. Chem. Soc., 1956, 78, 5083-6. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Mao, Luo, et al., 2010
Mao, Zhi-Bo; Luo, Ting-Liang; Cui, Tie-Bing; Wang, Yu; Liu, Guo-Ji, Solubilities of 3-Pentadecylphenol in Ethanol, 1-Butanol, Toluene, Acetone, Tetrachloromethane, and Ethyl Acetate, J. Chem. Eng. Data, 2010, 55, 1, 543-546, https://doi.org/10.1021/je900346t . [all data]

Andriamaharavo, 2014
Andriamaharavo, N.R., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2014. [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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