Search results

...e, to chemically stable carboxylic acids. Left untreated, these sugars and amines would eventually frustrate crystallization of the sucrose.

[[Category:Amines]]

[[Category:Amines]]

[[Category:Aromatic amines]]

...e primary source of NOCs in the human diet is the nitrosation of secondary amines and amides by nitrites present in food. However, epidemiological studies ca :R₂NH (amines) + NaNO₂ (sodium nitrite) → R₂N-N=O (nitrosamine)

[[Category:Aromatic amines]]

[[Category:Amines]]

[[Category:Amines]]

[[Category:Aromatic amines]]

[[Category:Amines]]

[[Category:Sympathomimetic amines]]

...igands. EDTA^4- usually binds to a metal cation through its two amines and four carboxylates. Many of the resulting [[complex (chemistry)|coordin [[Category:Amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

...hemists from Vitae Pharmaceuticals has developed orally bioavailable alkyl amines based solely on a computational structure-based design (molecule d)<ref nam

[[Category:Amines]]

'''Primary aromatic amines''' (PAA) are a group of compounds. They might be added to [[plastic]]s duri ...om_black_nylon_cooking_utentils_2004.pdf An acute case of primary aromatic amines migrating from cooking utensils]'', Memorandum for the Danish Veterinary an

...id forms water-soluble salts with monovalent cations, low molecular weight amines, and quaternary ammonium compounds. It becomes water-insoluble in the prese

...cracker mixed C4s (after the stream is Merox treated to remove sulfur and amines, and contain 1-butene, 2-butene and isobutylene. Ethylene steam cracker C4

...into the cell via [[endocytosis]]. Once inside the cell protonation of the amines results in an influx of counter-ions and a lowering of the osmotic potentia

...J. Bacteriol.|volume=172|pages=5650–5654}}</ref> This is because charged amines interact with negative charges on the cell membrane, and can cause leakage

...s in the manufacture of precursors to [[polyurethane]]. Like most volatile amines, it possesses the somewhat unpleasant odour of rotten fish. It ignites read ...e]]s such as aniline are, in general, much weaker bases than [[aliphatic]] amines because of the electron-withdrawing effect of the phenyl group. Aniline rea

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

...due to oxidized impurities.<ref name=Ullmann>P. F. Vogt, J. J. Gerulis, “Amines, Aromatic” in Ullmann’s Encyclopedia of Industrial Chemistry 2005, Wile [[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

...ties in common with other aryl (often incorrectly referred to as aromatic) amines. Due to the amino group bonded to the aromatic ring, the toluidines are [[ [[Category:Aromatic amines]]

[[Category:Amines]] [[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Amines]] [[Category:Aromatic amines]]

Aromatic amines, when protonated, usually have lower pKa's (are more acidic) than their non [[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]] [[Category:Amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

...y amine]]; by the condensation of ''para''-aminoazo compounds with primary amines, and by the action of ''para''-nitrosodialkylanilines with secondary [[base [[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines|Naphthylamine, 1-]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

[[Category:Aromatic amines]]

===Adding ammonia and amines=== Similarly proceed the reactions with primary and secondary amines:

...tical workers (drugs, enzymes), seafood processors, shellac handlers (e.g. amines), solderers and refiners (metals), spray painters, insulation installers, p

...Kadlubar FF, Kulldorff M, ''et al.'' |title=Dietary intake of heterocyclic amines and benzo(a)pyrene: associations with pancreatic cancer |journal=Cancer Epi

.... Hydrogen-bonds are formed between the three hydrogen atoms of protonated amines and three oxygen atoms of 18-crown-6. These hydrogen-bonds make the complex

[[Category:Amines]]

[[Category:Amines]]

[[Category:Amines]]

...me=Ullmann>Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-V ...ldehyde]]s and [[ketone]]s. Because of its bifunctional nature, having two amines, it readily forms heterocycles such as [[imidazolidine]]s. Ethylenediamine

[[Category:Amines]]

[[Category:Amines]]

Other [[dithiocarbamate]]s can be prepared similarly from secondary amines and carbon disulfide. They are used as [[chelating agents]] for transition

...It is soluble in polar solvents and exhibits the reactivity of typical for amines. The branched [[isomer]] N(CH₂CH₂NH₂)<sub ...me=Ullmann>Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-V

*Precursor to related imino ligands: Acetylacetone condenses with amines to give, successively, the mono- and the di-[[diketimine]]s wherein the O a

[[Category:Amines]]

[[Category:Amines]]

...igands. EDTA^4- usually binds to a metal cation through its two amines and four carboxylates. Many of the resulting [[complex (chemistry)|coordin [[Category:Amines]]

* Very lipophilic amines that do not easily dissolve in the aqueous phase in their charged form, e.g * Lower amines like [[ammonia]], [[methylamine]], or [[triethanolamine]] which are miscibl

...]], but Pd²⁺ forms stronger complexes with phosphines than with amines. Later, Pearson proposed the theory of [[HSAB theory|hard and soft acids an

Virtually all ligands are known to bridge, with the exception of amines and ammonia.<ref>{{cite journal | last = Werner | first = H. | year = 2004

...-David, Y. and Milstein, D., "Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂", Science, 2007, 317, 790-792.{{doi|10.112

...wiki></sup>, when it is sexidentate, binds as a κ⁶-ligand, the amines and the carboxylate oxygen atoms are not contiguous. In practice, the n val

[[Category:Amines]]

...singlet ground-state; that is, they have lone electron pairs (e.g. water, amines, ethers), so these substrates need an empty orbital to be able to react wit

...f coordination compounds. Octahedral transition-metal complexes containing amines and simple anions are often referred to Werner-type complexes.

[[Category:Aromatic amines]]

[[Category:Biogenic amines]]

[[Category:Amines]]

[[Category:Amines]]

[[Category:Amines]]

[[Category:Aromatic amines]]

...[tyramine]]. Some aged cheeses contain significant concentrations of these amines, which can trigger symptoms mimicking an [[allergic reaction]]: [[headache]

...Kerstin Skog, Håkan Olsson, Elisabet Wirfält |title=Do both heterocyclic amines and omega-6 polyunsaturated fatty acids contribute to the incidence of brea