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- ...queous solutions of various [[alkanol]]s (commonly referred to as simply [[amine]]s) to remove [[hydrogen sulphide]] (H<sub>2</sub>S) and [[carbon dioxide]] ==Description of a typical amine treater==9 KB (1,470 words) - 09:37, 6 March 2024
- ...weetening.aspx Amine Sweetening] (A goodly number of published articles on amine sweetening]853 bytes (115 words) - 17:19, 7 February 2008
- 855 bytes (137 words) - 23:23, 15 July 2008
- 393 bytes (48 words) - 09:39, 6 March 2024
- [[Category:CZ Authors|Ramdani El Khafif, Ahmed Amine]] [[Category:Economics Authors|Ramdani El Khafif, Ahmed Amine]]654 bytes (95 words) - 02:57, 22 November 2023
- 116 bytes (13 words) - 08:08, 20 July 2021
Page text matches
- A process using aqueous solutions of [[amine]]s to remove [[hydrogen sulphide]] (H<sub>2</sub>S) and [[carbon dioxide]]187 bytes (28 words) - 09:37, 6 March 2024
- A group of membrane transport proteins that transport biogenic amine derivatives of catechol across the plasma membrane.157 bytes (20 words) - 05:50, 30 September 2009
- Auto-populated based on [[Special:WhatLinksHere/Amine]]. Needs checking by a human. {{r|Amine gas treating}}881 bytes (116 words) - 10:53, 11 January 2010
- A biogenic amine involved in local immune responses as well as regulating physiological func178 bytes (25 words) - 20:24, 3 September 2009
- ...reagent used to couple [[carboxylic acid]]s with either [[alcohol]]s or [[amine]]s to form [[ester]]s or [[amide]]s.288 bytes (35 words) - 11:03, 3 October 2009
- ....png|left|350px|'''Scheme 1''':Coupling of a carboxylic acid and a primary amine via O-acylisourea ester and NHS ester intermediates.}} ...compound that remains reactive with amines. Upon the final addition of an amine ('''6'''), the final desired coupling product, an amide ('''7'''), is forme1 KB (235 words) - 10:55, 9 January 2010
- ...xylic acids]]. While these appear to contain a [[carbonyl]] bonded to an [[amine]], their reactivity is very different from either of those two [[functional ...arboxylic acid]] derivatives with ammonia, a primary amine, or a secondary amine will give an amide. By using derivatives of other acids [such as sulfuric],3 KB (410 words) - 02:51, 17 October 2013
- {{r|Amine gas treating}}247 bytes (29 words) - 09:39, 6 March 2024
- ...o activate [[carboxylic acid]]s for coupling with either [[alcohol]]s or [[amine]]s to form [[ester]] or [[amide]] products. It is similar to [[N,N'-dicycl453 bytes (63 words) - 11:31, 3 October 2009
- {{r|Amine gas treating}}290 bytes (33 words) - 09:52, 6 March 2024
- {{r|amine}}178 bytes (23 words) - 16:09, 4 November 2010
- {{r|Amine gas treating}}295 bytes (35 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}295 bytes (35 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}473 bytes (56 words) - 17:48, 16 June 2010
- {{r|Amine gas treating}}354 bytes (43 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}462 bytes (56 words) - 12:12, 18 March 2012
- {{r|Amine gas treating}}456 bytes (53 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}449 bytes (56 words) - 03:48, 1 March 2011
- ...ylic acid]]s for subsequent coupling with either [[alcohol]]s or primary [[amine]]s to form [[ester]]s or [[amide]]s. It is a [[carbodiimide]] type of reag511 bytes (72 words) - 14:17, 19 June 2024
- {{r|Amine gas treating}}379 bytes (49 words) - 09:27, 6 March 2024