Not to be confused with Ethylone.
Ethylene
|
|
|
| Names |
| IUPAC name
Ethene
|
| Identifiers |
| CAS number |
74-85-1 Y |
| ChEBI |
CHEBI:18153 Y |
| ChEMBL |
ChEMBL117822 Y |
| ChemSpider |
6085 N |
| EC-number |
200-815-3 |
InChI
-
InChI=1S/C2H4/c1-2/h1-2H2 Y
Key: VGGSQFUCUMXWEO-UHFFFAOYSA-N Y
-
InChI=1/C2H4/c1-2/h1-2H2
Key: VGGSQFUCUMXWEO-UHFFFAOYAE
|
| Jmol-3D images |
Image |
| KEGG |
C06547 Y |
| PubChem |
6325 |
|
|
| UNII |
91GW059KN7 Y |
| Properties |
|
Molecular formula
|
C
2H
4 |
| Molar mass |
28.05 g/mol |
| Appearance |
colorless gas |
| Density |
1.178 kg/m3 at 15 °C, gas[1] |
| Melting point |
−169.2 °C (104.0 K, -272.6 °F) |
| Boiling point |
−103.7 °C (169.5 K, -154.7 °F) |
|
Solubility in water
|
3.5 mg/100 mL (17 °C)[citation needed] ; 2.9 mg/L[2] |
| Solubility in ethanol |
4.22 mg/L[2] |
| Solubility in diethyl ether |
good[2] |
| Acidity (pKa) |
44 |
| Structure |
| Molecular shape |
D2h |
| Dipole moment |
zero |
| Thermochemistry |
|
Std molar
entropy (So298)
|
219.32 J·K−1·mol−1 |
|
Std enthalpy of
formation (ΔfHo298)
|
+52.47 kJ/mol |
| Hazards |
| MSDS |
External MSDS |
| EU classification |
Extremely flammable (F+) |
| NFPA 704 |
|
| Flash point |
−136 °C (−213 °F; 137 K) |
|
Autoignition
temperature
|
542.8 °C (1,009.0 °F; 815.9 K) |
| Related compounds |
|
Related compounds
|
Ethane
Acetylene |
| Supplementary data page |
|
Structure and
properties
|
Refractive index (n),
Dielectric constant (εr), etc. |
|
Thermodynamic
data
|
Phase behaviour
solid–liquid–gas |
|
Spectral data
|
UV, IR, NMR, MS |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
|
| N verify (what is: Y/N?) |
| Infobox references |
|
|
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C
2H
4 or H2C=CH2. It is a colorless flammable gas with a faint "sweet and musky" odor when pure.[3] It is the simplest alkene (a hydrocarbon with carbon-carbon double bonds), and the second simplest unsaturated hydrocarbon after acetylene (C
2H
2).
Ethylene is widely used in chemical industry, and its worldwide production (over 109 million tonnes in 2006) exceeds that of any other organic compound.[4][5] Ethylene is also an important natural plant hormone, used in agriculture to force the ripening of fruits.[6]
Contents
- 1 Structure and properties
- 2 Uses
- 2.1 Polymerization
- 2.2 Oxidation
- 2.3 Halogenation and hydrohalogenation
- 2.4 Alkylation
- 2.5 Oxo reaction
- 2.6 Hydration
- 2.7 Dimerization to n-Butenes
- 2.8 Niche uses
- 3 Production
- 3.1 Industrial Process
- 3.2 Laboratory synthesis
- 4 Ethylene as a plant hormone
- 4.1 History of ethylene in plant biology
- 4.2 Ethylene biosynthesis in plants
- 4.3 Ethylene perception in plants
- 4.4 Environmental and biological triggers of ethylene
- 4.4.1 List of plant responses to ethylene
- 4.4.2 Commercial issues
- 5 Ligand
- 6 History
- 6.1 Nomenclature
- 6.2 Safety
- 7 References
- 8 Further reading
- 9 External links
Structure and properties
Orbital description of bonding between ethylene and a transition metal.
This hydrocarbon has four hydrogen atoms bound to a pair of carbon atoms that are connected by a double bond. All six atoms that comprise ethylene are coplanar. The H-C-H angle is 117.4°, close to the 120° for ideal sp² hybridized carbon. The molecule is also relatively rigid: rotation about the C-C bond is a high energy process that requires breaking the π-bond.
