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- Soap consists of sodium or potassium [[salt (chemistry)|salt]]s of fatty acids and is obtained by reacting common oils or fats wit ...p Dispersants, Raymond G. Bistline, Jr., in ''Anionic surfactants: organic chemistry'', Helmut Stache, ed., Volume 56 of Surfactant science series, CRC Press, 120 KB (3,140 words) - 22:41, 17 June 2010
- ...the alkaloid from natural sources. The first synthetic [[organic chemistry|organic]] [[dye]], [[mauveine]], was discovered by [[William Henry Perkin]] in 1856 * [http://www.organic-chemistry.org/Highlights/2004/01November.shtm Catalytic Asymmetric Synthesis of Quini27 KB (3,844 words) - 16:41, 27 September 2010
- Chloramphenicol poisoning can cause sensitivity reactions to organic acids and salicylates. ...hanism of Action of Chloramphenicol ] July 1963. The Journal of Biological Chemistry)</ref>29 KB (3,876 words) - 16:42, 27 September 2010
- ...drazid'''), also known as '''isonicotinylhydrazine''' ('''INH'''), is an [[organic compound]] that is the first-line anti[[tuberculosis]] medication in preven ...ridine and Pyridine Derivatives|title=Ullmann's Encyclopedia of Industrial Chemistry|year=2007|publisher=John Wiley & Sons|location=New York}}{{Page needed|12 KB (1,566 words) - 16:43, 27 September 2010
- ...yday "Iodine and Iodine Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim</ref> ===Inorganic chemistry===23 KB (3,281 words) - 16:44, 27 September 2010
- ...ive research effort between [[Antonín Holý]] at the Institute of Organic Chemistry and Biochemistry, [[Academy of Sciences of the Czech Republic]] (IOCB) in [6 KB (871 words) - 16:45, 27 September 2010
- ...acturing [[azo compound|diazo]] [[dye]]s, [[nitroso compound]]s, and other organic compounds; in dyeing and printing textile fabrics and bleaching fibers; in ...t5 = M.B.P.P. | last6 = Delerue-Matos | first6 = Cristina | journal = Food Chemistry | volume = 120 | pages = 960}}</ref><ref name = Leszczyńska>{{cite journa21 KB (3,046 words) - 16:45, 27 September 2010
- ...known as PAS, is an [[antibiotic]] used to treat [[tuberculosis]]. This [[organic compound]] has been use since the 1940s for the treatment of [[inflammatory ...Waring, R.H. “Aminophenols.” In Ullmann’s Encyclopedia of Industrial Chemistry; 2002 Wiley-VCH, {{DOI|10.1002/14356007.a02_099}}</ref>7 KB (879 words) - 16:46, 27 September 2010
- ...It has many uses in a range of different fields, such as [[biology]] and [[chemistry]]. At room temperature it appears as a solid, odorless, dark green powder, ===Chemistry===27 KB (3,650 words) - 16:46, 27 September 2010
- ...es its only use was in laboratories as a "metabolically inert" solvent for organic compounds. In 1962, the French researcher Pierre Eymard serendipitously dis25 KB (3,328 words) - 16:47, 27 September 2010
- ...he chemical is typically an [[acid]], strong [[Alkali|base]], or a [[Salt (chemistry)|salt]] ([[phosphoric acid]], [[potassium hydroxide]], [[sodium hydroxide]] ...emicals, including [[alcohol]]s, [[glycol]]s, strong [[acid]]s and [[base (chemistry)|bases]], [[metal]]s and most [[inorganic]]s, such as [[lithium]], [[sodiu41 KB (5,738 words) - 16:47, 27 September 2010
- ==Chemistry== ...in undergraduate teaching labs.<ref>{{Cite book|title=Experimental Organic Chemistry |last=Palleros |first=Daniel R. |year=2000 |publisher=John Wiley & Sons|loc78 KB (10,918 words) - 16:52, 27 September 2010
- ...ell. It is a [[weak acid]], in that it is only a partially [[dissociation (chemistry)|dissociated]] acid in an [[aqueous solution]]. Pure, [[water]]-free acetic ...ar = 1917|title = Industrial and Manufacturing Chemistry|edition = Part 1, Organic|location = London|publisher = Crosby Lockwood|pages=330–31}}</ref>41 KB (5,915 words) - 16:49, 27 September 2010
- ...lla|first1=John A.|last2=Tweit|first2=Robert C.|journal=Journal of Organic Chemistry|volume=24|pages=1109}}12 KB (1,555 words) - 16:49, 27 September 2010
- ...5 (β-anomer) <!-- these CAS numbers have been verified against CAS Common Chemistry --> [[Aldohexose]]s have four [[chirality (chemistry)|chiral centers]] in their acyclic forms (i.e. ignoring the anomeric carbon23 KB (3,050 words) - 16:52, 27 September 2010
- ...of Newmarket]]. Mentioned for the Nobel Prize for Scientific Attainment in Chemistry. Prof. George Poe, a cousin of the poet Edgar Allan Poe, a noted scientist ...cial source, but will require the removal of higher oxides of nitrogen and organic impurities. Currently much of the gas is decomposed before release for envi61 KB (8,728 words) - 16:50, 27 September 2010
- ...Why is mercury a liquid at STP?| accessdate=May 1, 2007| publisher=General Chemistry Online at Frostburg State University| author=Senese, F}}</ref><ref name="No ...|title=Why is mercury liquid? Or, why do relativistic effects not get into chemistry textbooks?| journal= Journal of Chemical Education|volume=68|page=110 |year69 KB (10,077 words) - 21:35, 20 September 2010
- ...function of frequency. Lower frequencies are less affected by the [[Salt (chemistry)|salt]], so that the acoustic energy travels much farther in the ocean. [[B ...in organic synthesis due to its affinity for water. During [[work-up]], an organic phase is saturated with magnesium sulfate until it no longer forms clumps.14 KB (1,882 words) - 16:50, 27 September 2010
- ==Chemistry== ...g poppy straw use steam, one or more of several types of alcohol, or other organic solvents.87 KB (12,376 words) - 16:51, 27 September 2010
- '''EDTA''' is a widely used initialism for the [[organic compound]] '''ethylenediaminetetraacetic acid''' (for other names, see Tabl ...Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.{{DOI|10.1002/14356007.a10_095}}</ref>21 KB (2,946 words) - 15:10, 6 July 2010
