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Nonacosane
Nonacosane is a straight-chain hydrocarbon with a molecular formula of C29H60, and the structural formula CH3(CH2)27CH3. It has 1,590,507,121 constitutional isomers. Nonacosane occurs naturally and has been reported to be a component of a pheromone of '' Orgyia leucostigma'', and evidence suggests it plays a role in the chemical communication of several insects, including the female ''Anopheles stephensi'' (a mosquito Mosquitoes, the Culicidae, are a Family (biology), family of small Diptera, flies consisting of 3,600 species. The word ''mosquito'' (formed by ''Musca (fly), mosca'' and diminutive ''-ito'') is Spanish and Portuguese for ''little fly''. Mos ...). Nonacosane has been identified within several essential oils. It can also be prepared synthetically. References {{Alkanes Alkanes Insect pheromones ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tetracosane
Tetracosane, also called ''tetrakosane'', is an alkane hydrocarbon with the structural formula H(CH2)24H. As with other alkanes, its name is derived from Greek for the number of carbon atoms, 24, in the molecule. It has 14,490,245 constitutional isomers, and 252,260,276 stereoisomers. ''n''-Tetracosane is found in mineral form, called evenkite, in the Evenki Region on Lower Tunguska River in Siberia and the Bucnik quarry near Konma in eastern Moravia, Czech Republic. Evenkite is found as colourless flakes and is reported to fluoresce yellow-orange. See also * List of alkanes The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. See also * Higher alkane * List of compounds with carbon numbers 50+ ... References External linksNIST Entry Alkanes {{Hydrocarbon-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hentriacontane
Hentriacontane, also called ''untriacontane'', is a solid, long-chain alkane hydrocarbon with the structural formula CH3(CH2)29CH3. It is the main component of paraffin wax. It is found in a variety of plants, including peas (''Pisum sativum''), '' Acacia senegal'', ''Gymnema sylvestre'' and others, and also comprises about 8–9% of beeswax Bee hive wax complex Beeswax (also known as cera alba) is a natural wax produced by honey bees of the genus ''Apis''. The wax is formed into scales by eight wax-producing glands in the abdominal segments of worker bees, which discard it in o .... It has 10,660,307,791 constitutional isomers. References External links Hentriacontaneat Dr. Duke's Phytochemical and Ethnobotanical Databases {{Alkanes Alkanes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Saturated Hydrocarbon
In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. Alkanes have the general chemical formula . The alkanes range in complexity from the simplest case of methane (), where ''n'' = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like hexacontane () or 4-methyl-5-(1-methylethyl) octane, an isomer of dodecane (). The International Union of Pure and Applied Chemistry (IUPAC) defines alkanes as "acyclic branched or unbranched hydrocarbons having the general formula , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms". However, some sources use the term to denote ''any'' saturated hydrocarbon, including those that are either monocyclic (i.e. the cycloalkanes) or polycyclic ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Structural Formula
The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are connected to one another. The chemical bonding within the molecule is also shown, either explicitly or implicitly. Unlike other chemical formula types, which have a limited number of symbols and are capable of only limited descriptive power, structural formulas provide a more complete geometric representation of the molecular structure. For example, many chemical compounds exist in different isomeric forms, which have different enantiomeric structures but the same molecular formula. There are multiple types of ways to draw these structural formulas such as: Lewis structures, condensed formulas, skeletal formulas, Newman projections, Cyclohexane conformations, Haworth projections, and Fischer projections. Several systematic chemical naming formats, as in chemical databases, are used that are equivalent to, an ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Constitutional Isomer
In chemistry, a structural isomer (or constitutional isomer in the IUPAC nomenclature) of a compound is a compound that contains the same number and type of atoms, but with a different connectivity (i.e. arrangement of bonds) between them. The term metamer was formerly used for the same concept. For example, butanol , methyl propyl ether , and diethyl ether have the same molecular formula but are three distinct structural isomers. The concept applies also to polyatomic ions with the same total charge. A classical example is the cyanate ion and the fulminate ion . It is also extended to ionic compounds, so that (for example) ammonium cyanate and urea are considered structural isomers,William F. Bynum, E. Janet Browne, Roy Porter (2014)''Dictionary of the History of Science'' page 218. and so are methylammonium formate and ammonium acetate . Structural isomerism is the most radical type of isomerism. It is opposed to stereoisomerism, in which the atoms and bonding ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pheromone
