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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
- #REDIRECT[[Amine gas treating]]31 bytes (4 words) - 13:20, 9 August 2008
- 12 bytes (1 word) - 11:29, 29 February 2008
- 164 bytes (23 words) - 18:51, 14 June 2008
- 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
- ..., 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
- 1 KB (213 words) - 17:35, 7 February 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
- ...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
- ...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
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) - 13:20, 9 August 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
- ...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
- ...used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.138 bytes (19 words) - 11:33, 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.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
- {{r|Biogenic amine receptor}}639 bytes (81 words) - 19:45, 11 January 2010
- ...mistry]], '''methylenetetrahydrofolate reductase''' is a "[[flavoprotein]] amine oxidoreductase that catalyzes the reversible conversion of [[5-methyltetrah846 bytes (93 words) - 23:50, 16 November 2008
- ===Tertiary amine tricyclics=== ...include [[amitriptyline]], [[doxepin]], and [[imipramine]] have a tertiary-amine side chain block both [[serotonin]] and [[norepinephrine]] and increase [[p5 KB (622 words) - 14:32, 2 February 2023
- {{r|Biogenic amine receptor}}657 bytes (82 words) - 18:58, 11 January 2010
- {{r|Amine}}850 bytes (113 words) - 04:59, 4 August 2009
- {{r|Amine}}602 bytes (81 words) - 19:38, 11 January 2010
- {{r|Amine gas treating}}837 bytes (108 words) - 09:39, 6 March 2024
- ...s''' are "a group of membrane transport proteins that transport [[biogenic amine]] derivatives of catechol across the plasma membrane. Catecholamine plasma706 bytes (82 words) - 05:29, 30 September 2009
- {{r|Biogenic amine receptor}}885 bytes (112 words) - 17:13, 11 January 2010
- {{r|Biogenic amine receptor}}918 bytes (116 words) - 14:21, 8 March 2024
- {{r|Amine gas treating}} {{r|Amine}}3 KB (351 words) - 21:51, 16 August 2010
- In [[pharmacology]], '''tiotropium''' is a derivative of the quaternary amine [[scopolamine]] and is classified as a [[parasympatholytic]], [[cholinergic878 bytes (104 words) - 14:51, 23 June 2011
- {{r|amine}}738 bytes (114 words) - 20:53, 18 March 2011
- {{r|Amine gas treating}}809 bytes (98 words) - 00:31, 31 January 2010
- *Nitriles are reduced to [[amine|amines]] by [[hydrogen]] and a [[nickel]] catalyst827 bytes (113 words) - 17:46, 28 October 2010
- {{r|Biogenic amine receptor}}1,006 bytes (130 words) - 10:50, 11 January 2010
- ...those impurities to acceptable levels, commonly by an [[Amine gas treating|amine gas treater]] or similar process.<ref name=NatGasOrg/><ref>[http://www.eia.3 KB (430 words) - 09:44, 6 March 2024
- {{r|Biogenic amine receptor}}1 KB (148 words) - 16:03, 11 January 2010
- {{r|Biogenic amine receptor}}1 KB (148 words) - 16:21, 11 January 2010
- ...st, a copper(I) cocatalyst, and an excess of a secondary or tertiary alkyl amine. This reaction has proven to be extremely valuable for many multi-component1 KB (156 words) - 18:22, 20 December 2007
- {{r|Biogenic amine receptor}}1 KB (160 words) - 13:27, 17 May 2016
- {{r|Biogenic amine receptor}}1 KB (165 words) - 08:37, 18 June 2008
- ...transamination reaction in which [[glutamic acid|glutamate]] transfers an amine group, becoming <math>\alpha</math>-ketoglutarate in the process, to 3-phos1 KB (181 words) - 08:52, 8 June 2009
- ...see [[antipsychotic agent]]s) which are in turn associated with [[Biogenic amine receptor|dopaminergic receptor]] blockade in the [[basal ganglia]] and [[hy Blockade of the [[Biogenic amine receptor|D2 receptors]], which may be predisposed by genetic polymorphisms4 KB (456 words) - 11:33, 21 June 2008
- ...formula is C<small>10</small>H<small>15</small>N. Methamphetamine is an [[amine]] derivative of [[amphetamine]].2 KB (217 words) - 19:18, 10 November 2007
- ...e alpha carbon and the backbone nitrogen atom, the nitrogen is a secondary amine, making proline an ''imino acid'' rather than an ''amino acid''. However,1 KB (231 words) - 08:46, 8 June 2009
- {{r|Biogenic amine receptor}}2 KB (265 words) - 10:53, 11 January 2010
- ...ne]] and [[serotonin]], adrenergic update inhibitors may overcome the mono-amine deficiency.<ref name="isbn0-07-145153-6">{{cite book |author=Katzung, Bertr2 KB (209 words) - 07:51, 9 September 2009
- ...led trial]] concluded that there was no difference between the biogenic [[amine]]s [[norepinephrine]] (plus [[dobutamine]] as needed for [[cardiac output]]2 KB (294 words) - 02:24, 11 June 2010
