Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate
Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Takano, Satoshi [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1983 |
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| Schlagwörter: |
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| Anmerkung: |
© American Oil Chemists’ Society 1983 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of the American Oil Chemists’ Society - Springer-Verlag, 1947, 60(1983), 10 vom: Okt., Seite 1807-1815 |
|---|---|
| Übergeordnetes Werk: |
volume:60 ; year:1983 ; number:10 ; month:10 ; pages:1807-1815 |
| Links: |
|---|
| DOI / URN: |
10.1007/BF02680360 |
|---|
| Katalog-ID: |
OLC2068089491 |
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| 245 | 1 | 0 | |a Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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| 520 | |a Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. | ||
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10.1007/BF02680360 doi (DE-627)OLC2068089491 (DE-He213)BF02680360-p DE-627 ger DE-627 rakwb eng 660 VZ Takano, Satoshi verfasserin aut Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate 1983 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1983 Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant Tsuji, Kazuro aut Enthalten in Journal of the American Oil Chemists’ Society Springer-Verlag, 1947 60(1983), 10 vom: Okt., Seite 1807-1815 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:60 year:1983 number:10 month:10 pages:1807-1815 https://doi.org/10.1007/BF02680360 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_70 GBV_ILN_95 GBV_ILN_252 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 60 1983 10 10 1807-1815 |
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10.1007/BF02680360 doi (DE-627)OLC2068089491 (DE-He213)BF02680360-p DE-627 ger DE-627 rakwb eng 660 VZ Takano, Satoshi verfasserin aut Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate 1983 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1983 Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant Tsuji, Kazuro aut Enthalten in Journal of the American Oil Chemists’ Society Springer-Verlag, 1947 60(1983), 10 vom: Okt., Seite 1807-1815 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:60 year:1983 number:10 month:10 pages:1807-1815 https://doi.org/10.1007/BF02680360 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_70 GBV_ILN_95 GBV_ILN_252 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 60 1983 10 10 1807-1815 |
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10.1007/BF02680360 doi (DE-627)OLC2068089491 (DE-He213)BF02680360-p DE-627 ger DE-627 rakwb eng 660 VZ Takano, Satoshi verfasserin aut Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate 1983 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1983 Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant Tsuji, Kazuro aut Enthalten in Journal of the American Oil Chemists’ Society Springer-Verlag, 1947 60(1983), 10 vom: Okt., Seite 1807-1815 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:60 year:1983 number:10 month:10 pages:1807-1815 https://doi.org/10.1007/BF02680360 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_70 GBV_ILN_95 GBV_ILN_252 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 60 1983 10 10 1807-1815 |
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10.1007/BF02680360 doi (DE-627)OLC2068089491 (DE-He213)BF02680360-p DE-627 ger DE-627 rakwb eng 660 VZ Takano, Satoshi verfasserin aut Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate 1983 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1983 Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant Tsuji, Kazuro aut Enthalten in Journal of the American Oil Chemists’ Society Springer-Verlag, 1947 60(1983), 10 vom: Okt., Seite 1807-1815 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:60 year:1983 number:10 month:10 pages:1807-1815 https://doi.org/10.1007/BF02680360 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_70 GBV_ILN_95 GBV_ILN_252 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 60 1983 10 10 1807-1815 |
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10.1007/BF02680360 doi (DE-627)OLC2068089491 (DE-He213)BF02680360-p DE-627 ger DE-627 rakwb eng 660 VZ Takano, Satoshi verfasserin aut Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate 1983 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1983 Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant Tsuji, Kazuro aut Enthalten in Journal of the American Oil Chemists’ Society Springer-Verlag, 1947 60(1983), 10 vom: Okt., Seite 1807-1815 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:60 year:1983 number:10 month:10 pages:1807-1815 https://doi.org/10.1007/BF02680360 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_70 GBV_ILN_95 GBV_ILN_252 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 60 1983 10 10 1807-1815 |
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660 VZ Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate Diamine Ethyl Acrylate Preparative Thin Layer Chromatography Lithium Aluminum Hydride Amphoteric Surfactant |
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ddc 660 misc Diamine misc Ethyl Acrylate misc Preparative Thin Layer Chromatography misc Lithium Aluminum Hydride misc Amphoteric Surfactant |
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ddc 660 misc Diamine misc Ethyl Acrylate misc Preparative Thin Layer Chromatography misc Lithium Aluminum Hydride misc Amphoteric Surfactant |
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Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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Takano, Satoshi |
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Journal of the American Oil Chemists’ Society |
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1983 |
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Takano, Satoshi Tsuji, Kazuro |
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660 |
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analysis of cationic and amphoteric surfactants: v. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. © American Oil Chemists’ Society 1983 |
| abstractGer |
Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. © American Oil Chemists’ Society 1983 |
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Abstract Structural analysis of the amphoteric surfactants obtained by the reaction of l-(2-hydroxyethyl)-2-alkyl-2-imidazoline (HEAI) with sodium monochloroacetate has been carried out. These amphoteric surfactants were hydrolyzed under aqueous alkaline media, followed by acid hydrolysis to afford fatty acid and diamine derivatives. The resulting diamine derivatives were identified by the isolation and their syntheses, and were quantitatively analyzed by gas chromatography. Based upon the results of these analyses, it has been found that the reaction products can be divided into two typical types. The reaction products have simpler compositions than those of ethyl acrylate. However, these amphoteric surfactants are characterized by the presence of appreciable amounts of hydrolysis products of amides, soap and free diamine derivative XI. © American Oil Chemists’ Society 1983 |
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Analysis of cationic and amphoteric surfactants: V. structural analysis of the amphoteric surfactants obtained by the reaction of 1-(2-Hydroxyethyl)-2-alkyl-2-imidazoline with sodium monochloroacetate |
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