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2-furaldehyde
Furfural is an organic compound with the formula C4H3OCHO. It is a colorless liquid, although commercial samples are often brown. It has an aldehyde group attached to the 2-position of furan. It is a product of the dehydration of sugars, as occurs in a variety of agricultural byproducts, including corncobs, oat, wheat bran, and sawdust. The name ''furfural'' comes from the Latin word , meaning bran, referring to its usual source. Furfural is only derived from lignocellulosic biomass, i.e., its origin is non-food or non-coal/oil based. Aside from ethanol, acetic acid, and sugar, it is one of the oldest renewable chemicals. It is also found in many processed foods and beverages. History Furfural was first isolated in 1821 (published in 1832) by the German chemist Johann Wolfgang Döbereiner, who produced a small sample as a byproduct of formic acid synthesis. In 1840, the Scottish chemist John Stenhouse found that the same chemical could be produced by distilling a wide variety of ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Methoxymethylfurfural
Methoxymethylfurfural (MMF or 5-methoxymethylfuran-2-carbaldehyde) is an organic compound derived from dehydration of sugars and subsequent etherification with methanol.van Putten, R-J., van der Waal J.C. de Jong, E., Rasrendra C.B., Heeres, E.J. and de Vries HG. (2011) Furan-based platform chemicals of the future. Dehydration of hexoses as biosustainable product route. Chemical Reviews submitted. This colorless liquid is soluble in a wide range of solvents including lower alcohols. The molecule is a derivative of furan, containing both aldehyde and ether (methoxymethyl) functional groups. MMF has been detected in the leaves and roots of Chilean ''Jaborosa magellanica'' (Solanaceae). It has a typical odor suggestive of maraschino cherries.Hind, J.D. and Crayton, F.H. (1963) Tobacco flavorants. US 3,095,882 MMF can be made from a wide range of carbohydrate containing feedstocks including sugar, starch and cellulose using a chemical catalytic process and is a potential "carbon-neutr ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hydroxymethylfurfural
Hydroxymethylfurfural (HMF), also 5-(hydroxymethyl)furfural, is an organic compound formed by the dehydration of reducing sugars. It is a white low-melting solid (although commercial samples are often yellow) which is highly soluble in both water and organic solvents. The molecule consists of a furan ring, containing both aldehyde and alcohol functional groups. HMF can form in sugar-containing food, particularly as a result of heating or cooking. Its formation has been the topic of significant study as HMF was regarded as being potentially carcinogenic to humans. However, so far in vivo genotoxicity was negative. No relevance for humans concerning carcinogenic and genotoxic effects can be derived. HMF is classified as a food improvement agent and is primarily being used in the food industry in form of a food additive as a biomarker as well as a flavoring agent for food products. It is also produced industrially on a modest scale as a carbon-neutral feedstock for the production o ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Succinaldehyde
Succinaldehyde or succindialdehyde is an organic compound with the formula (CH2CHO)2. Typical of other dialdehydes, succinaldehyde is highly reactive and is rarely observed as the dialdehyde. Usually, it is handled as the hydrates or methanol-derived acetal. It is a precursor to tropinone. Succinaldehyde can used as a crosslinking agent for proteins, but it is less widely used than the related dialdehyde glutaraldehyde. Preparation and reactions Succinaldehyde is generated by the oxidation of tetrahydrofuran with chlorine followed by hydrolysis of the chlorinated product. It can also be prepared by the hydroformylation of acrolein or the acetals thereof. In aqueous solution, succinaldehyde quickly converts to the cyclic hydrate. In methanol it converts to the cyclic acetal, 2,5-dimethoxyltetrahydrofuran Tetrahydrofuran (THF), or oxolane, is an organic compound with the formula (CH2)4O. The compound is classified as heterocyclic compound, specifically a cyclic ether. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carl Harries
Carl Dietrich Harries (5 August 1866 – 3 November 1923) was a German chemist born in Luckenwalde, Brandenburg, Prussia. He received his doctorate in 1892. In 1900, he married Hertha von Siemens, daughter of the electrical genius Werner von Siemens, and the inventor of one of the earliest ozone generators. In 1904, he moved as full professor to the University of Kiel, where he remained until 1916. During that time he published numerous papers on ozonolysis. His major publication detailing ozonolysis was published in Liebigs Ann. Chem. 1905, 343, 311. Dissatisfied with academic life and having failed to obtain either of two positions at universities, he left academia to become director of research at Siemens and Halske. He died on 3 November 1923 of complications following surgery for cancer. His great-grandfather was the German theologian Heinrich Harries. Accomplishments He investigated polymers and rubber. He showed that rubber consisted of repeating units. He established ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Willy Marckwald
Willy Marckwald (1864, Jakobskirch, Germany – 1942, Rolândia, Brazil) was a German chemist. He was nominated for the Nobel Prize in Chemistry in 1922 by Gustav Tammann and again in 1929 by Niels Bohr, Dirk Coster and George de Hevesy. Biography Marckwald studied at Berlin's Friedrich-Wilhelms-Universität and received there from the First Chemical Institute in 1886 his Promotierung under A. W. Hofmann with a dissertation on organic chemistry entitled ''Beitrag zur Kenntniss der Thialdehyde und Thialdine''. By his research on furans, Marckwald received his Habilitation in a very short time in 1889 under the supervision of A. W. Hofmann at Friedrich-Wilhelms-Universität Berlin. In 1899 Marckwald became one of the department heads at the Second Chemical Institute. He held this Privatdozent-level position until his age-related retirement in 1930. From 1928 to 1931 he was the board chair of the German Chemical Society. In 1890 Marckwald married Margarete Salomon (1871–190 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Heinrich Limpricht
