10H-Phenothiazin-3-ol, 10-[3-(dimethylamino)propyl]-, acetate (ester)
- Formula: C19H22N2O2S
- Molecular weight: 342.455
- IUPAC Standard InChI: InChI=1S/C19H22N2O2S/c1-14(22)23-15-9-10-17-19(13-15)24-18-8-5-4-7-16(18)21(17)12-6-11-20(2)3/h4-5,7-10,13H,6,11-12H2,1-3H3
- IUPAC Standard InChIKey: WZQPRXUQVBEBTL-UHFFFAOYSA-N
- CAS Registry Number: 56438-23-4
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Prothipendyl M (HO-), monoacetylated; Promazine M (HO-), monoacetylated
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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
Normal alkane RI, non-polar column, temperature ramp
| Column type | Active phase | I | Reference | Comment |
|---|---|---|---|---|
| Packed | OV-101 | 2709. | Maurer and Pfleger, 1984 | N2, Chromosorb G HP, 20. K/min, 310. C @ 3. min; Column length: 0.6 m; Tstart: 100. C |
| Packed | OV-101 | 2781. | Maurer and Pfleger, 1984 | N2, Chromosorb G HP, 20. K/min, 310. C @ 3. min; Column length: 0.6 m; Tstart: 100. C |
References
Go To: Top, Gas Chromatography, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Maurer and Pfleger, 1984
Maurer, H.; Pfleger, K.,
Screening procedure for detection of phenothiazine and analogous neuroleptics and their metabolites in urine using a computerized gas chromatographic-mass spectrometric technique,
J. Chromatogr., 1984, 306, 125-145, https://doi.org/10.1016/S0378-4347(00)80876-2
. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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