The π-bond in the ethylene molecule is responsible for its useful reactivity. The double bond is a region of high electron density, thus it is susceptible to attack by electrophiles. Many reactions of ethylene are catalyzed by transition metals, which bind transiently to the ethylene using both the π and π* orbitals.
Being a simple molecule, ethylene is spectroscopically simple. Its UV-vis spectrum is still used as a test of theoretical methods.[7]
Uses
Major industrial reactions of ethylene include in order of scale: 1) polymerization, 2) oxidation, 3) halogenation and hydrohalogenation, 4) alkylation, 5) hydration, 6) oligomerization, and 7) hydroformylation. In the United States and Europe, approximately 90% of ethylene is used to produce ethylene oxide, ethylene dichloride, ethylbenzene and polyethylene.[8]
Main industrial uses of ethylene. Clockwise from the upper right: its conversions to ethylene oxide, precursor to ethylene glycol; to ethylbenzene, precursor to styrene; to various kinds of polyethylene; to ethylene dichloride, precursor to vinyl chloride.
Polymerization
See also: Ziegler-Natta catalyst and Polyethylene
Polyethylene consumes more than half of world ethylene supply. Polyethylene, also called polythene, is the world's most widely used plastic, being primarily used to make films used in packaging, carrier bags and trash liners. Linear alpha-olefins, produced by oligomerization (formation of short polymers) are used as precursors, detergents, plasticisers, synthetic lubricants, additives, and also as co-monomers in the production of polyethylenes.[8]
Oxidation
Ethylene is oxidized to produce ethylene oxide, a key raw material in the production of surfactants and detergents by ethoxylation. Ethylene oxide is also hydrolyzed to produce ethylene glycol, widely used as an automotive antifreeze as well as higher molecular weight glycols, glycol ethers and polyethylene terephthalate.
Main article: Wacker process
Ethylene undergoes oxidation by palladium to give acetaldehyde. This conversion remains a major industrial process (10M kg/y).[9] The process proceeds via the initial complexation of ethylene to a Pd(II) center.
Halogenation and hydrohalogenation
Major intermediates from the halogenation and hydrohalogenation of ethylene include ethylene dichloride, ethyl chloride and ethylene dibromide. The addition of chlorine entails "oxychlorination," i.e. chlorine itself is not used. Some products derived from this group are polyvinyl chloride, trichloroethylene, perchloroethylene, methyl chloroform, polyvinylidene chloride and copolymers, and ethyl bromide.[10]
Alkylation
Major chemical intermediates from the alkylation with ethylene is ethylbenzene, precursor to styrene. Styrene is used principally in polystyrene for packaging and insulation, as well as in styrene-butadiene rubber for tires and footwear. On a smaller scale, ethyltoluene, ethylanilines, 1,4-hexadiene, and aluminium alkyls. Products of these intermediates include polystyrene, unsaturated polyesters and ethylene-propylene terpolymers.[10]
Oxo reaction
The hydroformylation (oxo reaction) of ethylene results in propionaldehyde, a precursor to propionic acid and n-propyl alcohol.[10]
Hydration
Ethylene has long represented the major nonfermentative precursor to ethanol. The original method entailed its conversion to diethyl sulfate, followed by hydrolysis. The main method practiced since the mid-1990s is the direct hydration of ethylene catalyzed by solid acid catalysts:[11]
- C2H4 + H2O → CH3CH2OH
Dimerization to n-Butenes
Ethylene can be dimerized to n-butenes using processes licensed by Lummus or IFP. The Lummus process produces mixed n-butenes (primarily 2-butenes) while the IFP process produces 1-butene.