A pheromone () is a secreted or excreted chemical factor that triggers a social response in members of the same species. Pheromones are chemicals capable of acting like hormones outside the body of the secreting individual, to affect the behavior of the receiving individuals. There are ''alarm signal, alarm pheromones'', ''food trail pheromones'', ''sex pheromones'', and many others that affect behavior or physiology. Pheromones are used by many organisms, from basic unicellular prokaryotes to complex multicellular eukaryotes. Their use among insects has been particularly well documented. In addition, some vertebrates, plants and ciliates communicate by using pheromones. The ecological functions and evolution of pheromones are a major topic of research in the field of chemical ecology. Background The portmanteau word "pheromone" was coined by Peter Karlson and Martin Lüscher in 1959, based on the Greek language, Greek () and (). Pheromones are also sometimes classified as ec ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Orgyia Leucostigma
''Orgyia leucostigma'', the white-marked tussock moth, is a moth in the family Erebidae. The species was first described by James Edward Smith in 1797. The caterpillar is very common especially in late summer in eastern North America, extending as far west as Texas, California, and Alberta. Etymology The genus name ''Orgyia'' is from the ancient Greek word , órgyia - 'outstretched arms'. So named because, when at rest, the moth stretches forward its forelegs like arms. Life cycle Two or more generations occur per year in eastern North America. They overwinter in the egg stage. Eggs Eggs are laid in a single mass over the cocoon of the female, and covered in a froth. Up to 300 eggs are laid at a time. Larvae The larvae are brightly colored, with tufts of hair-like setae. The head is bright red and the body has yellow or white stripes, with a black stripe along the middle of the back. Bright red defensive glands are seen on the hind end of the back. Four white toothbrush-like ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Anopheles Stephensi
''Anopheles stephensi'' is a primary mosquito vector of malaria in urban India and is included in the same subgenus as ''Anopheles gambiae'', the primary malaria vector in Africa. ''A. gambiae'' consists of a complex of morphologically identical species of mosquitoes, along with all other major malaria vectors; however, ''A. stephensi'' has not yet been included in any of these complexes. Nevertheless, two races of ''A. stephensi'' exist based on differences in egg dimensions and the number of ridges on the eggs; ''A. s. stephensi'' ''sensu stricto'', the type form, is a competent malaria vector that is found in urban areas, and ''A. s. mysorensis'', the variety form, exists in rural areas and exhibits considerable zoophilic behaviour, making it a poor malaria vector. However, ''A. s. mysorensis'' is a detrimental vector in Iran.Sinka, M.E., Bangs, M.J., Manguin, S., Chareonviriyaphap, T., Patil, A.P., Temperley, W.H., Gething, P. W., Elyazar, I.R.F., Kabaria, C.W., Harbach, R.E., ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Mosquito
Mosquitoes, the Culicidae, are a Family (biology), family of small Diptera, flies consisting of 3,600 species. The word ''mosquito'' (formed by ''Musca (fly), mosca'' and diminutive ''-ito'') is Spanish and Portuguese for ''little fly''. Mosquitoes have a slender segmented body, one pair of wings, three pairs of long hair-like legs, and specialized, highly elongated, piercing-sucking mouthparts. All mosquitoes drink nectar from flowers; females of some species have in addition adapted to drink blood. The group diversified during the Cretaceous period. Evolutionary biology, Evolutionary biologists view mosquitoes as micropredators, small animals that Parasitism, parasitise larger ones by drinking their blood without immediately killing them. Parasitology, Medical parasitologists view mosquitoes instead as Disease vector, vectors of disease, carrying protozoan parasites or bacterial or virus, viral pathogens from one Host (biology), host to another. The mosquito life cycle cons ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Alkanes
In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. Alkanes have the general chemical formula . The alkanes range in complexity from the simplest case of methane (), where ''n'' = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like hexacontane () or 4-methyl-5-(1-methylethyl) octane, an isomer of dodecane (). The International Union of Pure and Applied Chemistry (IUPAC) defines alkanes as "acyclic branched or unbranched hydrocarbons having the general formula , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms". However, some sources use the term to denote ''any'' saturated hydrocarbon, including those that are either monocyclic (i.e. the cycloalkanes) or polycycl ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
