Chlorpromazine

• Formula: C₁₇H₁₉ClN₂S
• Molecular weight: 318.864
• IUPAC Standard InChI: InChI=1S/C17H19ClN2S/c1-19(2)10-5-11-20-14-6-3-4-7-16(14)21-17-9-8-13(18)12-15(17)20/h3-4,6-9,12H,5,10-11H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: ZPEIMTDSQAKGNT-UHFFFAOYSA-N Copy
• CAS Registry Number: 50-53-3
• Chemical structure:
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• Other names: 10H-Phenothiazine-10-propanamine, 2-chloro-N,N-dimethyl-; Phenothiazine, 2-chloro-10-[3-(dimethylamino)propyl]-; Aminazin; Aminazine; Ampliactil; Amplictil; Chlor-Promanyl; Chlorderazin; Chlorpromados; Contomin; CPZ; Elmarin; Esmind; Fenactil; Fenaktyl; Fraction AB; HL 5746; Largactil; Largactilothiazine; Largactyl; Megaphen; Novomazina; Phenactyl; Plegomasine; Proma; Promactil; Promazil; Propaphenin; Prozil; Sanopron; SKF 2601-A; Thorazine; Torazina; Wintermin; 2-Chloro-10-[3-(Dimethylamino)propyl]phenothiazine; 2-Chloropromazine; 4560 R.P.; Aminasine; Amplicitil; Chloropromazine; Chlorpromazin; Psychozine; 2-Cloro-10 (3-dimetilaminopropil)fenotiazina; Clorpromazina; 2601-A; RP-4560; BC 135
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• Information on this page:
  • Gas phase ion energetics data
  • IR Spectrum
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Gas phase ion energetics 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:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Ionization energy determinations

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

References

Go To: Top, Gas phase ion energetics data, IR Spectrum, Notes

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

Poltorakov, Pirnazarova, et al., 1973
Poltorakov, A.P.; Pirnazarova, F.N.; But, P.G.; Piruzyan, L.A.; Chibrikin, V.M.; Vikjlyaev, Yu.I.; Ul'yanova, O.V., Ionization potentials of phenothiazine derivatives and their correlation with the parmacologic effect, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1973, 22, 2050, In original 2106. [all data]

Fulton and Lyons, 1968
Fulton, A.; Lyons, L.E., The ionization energies of some phenothiazine tranquillizers and molecules of similar structure, Australian J. Chem., 1968, 21, 873. [all data]

Domelsmith, Munchausen, et al., 1977
Domelsmith, L.N.; Munchausen, L.L.; Houk, K.N., Photoelectron spectra of psychotropic drugs. 2. Phenothiazine and related tranquilizers, J. Am. Chem. Soc., 1977, 99, 6506. [all data]

Notes

Go To: Top, Gas phase ion energetics data, IR Spectrum, References

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