Niche uses
An example of a niche use is as an anesthetic agent (in an 85% ethylene/15% oxygen ratio).[12] It can also be used to hasten fruit ripening, as well as a welding gas.[8][13]
Production
Global ethylene production was 107 million tonnes in 2005,[4] 109 million tonnes in 2006,[14] 138 million tonnes in 2010 and 141 million tonnes in 2011.[15] By 2013 ethylene was produced by at least 117 companies in 32 countries. To meet the ever increasing demand for ethylene, sharp increases in production facilities are added globally, particularly in the Mideast and in China.[16]
Industrial Process
Ethylene is produced in the petrochemical industry by steam cracking. In this process, gaseous or light liquid hydrocarbons are heated to 750–950 °C, inducing numerous free radical reactions followed by immediate quench to stop these reactions. This process converts large hydrocarbons into smaller ones and introduces unsaturation. Ethylene is separated from the resulting complex mixture by repeated compression and distillation. In a related process used in oil refineries, high molecular weight hydrocarbons are cracked over zeolite catalysts. Heavier feedstocks, such as naphtha and gas oils require at least two "quench towers" downstream of the cracking furnaces to recirculate pyrolysis-derived gasoline and process water. When cracking a mixture of ethane and propane, only one water quench tower is required.[10]
The areas of an ethylene plant are:
- steam cracking furnaces:
- primary and secondary heat recovery with quench;
- a dilution steam recycle system between the furnaces and the quench system;
- primary compression of the cracked gas (3 stages of compression);
- hydrogen sulfide and carbon dioxide removal (acid gas removal);
- secondary compression (1 or 2 stages);
- drying of the cracked gas;
- cryogenic treatment;
- all of the cold cracked gas stream goes to the demethanizer tower. The overhead stream from the demethanizer tower consists of all the hydrogen and methane that was in the cracked gas stream. Cryogenically (−250 °F (−157 °C)) treating this overhead stream separates hydrogen from methane. Methane recovery is critical to the economical operation of an ethylene plant.
- the bottom stream from the demethanizer tower goes to the deethanizer tower. The overhead stream from the deethanizer tower consists of all the C
2,'s that were in the cracked gas stream. The C
2 stream contains acetylene, which is explosive above 200 kPa (29 psi).[17] If the partial pressure of acetylene is expected to exceed these values, the C
2 stream is partially hydrogenated. The C
2's then proceed to a C
2 splitter. The product ethylene is taken from the overhead of the tower and the ethane coming from the bottom of the splitter is recycled to the furnaces to be cracked again;
- the bottom stream from the de-ethanizer tower goes to the depropanizer tower. The overhead stream from the depropanizer tower consists of all the C
3's that were in the cracked gas stream. Before feeding the C
3's to the C
3 splitter, the stream is hydrogenated to convert the methylacetylene and propadiene (allene) mix. This stream is then sent to the C
3 splitter. The overhead stream from the C
3 splitter is product propylene and the bottom stream is propane which is sent back to the furnaces for cracking or used as fuel.
- The bottom stream from the depropanizer tower is fed to the debutanizer tower. The overhead stream from the debutanizer is all of the C
4's that were in the cracked gas stream. The bottom stream from the debutanizer (light pyrolysis gasoline) consists of everything in the cracked gas stream that is C
5 or heavier.[10]
Since ethylene production is energy intensive, much effort has been dedicated to recovering heat from the gas leaving the furnaces. Most of the energy recovered from the cracked gas is used to make high pressure (1200 psig) steam. This steam is in turn used to drive the turbines for compressing cracked gas, the propylene refrigeration compressor, and the ethylene refrigeration compressor. An ethylene plant, once running, does not need to import steam to drive its steam turbines. A typical world scale ethylene plant (about 1.5 billion pounds of ethylene per year) uses a 45,000 horsepower (34,000 kW) cracked gas compressor, a 30,000 hp (22,000 kW) propylene compressor, and a 15,000 hp (11,000 kW) ethylene compressor.
Laboratory synthesis
Although of great value industrially, ethylene is rarely used in the laboratory and is ordinarily purchased.[18] It can be produced via dehydration of ethanol with sulfuric acid or in the gas phase with aluminium oxide.[19]
Ethylene as a plant hormone
An ethylene signal transduction pathway. Ethylene permeates the membrane and binds to a receptor on the endoplasmic reticulum. The receptor releases the repressed EIN2. This then activates a signal transduction pathway which activates a regulatory genes that eventually trigger an Ethylene response. The activated DNA is transcribed into mRNA which is then translated into a functional enzyme that is used for ethylene biosynthesis.
