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- ...l is called a primary amine, secondary amine, tertiary amine or quaternary amine, respectively. In [[biochemistry]], amines act on [[biogenic amine receptor]]s.1 KB (198 words) - 22:22, 2 December 2008
- 164 bytes (23 words) - 18:51, 14 June 2008
- #REDIRECT[[Amine gas treating]]31 bytes (4 words) - 13:20, 9 August 2008
- 12 bytes (1 word) - 11:29, 29 February 2008
- ..., and compounds closely related to each of these."<ref name="MeSH-Biogenic amine receptors">{{MeSH}}</ref> [[Histamine]] is an "amine derived by enzymatic decarboxylation of histidine. It is a powerful stimula12 KB (1,572 words) - 08:41, 15 July 2010
- ...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 (1,476 words) - 09:37, 6 March 2024
- 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
- #REDIRECT[[Amine gas treating]]31 bytes (4 words) - 11:26, 6 May 2008
- 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
- 12 bytes (1 word) - 15:16, 23 January 2008
- 1 KB (157 words) - 15:26, 28 September 2009
- 210 bytes (26 words) - 17:06, 14 May 2010
- 1 KB (213 words) - 17:35, 7 February 2008
- ...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
- 855 bytes (137 words) - 23:23, 15 July 2008
- ...weetening.aspx Amine Sweetening] (A goodly number of published articles on amine sweetening]853 bytes (115 words) - 17:19, 7 February 2008
- 393 bytes (48 words) - 09:39, 6 March 2024
Page text matches
- ...l is called a primary amine, secondary amine, tertiary amine or quaternary amine, respectively. In [[biochemistry]], amines act on [[biogenic amine receptor]]s.1 KB (198 words) - 22:22, 2 December 2008
- #REDIRECT[[Amine gas treating]]31 bytes (4 words) - 11:26, 6 May 2008
- #REDIRECT [[Amine gas treating]]32 bytes (4 words) - 13:44, 28 April 2008
- #REDIRECT [[Amine gas treating]]32 bytes (4 words) - 13:44, 28 April 2008
- #Redirect [[Amine gas treating]]32 bytes (4 words) - 20:23, 28 April 2008
- #Redirect [[Amine gas treating]]32 bytes (4 words) - 20:24, 28 April 2008
- #REDIRECT[[Amine gas treating]]31 bytes (4 words) - 13:20, 9 August 2008
- ...weetening.aspx Amine Sweetening] (A goodly number of published articles on amine sweetening]853 bytes (115 words) - 17:19, 7 February 2008
- ...ration reagent]] used to couple [[carboxylic acid]]s with [[alohol]]s or [[amine]]s.129 bytes (18 words) - 11:05, 3 October 2009
- ...drating chemical mostly used to couple [[carboxylic acid]]s with primary [[amine]]s, producing an [[amide]] compound.157 bytes (20 words) - 10:36, 3 October 2009
- ...used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.138 bytes (19 words) - 11:33, 3 October 2009
- ...used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.153 bytes (21 words) - 10:31, 3 October 2009
- ...cal compound with an [[alkene]] group (C=C) next to a [[nitrogen]] atom ([[amine]] form).134 bytes (19 words) - 20:55, 18 March 2011
- 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
- {{r|Amine}}171 bytes (19 words) - 10:33, 3 October 2009
- ...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
- ...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 reag480 bytes (68 words) - 10:12, 13 March 2024
- {{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
- {{r|Amine gas treating}}379 bytes (49 words) - 09:27, 6 March 2024
- {{r|Amine gas treating}}555 bytes (69 words) - 09:39, 6 March 2024
- {{r|Amine}}319 bytes (34 words) - 10:40, 3 October 2009
- ...ed to activate [[carboxylic acid]]s for subsequent coupling with primary [[amine]]s, producing an [[amide]] compound. The carboxyl group is often converted ....png|left|350px|'''Scheme 2''':Coupling of a carboxylic acid and a primary amine via O-acylisourea ester and NHS ester intermediates.}}3 KB (480 words) - 12:22, 27 August 2010
- {{r|Amine gas treating}}532 bytes (68 words) - 09:39, 6 March 2024
- ...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 (1,476 words) - 09:37, 6 March 2024
- ...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
- {{r|Biogenic amine receptor}}491 bytes (62 words) - 10:50, 11 January 2010
- *HN3: Tris(2-chloroethyl)amine (555-77-1)647 bytes (77 words) - 17:05, 22 June 2009
- {{r|Amine}}575 bytes (73 words) - 10:33, 23 March 2024
- {{r|Biogenic amine receptor}}549 bytes (69 words) - 16:47, 11 January 2010
- {{r|Amine}}581 bytes (75 words) - 19:42, 11 January 2010
- {{r|Biogenic amine receptor}}615 bytes (78 words) - 14:03, 1 April 2024
- {{r|Amine}}597 bytes (78 words) - 18:28, 11 January 2010
- {{r|Amine}}549 bytes (72 words) - 19:15, 11 January 2010
- {{r|Biogenic amine receptor}}608 bytes (77 words) - 19:26, 11 January 2010
- {{r|Biogenic amine receptor}}586 bytes (73 words) - 20:18, 11 January 2010