- * [[Promethazine]] is a "phenothiazine derivative with histamine [[Biogenic amine receptor|H1]]-blocking, antimuscarinic, and sedative properties. It is used2 KB (276 words) - 22:21, 2 December 2008
- * [[Amine]]s: [[Amine#Synthesis|preparation]] - [[Amine#Reactions|reactions]]9 KB (1,149 words) - 07:52, 2 September 2008
- ...urface receptors}}</ref> Examples are [[neurotransmitter]]s and [[biogenic amine receptor]]s.2 KB (273 words) - 11:27, 4 May 2010
- ...O<sub>2</sub> giving it a molecular mass of 159.23 g/mol. It is both an [[amine]] and a [[carboxylic acid]].2 KB (306 words) - 14:40, 13 February 2011
- ...those impurities to acceptable levels and this is commonly done with an [[amine gas treating]] process.<ref>[http://www.naturalgas.org/naturalgas/processin2 KB (360 words) - 08:07, 15 March 2024
- * [[Rimantadine]] - a cyclic amine derivate of adamantane, inhibits replication of influenza A, but not B.3 KB (321 words) - 05:33, 10 September 2009
- ...beled compounds it was demonstrated that N1 of [[purine]]s arises from the amine group of [[Aspartic acid|Asp]]; C2 and C8 originate from formate; N3 and N92 KB (369 words) - 12:23, 5 January 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
- ...are shown here rather that the deprotonated acid functions and protonated amine groups. }}3 KB (430 words) - 08:08, 8 June 2009
- :For more information, see: [[Hydrodesulfurization]], [[Amine gas treating]], and [[Merox]] ...m petroleum refining and [[natural gas processing]] plants (which also use amine gas treating units to remove hydrogen sulfide from the raw [[natural gas]])9 KB (1,344 words) - 09:37, 6 March 2024
- ...ator vessel is recycle gas which is routed through an [[amine gas treating|amine contactor]] for removal of the reaction product hydrogen sulfide gas (H<sub ...ed as refinery fuel gas. The hydrogen sulfide removed and recovered by the amine gas treating unit is subsequently converted to elemental sulfur in a [[Clau15 KB (2,156 words) - 09:37, 6 March 2024
- ...ator vessel is recycle gas which is routed through an [[amine gas treating|amine contactor]] for removal of the reaction product hydrogen sulfide gas (H<sub ...ed as refinery fuel gas. The hydrogen sulfide removed and recovered by the amine gas treating unit is subsequently converted to elemental sulfur in a [[Clau15 KB (2,197 words) - 09:37, 6 March 2024
- ...ntaining the absorbed hydrogen sulfide) is typically routed to a central [[amine gas treating]] unit elsewhere in the refinery. .... The resulting vapor (referred to as ''offgas'') is routed to a central [[amine gas treating]] unit elsewhere in the refinery. The hydrocracked the endprod17 KB (2,523 words) - 09:37, 6 March 2024
- :For more information, see: [[Hydrodesulfurization]], [[Amine gas treating]], and [[Merox]] ...m petroleum refining and [[natural gas processing]] plants (which also use amine gas treating units to remove hydrogen sulfide from the raw [[natural gas]])10 KB (1,443 words) - 09:37, 6 March 2024
- ...other industries. The absorption processes used for that purpose include [[amine gas treating]], [[Rectisol]] and [[Selexol]] to name a few. ...able below provides typical analyses of the Claus feed gases obtained from amine gas treating and from sour water stripping:13 KB (1,990 words) - 09:37, 6 March 2024
- ...removed from the natural gas by reacting with the ethanolamine (see the [[Amine gas treating]] and [[Natural gas processing]] articles). Another example is4 KB (618 words) - 01:55, 14 March 2024
- ...mically and in an environmentally friendly manner, by reacting a secondary amine, propargyl halides and an azide together in water, under atmospheric oxygen3 KB (437 words) - 14:16, 6 February 2010
- ...reactions occur with [[alcohol|alcohols]], aldehydes, [[amide|amides]], [[amine|amines]], [[azo-comound|azo-compounds]], [[carbamate|carbamates]], caustics4 KB (532 words) - 23:27, 20 February 2010
- ...The alcohol has the higher [[atomic number]], and takes priority over the amine. The suffix for an alcohol ends in "ol", so that the suffix is "anol". #The amine group is not on the carbon with the OH (the #1 carbon), but one carbon over25 KB (3,880 words) - 09:42, 28 September 2013
- ...mically and in an environmentally friendly manner, by reacting a secondary amine, propargyl halides and an azide together in water, under atmospheric oxygen3 KB (477 words) - 13:01, 11 June 2009
- ...nin availability in the [[central nervous system]] (CNS) at the [[Biogenic amine receptor|serotonin 1A receptor]]."<ref>{{MeSH}}</ref><ref name="pmid15784664 KB (592 words) - 19:49, 16 August 2016