Ethylene serves as a hormone in plants.[20] It acts at trace levels throughout the life of the plant by stimulating or regulating the ripening of fruit, the opening of flowers, and the abscission (or shedding) of leaves. Commercial ripening rooms use "catalytic generators" to make ethylene gas from a liquid supply of ethanol. Typically, a gassing level of 500 to 2,000 ppm is used, for 24 to 48 hours. Care must be taken to control carbon dioxide levels in ripening rooms when gassing, as high temperature ripening (20 °C; 68 °F)[citation needed] has been seen to produce CO2 levels of 10% in 24 hours.[21]
History of ethylene in plant biology
Ethylene has been used since the ancient Egyptians, who would gash figs in order to stimulate ripening (wounding stimulates ethylene production by plant tissues). The ancient Chinese would burn incense in closed rooms to enhance the ripening of pears. In 1864, it was discovered that gas leaks from street lights led to stunting of growth, twisting of plants, and abnormal thickening of stems.[20] In 1901, a Russian scientist named Dimitry Neljubow showed that the active component was ethylene.[22] Sarah Doubt discovered that ethylene stimulated abscission in 1917.[23] It wasn't until 1934 that Gane reported that plants synthesize ethylene.[24] In 1935, Crocker proposed that ethylene was the plant hormone responsible for fruit ripening as well as senescence of vegetative tissues.[25]
Ethylene biosynthesis in plants
Ethylene is produced from essentially all parts of higher plants, including leaves, stems, roots, flowers, fruits, tubers, and seeds. Ethylene production is regulated by a variety of developmental and environmental factors. During the life of the plant, ethylene production is induced during certain stages of growth such as germination, ripening of fruits, abscission of leaves, and senescence of flowers. Ethylene production can also be induced by a variety of external aspects such as mechanical wounding, environmental stresses, and certain chemicals including auxin and other regulators.[26]
Ethylene is biosynthesized from the amino acid methionine to S-adenosyl-L-methionine (SAM, also called Adomet) by the enzyme Met Adenosyltransferase. SAM is then converted to 1-aminocyclopropane-1-carboxylic acid (ACC) by the enzyme ACC synthase (ACS). The activity of ACS determines the rate of ethylene production, therefore regulation of this enzyme is key for the ethylene biosynthesis. The final step requires oxygen and involves the action of the enzyme ACC-oxidase (ACO), formerly known as the ethylene forming enzyme (EFE). Ethylene biosynthesis can be induced by endogenous or exogenous ethylene. ACC synthesis increases with high levels of auxins, especially indole acetic acid (IAA) and cytokinins.
Ethylene perception in plants
Ethylene is perceived by a family of five transmembrane protein dimers such as the ETR1 protein in Arabidopsis. The gene encoding an ethylene receptor[which?] has been cloned in Arabidopsis thaliana and then in tomato.[citation needed] Ethylene receptors are encoded by multiple genes in the Arabidopsis and tomato genomes. Mutations in any of the gene family, which comprises five receptors in Arabidopsis and at least six in tomato, can lead to insensitivity to ethylene.[27] DNA sequences for ethylene receptors have also been identified in many other plant species and an ethylene binding protein has even been identified in Cyanobacteria.[20]
Environmental and biological triggers of ethylene
Environmental cues such as flooding, drought, chilling, wounding, and pathogen attack can induce ethylene formation in plants. In flooding, roots suffer from lack of oxygen, or anoxia, which leads to the synthesis of 1-aminocyclopropane-1-carboxylic acid (ACC). ACC is transported upwards in the plant and then oxidized in leaves. The ethylene produced causes nastic movements (epinasty) of the leaves, perhaps helping the plant to lose water.[28]
List of plant responses to ethylene
- Seedling triple response, thickening and shortening of hypocotyl with pronounced apical hook.
- In pollination, when the pollen reaches the stigma, the precursor of the ethene, ACC, is secreted to the petal, the ACC releases ethylene with ACC oxidase.
- Stimulates leaf and flower senescence
- Stimulates senescence of mature xylem cells in preparation for plant use
- Induces leaf abscission
- Induces seed germination
- Induces root hair growth — increasing the efficiency of water and mineral absorption
- Induces the growth of adventitious roots during flooding
- Stimulates epinasty — leaf petiole grows out, leaf hangs down and curls into itself
- Stimulates fruit ripening
- Induces a climacteric rise in respiration in some fruit which causes a release of additional ethylene.