Heinrich Limpricht (21 April 1827 – 13 May 1909) was a German chemist. Limpricht was a pupil of Friedrich Wöhler; he worked on the chemistry of furans and pyrroles, discovering furan in 1870. In 1852 he became lecturer and in 1855 extraordinary professor at the University of Göttingen. In 1860, he became ordinary professor at the Institute for Organic Chemistry at the University of Greifswald. His oldest daughter Marie (1856-1925) married in 1875 to Protestant theologian Julius Wellhausen. Rudolph Fittig and Hans von Pechmann Hans von Pechmann (1 April 1850 – 19 April 1902) was a German chemist, renowned for his discovery of diazomethane in 1894. Pechmann condensation and Pechmann pyrazole synthesis. He also first prepared 1,2-diketones (e.g., diacetyl), acetonedic ... were two of Limpricht's notable pupils. References * * Gerda Schneider: ''Heinrich Limpricht und sein Schülerkreis (1827-1909)''; Diss. Greifswald 1970 Genealogy database entry by Vera V. Ma ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Adolf Von Baeyer
Johann Friedrich Wilhelm Adolf von Baeyer (; 31 October 1835 – 20 August 1917) was a German chemist who synthesised indigo and developed a nomenclature for cyclic compounds (that was subsequently extended and adopted as part of the IUPAC organic nomenclature). He was ennobled in the Kingdom of Bavaria in 1885 and was the 1905 recipient of the Nobel Prize in Chemistry.''Adolf von Baeyer: Winner of the Nobel Prize for Chemistry 1905 '' Armin de Meijere Angewandte Chemie International Edition Volume 44, Issue 48, Pages 7836 – 7840 2005''Abstract/ref> Family and education Baeyer was born in Berlin as the son of the noted geodesist and captain of the Royal Prussian Army Johann Jacob Baeyer and his wife Eugenie Baeyer née Hitzig (1807–1843). Both his parents were Lutherans at the time of his birth and he was raised in the Lutheran religion. His mother was the daughter of Julius Eduard Hitzig and a member of the originally Jewish Itzig family, and had converted to Christianity ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ether
In organic chemistry, ethers are a class of compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. They have the general formula , where R and R′ represent the alkyl or aryl groups. Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. A typical example of the first group is the solvent and anaesthetic diethyl ether, commonly referred to simply as "ether" (). Ethers are common in organic chemistry and even more prevalent in biochemistry, as they are common linkages in carbohydrates and lignin. Structure and bonding Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Auguste André Thomas Cahours
August André Thomas Cahours (1813–1891) was a French chemist and scientist whose contribution to organic chemistry was one of the greatest in history. He discovered, among other things, the processes of synthesis of several chemical molecules, including toluene, xylene, several organo-magnesiums, and derivatives of phosphine and arsine. He was a professor at the École Polytechnique and the École Centrale des Arts et Manufactures. In 1868 he was elected as a member of the Académie des sciences (chemistry section) and in 1880 became a commander of the Légion d'honneur. Sociétés savantes de France Early life Auguste Cahours was born in on 2 October 1813. He was the first of the two children of Rose Adelaide Cartront and ...[...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Oleum
Oleum (Latin ''oleum'', meaning oil), or fuming sulfuric acid, is a term referring to solutions of various compositions of sulfur trioxide in sulfuric acid, or sometimes more specifically to disulfuric acid (also known as pyrosulfuric acid). Oleum is identified by the CAS number 8014-95-7 (EC/List number: 616-954-1 ECHA InfoCard: 100.116.872. Oleums can be described by the formula ''y''SO3·H2O where ''y'' is the total molar mass of sulfur trioxide content. The value of ''y'' can be varied, to include different oleums. They can also be described by the formula H2SO4·''x''SO3 where ''x'' is now defined as the molar free sulfur trioxide content. Oleum is generally assessed according to the free SO3 content by mass. It can also be expressed as a percentage of sulfuric acid strength; for oleum concentrations, that would be over 100%. For example, 10% oleum can also be expressed as H2SO4·''0.13611''SO3, ''1.13611''SO3·H2O or 102.25% sulfuric acid. The conversion between % acid and ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
George Fownes
George Fownes, FRS (14 May 1815 in London – 31 January 1849) was a British chemist. He attended the Palace School in Enfield. He obtained his PhD at Giessen, in Germany. From 1842 he was chemistry professor at the Pharmaceutical Society of Great Britain, and from 1846 at University College, London. He was also secretary of the Chemical Society of London. In 1844, he published a chemistry textbook. In 1842, he had been awarded the Royal Agricultural Society's prize for his essay ''Food of Plants''. In 1844, he received the first Actonian Prize (of 100 guineas) for his essay ''Chemistry as Exemplifies the Wisdom and Beneficence of God''. This work was compared to the ''Bridgewater Treatises'' and Fownes was referred to as "a thorough chemist, a sound philosopher, and an enlightened Christian."Park Benjamin, James Aldrich, Henry Champion Deming, James Mackay (1844). ''The New World: A Weekly Family Journal of Popular Literature, Science, Art and News, Volume 9''. J. Winchester. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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