Dichlorophen

• Formula: C₁₃H₁₀Cl₂O₂
• Molecular weight: 269.123
• IUPAC Standard InChI: InChI=1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2 Copy

  
• IUPAC Standard InChIKey: MDNWOSOZYLHTCG-UHFFFAOYSA-N Copy
• CAS Registry Number: 97-23-4
• 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, 2,2'-methylenebis[4-chloro-; Anthiphen; Antifen; Bis(chlorohydroxyphenyl)methane; Bis(2-hydroxy-5-chlorophenyl)methane; Bis(5-chloro-2-hydroxyphenyl)methane; Cordocel; Dicestal; Dichlorofen (Czech); Dichlorophen B; Dichlorophene; Dichlorophene 10; Dichlorphen; Didroxan; Didroxane; Difentan; Diphentane 70; Diphenthane 70; DDDM; DDM; Embephen; Fungicide GM; Fungicide M; G 4; G-4 Pure; G-4 Technical; Gefir; Gingivit; GH; Halenol; Hyosan; Korium; Palacel; Panacide; Parabis; Plath-Lyse; Prevental; Preventol GD; Preventol GDC; Taeniatol; Teniathane; Teniatol; Teniotol; Vermithana; 2,2'-Dihydroxy-5,5'-dichlorodiphenylmethane; 2,2'-Methylenebis[4-chlorophenol]; Antiphen; Bis(5-chlor-2-hydroxyphenyl)-methan; Bis-2-hydroxy-5-chlorfenylmethan; Di-(5-chloro-2-hydroxyphenyl)methane; Dichloorfeen; Dichlorofen; Methanedichlorofen; O,O-Methyleen-bis-(4-chloorfenol); O,O-Metilen-bis(4-cloro-fenolo); Trivex; 5,5'-Dichloro-2,2'-dihydroxydiphenylmethane; 4,4'-Dichloro-2,2'-methylenediphenol; Fungicide FX; Preventol; Super mosstox; Wespuril; Acticide DDM; Algafen; Algofen; Anthipen; Nuophene; Westpuril; Sandocide; Giv Gard G 4-40
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• Information on this page:
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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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: Coblentz Society, Inc.

Condensed Phase Spectrum

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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

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, temperature ramp

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Normal alkane 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.

Perrigo and Peel, 1981
Perrigo, B.J.; Peel, H.W., The use of retention indices and temperature-programmed gas chromatography in analytical toxicology, J. Chromatogr. Sci., 1981, 19, 5, 219-226, https://doi.org/10.1093/chromsci/19.5.219 . [all data]

Ardrey and Moffat, 1981
Ardrey, R.E.; Moffat, A.C., Gas-liquid chromatographic retention indices of 1318 substances of toxicological interest on SE-30 or OV-1 stationary phase, J. Chromatogr., 1981, 220, 3, 195-252, https://doi.org/10.1016/S0021-9673(00)81925-1 . [all data]

Notes

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