- Affects gravitropism
- Stimulates nutational bending
- Inhibits stem growth and stimulates stem and cell broadening and lateral branch growth outside of seedling stage (see Hyponastic response)
- Interference with auxin transport (with high auxin concentrations)
- Inhibits shoot growth and stomatal closing except in some water plants or habitually flooded ones such as some rice varieties, where the opposite occurs (conserving CO
2 and O
2)
- Induces flowering in pineapples
- Inhibits short day induced flower initiation in Pharbitus nil[29] and Chrysanthemum morifolium[30]
Commercial issues
Ethene shortens the shelf life of many fruits by hastening fruit ripening and floral senescence. Ethene will shorten the shelf life of cut flowers and potted plants by accelerating floral senescence and floral abscission. Flowers and plants which are subjected to stress during shipping, handling, or storage produce ethene causing a significant reduction in floral display. Flowers affected by ethene include carnation, geranium, petunia, rose, and many others.[31]
Ethene can cause significant economic losses for florists, markets, suppliers, and growers. Researchers have developed several ways to inhibit ethene, including inhibiting ethene synthesis and inhibiting ethene perception. Aminoethoxyvinylglycine (AVG), Aminooxyacetic acid (AOA), and silver salts are ethylene inhibitors.[32][33] Inhibiting ethene synthesis is less effective for reducing post-harvest losses since ethene from other sources can still have an effect. By inhibiting ethene perception, fruits, plants and flowers don't respond to ethene produced endogenously or from exogenous sources. Inhibitors of ethene perception include compounds that have a similar shape to ethene, but do not elicit the ethene response. One example of an ethene perception inhibitor is 1-methylcyclopropene (1-MCP).
Commercial growers of bromeliads, including pineapple plants, use ethene to induce flowering. Plants can be induced to flower either by treatment with the gas in a chamber, or by placing a banana peel next to the plant in an enclosed area.
Chrysanthemum flowering is delayed by ethene gas[34] and growers have found that carbon dioxide 'burners' and the exhaust fumes from inefficient glasshouse heaters can raise the ethene concentration to 0.05 vpm causing delay in flowering of commercial crops.
Ligand
Ethylene is a ligand in organometallic chemistry. One of the first organometallic compounds, Zeise's salt is a complex of ethylene. Useful reagents containing ethylene include Pt(PPh3)2(C2H4) and Rh2Cl2(C2H4)4. The Rh-catalysed hydroformylation of ethylene is conducted on industrial scale to provide propionaldehyde.
History
Many geologists and scholars believe that the famous Greek Oracle at Delphi (the Pythia) went into her trance-like state as an effect of ethylene rising from ground faults.[35]
Ethylene appears to have been discovered by Johann Joachim Becher, who obtained it by heating ethanol with sulfuric acid;[36] he mentioned the gas in his Physica Subterranea (1669).[37] Joseph Priestley also mentions the gas in his Experiments and observations relating to the various branches of natural philosophy: with a continuation of the observations on air (1779), where he reports that Jan Ingenhousz saw ethylene synthesized in the same way by a Mr. Enée in Amsterdam in 1777 and that Ingenhousz subsequently produced the gas himself.[38] The properties of ethylene were studied in 1795 by four Dutch chemists, Johann Rudolph Deimann, Adrien Paets van Troostwyck, Anthoni Lauwerenburgh and Nicolas Bondt, who found that it differed from hydrogen gas and that it contained both carbon and hydrogen.[39] This group also discovered that ethylene could be combined with chlorine to produce the oil of the Dutch chemists, 1,2-dichloroethane; this discovery gave ethylene the name used for it at that time, olefiant gas (oil-making gas.)[40]
In the mid-19th century, the suffix -ene (an Ancient Greek root added to the end of female names meaning "daughter of") was widely used to refer to a molecule or part thereof that contained one fewer hydrogen atoms than the molecule being modified. Thus, ethylene (C
2H
4) was the "daughter of ethyl" (C
2H
5). The name ethylene was used in this sense as early as 1852.
In 1866, the German chemist August Wilhelm von Hofmann proposed a system of hydrocarbon nomenclature in which the suffixes -ane, -ene, -ine, -one, and -une were used to denote the hydrocarbons with 0, 2, 4, 6, and 8 fewer hydrogens than their parent alkane.[41] In this system, ethylene became ethene. Hofmann's system eventually became the basis for the Geneva nomenclature approved by the International Congress of Chemists in 1892, which remains at the core of the IUPAC nomenclature. However, by that time, the name ethylene was deeply entrenched, and it remains in wide use today, especially in the chemical industry.
