𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reversed Phase High Performance Liquid Chromatographic Separation of Esterquats with Indirect Spectrophotometric Detection

✍ Scribed by Yongsoon Chung; Sanghyun Park


Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
213 KB
Volume
60
Category
Article
ISSN
0026-265X

No coin nor oath required. For personal study only.

✦ Synopsis


The reversed phase high performance liquid chromatographic (RP-HPLC) elution behavior of the basic esters and esterquats is discussed with data from indirect spectrophotometric detection. Three kinds of basic esters were synthesized by esterification of triethanolamine (TEA) with palmitic acid of three mole ratios (1:1.35, 1:2.00, and 1:3.00). Esterquats were prepared from quaternization of the basic esters with dimethyl sulfate (DMS). As a result, it was found that capacity factor (kЈ) values of mono-, di-, and triester of the basic esters and esterquats were significantly increased and the elution order reversed as the percentage of 1-propanol (1-PrOH) in mobile phase is increased from 75% to 80%. The RP-HPLC separation and determination of the basic esters and esterquats were also accomplished. Tetraphenylphosphonium bromide (TPPBr) was used as the detection reagent.


πŸ“œ SIMILAR VOLUMES


Chromatographic performance of deuterate
✍ Jinno, K. πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 252 KB πŸ‘ 1 views

The chromatographic performance of the deuterated solvents, CD30D and D20, has been investigated in reversed-phase micro high performance liquid chromatography. The chrornatographic performanceof CD30D is only slightlysuperior to that of CH30H. However, the performance of D20 is significantly superi

Use of binary and ternary mobile phases
✍ WΕ‚adysΕ‚aw GoΕ‚kiewicz; Anna BΕ‚aΕΌewicz; Dariusz Matosiuk πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 465 KB

## Abstract The influence of the nature of typical organic modifiers, used in reversed‐phase systems diluted with water, on retention and selectivity of chiral acetylated diamines and acetonitriles possessing pharmacological activity was investigated. Linear, semilogarithmic relationships between t