Following experimentation by Luckhardt, Crocker, and Carter at the University of Chicago,[42] ethylene was used as an anesthetic[43][44] It remained in use through the 1940s use even while chloroform was being phased out. Its pungent odor and its explosive nature limit its use today.
Nomenclature
The 1979 IUPAC nomenclature rules made an exception for retaining the non-systematic name ethylene,[45] however, this decision was reversed in the 1993 rules[46] so the IUPAC name is now ethene.
Safety
Like all hydrocarbons, ethylene is an asphyxiant and combustible. It is listed as an IARC class 3 carcinogen.
References
- ^ Record of Ethylene in the GESTIS Substance Database of the IFA, accessed on 25 October 2007
- ^ a b c Нейланд О. Я. Органическая химия: Учебник для хим. спец. вузов.— Москва: Высшая школа, 1990.— с. 128
- ^ Booth, H. S. and Campbell, M. B. (1926) Studies of Anesthetic Ethylene: I. The Odor of Ethylene. Anesthesia and Analgesia, July–August 1929, pages 221-226.
- ^ a b "Production: Growth is the Norm". Chemical and Engineering News (PDF) 84 (28): 59. July 10, 2006. doi:10.1021/cen-v084n034.p059.
- ^ "Propylene Production from Methanol". by Intratec, ISBN 978-0-615-64811-8.
- ^ Wang K, Li H, Ecker J; Li; Ecker (2002). "Ethylene Biosynthesis and Signaling Networks". Plant Cell 14 (Suppl): S131–51. doi:10.1105/tpc.001768 (inactive 2015-01-10). PMC 151252. PMID 12045274.
- ^ "Ethylene:UV/Visible Spectrum". NIST Webbook. Retrieved 2006-09-27.
- ^ a b c "OECD SIDS Initial Assessment Profile — Ethylene" (PDF). inchem.org. Retrieved 2008-05-21.
- ^ Elschenbroich, C.; Salzer, A. (2006). Organometallics : A Concise Introduction (2nd ed.). Weinheim: Wiley-VCH. ISBN 3-527-28165-7.
- ^ a b c d e Kniel, Ludwig; Winter, Olaf; Stork, Karl (1980). Ethylene, keystone to the petrochemical industry. New York: M. Dekker. ISBN 0-8247-6914-7.
- ^ Naim Kosaric, Zdravko Duvnjak, Adalbert Farkas, Hermann Sahm, Stephanie Bringer-Meyer, Otto Goebel and Dieter Mayer in "Ethanol" Ullmann's Encyclopedia of Industrial Chemistry, 2011, Wiley-VCH, Weinheim. doi:10.1002/14356007.a09_587.pub2
- ^ Hugh H. Trout (1927). "Blood Changes Under Ethylene Anæsthesia". Annals of Surgery 86 (2): 260–7. doi:10.1097/00000658-192708000-00013. PMC 1399426. PMID 17865725.
- ^ "Informational Bulletin" 12. California Fresh Market Advisory Board. June 1, 1976.
- ^ Nattrass, L and Higson, A (22 July 2010) NNFCC Renewable Chemicals Factsheet: Ethanol. National Non-Food Crops Centre
- ^ Warren R. True, Oil and Gas Journal, 2012, vol 110, issue 7
- ^ "Market Study: Ethylene (2nd edition), Ceresana, November 2014". ceresana.com. Retrieved 2015-02-03.
- ^ Korzun, Mikołaj (1986). 1000 słów o materiałach wybuchowych i wybuchu. Warszawa: Wydawnictwo Ministerstwa Obrony Narodowej. ISBN 83-11-07044-X. OCLC 69535236.
- ^ Crimmins, M.T.; Kim-Meade, A.S. (2004). "Ethylene". In Paquette, L. Encyclopedia of Reagents for Organic Synthesis. New York: Wiley. doi:10.1002/047084289.
- ^ Cohen, Julius B. (1930). Practical Organic Chemistry (preparation 4). Macmillan.
- ^ a b c Lin, Z.; Zhong, S.; Grierson, D. (2009). "Recent advances in ethylene research". J. Exp. Bot. 60 (12): 3311–36. doi:10.1093/jxb/erp204. PMID 19567479.
- ^ External Link to More on Ethylene Gassing and Carbon Dioxide Control. ne-postharvest.com
- ^ Neljubov D. (1901). "Uber die horizontale Nutation der Stengel von Pisum sativum und einiger anderen Pflanzen". Beih Bot Zentralbl 10: 128–139.
- ^ Doubt, Sarah L. (1917). "The Response of Plants to Illuminating Gas". Botanical Gazette 63 (3): 209–224. doi:10.1086/332006. JSTOR 2469142.
- ^ Gane R. (1934). "Production of ethylene by some fruits". Nature 134 (3400): 1008. Bibcode:1934Natur.134.1008G. doi:10.1038/1341008a0.
- ^ Crocker W, Hitchcock AE, Zimmerman PW. (1935) "Similarities in the effects of ethlyene and the plant auxins". Contrib. Boyce Thompson Inst. 7. 231-48. Auxins Cytokinins IAA Growth substances, Ethylene
- ^ Yang, S. F., and Hoffman N. E. (1984). "Ethylene biosynthesis and its regulation in higher plants". Ann. Rev. Plant Physiol. 35: 155–89. doi:10.1146/annurev.pp.35.060184.001103.
- ^ Bleecker, A. B.; Esch, J. J.; Hall, A. E.; Rodríguez, F. I.; Binder, B. M. (1998). "The ethylene-receptor family from Arabidopsis: Structure and function". Philosophical Transactions of the Royal Society B: Biological Sciences 353 (1374): 1405–12. doi:10.1098/rstb.1998.0295. PMC 1692356. PMID 9800203. edit
- ^ Explaining Epinasty. planthormones.inf
- ^ Wilmowicz E, Kesy J, Kopcewicz J; Kesy; Kopcewicz (December 2008). "Ethylene and ABA interactions in the regulation of flower induction in Pharbitis nil". J. Plant Physiol. 165 (18): 1917–28. doi:10.1016/j.jplph.2008.04.009. PMID 18565620.
- ^ Cockshull KE, Horridge JS (1978). "2-Chloroethylphosphonic Acid and Flower Initiation by Chrysanthemum morifolium Ramat. In Short Days and in Long Days". Journal of Horticultural Science & Biotechnology 53 (2): 85–90.
- ^ Van Doorn, W. G. (2002). "Effect of ethylene on flower abscission: a survey". Annals of Botany 89 (6): 689–693. doi:10.1093/aob/mcf124. PMC 4233834. PMID 12102524.
- ^ Cassells, A. C.; Peter B. Gahan (2006). Dictionary of plant tissue culture. Haworth Press. p. 77. ISBN 978-1-56022-919-3.
- ^ Constabel, Friedrich; Jerry P. Shyluk (1994). "1: Initiation, Nutrition, and Maintenance of Plant Cell and Tissue Cultures". Plant Cell and Tissue Culture. Springer. p. 5. ISBN 0-7923-2493-5.
- ^ van Berkel, N. (1987). "Injurious effects of low ethylene concentrations on Chrysanthemum morifolium Ramat". Acta Hort. (ISHS) 197: 43–52.
- ^ John Roach (2001-08-14). "Delphic Oracle's Lips May Have Been Loosened by Gas Vapors". National Geographic. Retrieved March 8, 2007.
- ^ Roscoe, Henry Enfield; Schorlemmer, Carl (1878). A treatise on chemistry 1. D. Appleton. p. 611.
- ^ Brown, James Campbell (July 2006). A History of Chemistry: From the Earliest Times Till the Present Day. Kessinger. p. 225. ISBN 978-1-4286-3831-0.
- ^ Appendix, §VIII, pp. 474 ff., Experiments and observations relating to the various branches of natural philosophy: with a continuation of the observations on air, Joseph Priestley, London: printed for J. Johnson, 1779, vol. 1.
- ^ Roscoe & Schorlemmer 1878, p. 612
- ^ Roscoe & Schorlemmer 1878, p. 613
Gregory, William (1857). Handbook of organic chemistry (4th American ed.). A.S. Barnes & Co. p. 157.
- ^ A. W. Hofmann, LL.D., F.R.S. "Hofmann's Proposal for Systematic Nomenclature of the Hydrocarbons". www.chem.yale.edu. Retrieved 2007-01-06.
- ^ Luckhardt, Arno; Carter, J. B. (1 Dec 1923). "Ethylene as a gas anesthetic". Current Researches in Anesthesisa & Analgeisa 2 (6): 221–229. Retrieved 11 January 2015.
- ^ Johnstone, George A. Johnstone (1 Aug 1927). "Advantages of Ethylene-Oxygen as an anesthetic". California and Western Medicine (ACS) 27 (2): 216–218. PMC 1655579. PMID 18740435.
- ^ Zimmermann, Heinz; Walz, Roland (2008). "Ethylene". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_045.pub3.
- ^ IUPAC nomenclature rule A-3.1 (1979)
- ^ Footnote to IUPAC nomenclature rule R-9.1, table 19(b)
Further reading
- Chang C, Stadler R; Stadler (July 2001). "Ethylene hormone receptor action in Arabidopsis". BioEssays 23 (7): 619–27. doi:10.1002/bies.1087. PMID 11462215.
- Millenaar FF, van Zanten M, Cox MC, Pierik R, Voesenek LA, Peeters AJ; Van Zanten; Cox; Pierik; Voesenek; Peeters (2009). "Differential petiole growth in Arabidopsis thaliana: photocontrol and hormonal regulation". New Phytol. 184 (1): 141–52. doi:10.1111/j.1469-8137.2009.02921.x. PMID 19558423.
- Schaller, George E (2012). "Ethylene and the regulation of plant development". BMC Biology (20 February 2012) 10 (9): 9. doi:10.1186/1741-7007-10-9. Retrieved February 20, 2012.
External links
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Wikimedia Commons has media related to Ethylene. |
- International Chemical Safety Card 0475
- European Chemicals Bureau Datasheet
- Speculations Towards a General Plant Hormone Theory
- MSDS
|
Alkenes
|
|
- Ethene ( C
2H
4 )
- Propene ( C
3H
6 )
- Butene ( C
4H
8 )
- Pentene ( C
5H
10 )
- Hexene ( C
6H
12 )
- Heptene ( C
7H
14 )
- Octene ( C
8H
16 )
- Nonene ( C
9H
18 )
- Decene ( C
10H
20 )
|
|
|
Functional groups
|
|
- Acetyl
- Acetoxy
- Acryloyl
- Acyl
- Alcohol
- Aldehyde
- Alkane
- Alkene
- Alkyne
- Alkoxy group
- Amide
- Amine
- Azo compound
- Benzene derivative
- Carbene
- Carbonyl
- Carboxylic acid
- Cyanate
- Disulfide
- Dioxirane
- Ester
- Ether
- Epoxide
- Haloalkane
- Hydrazone
- Hydroxyl
- Imide
- Imine
- Isocyanate
- Isonitrile
- Isothiocyanate
- Ketone
- Methyl
- Methylene bridge
- Methylene group
- Methine
- Nitrile
- Nitrene
- Nitro compound
- Nitroso compound
- Organophosphorus
- Oxime
- Peroxide
- Phosphonous and Phosphonic acid
- Pyridine derivative
- Selenol
- Selenonic acid
- Sulfone
- Sulfonic acid
- Sulfoxide
- Tellurol
- Thial
- Thiocyanate
- Thioester
- Thioether
- Thioketone
- Thiol
- Urea
|
|
|
See also Chemical classification
|
|
|
Molecules detected in outer space
|
|
| Molecules |
|
|
Deuterated
molecules |
- Ammonia
- Ammonium ion
- Formaldehyde
- Formyl radical
- Heavy water
- Hydrogen cyanide
- Hydrogen deuteride
- Hydrogen isocyanide
- Methylacetylene
- N2D+
- Trihydrogen cation
|
|
| Unconfirmed |
- Anthracene
- Dihydroxyacetone
- Ethyl methyl ether
- Glycine
- Graphene
- H2NCO+
- Linear C5
- Naphthalene cation
- Phosphine
- Pyrene
- Silylidine
|
|
| Related |
- Abiogenesis
- Astrobiology
- Astrochemistry
- Atomic and molecular astrophysics
- Chemical formula
- Circumstellar envelope
- Cosmic dust
- Cosmic ray
- Cosmochemistry
- Diffuse interstellar band
- Extraterrestrial life
- Extraterrestrial liquid water
- Forbidden mechanism
- Helium hydride ion
- Homochirality
- Intergalactic dust
- Interplanetary medium
- Interstellar medium
- Iron–sulfur world theory
- Kerogen
- Life
- Organic compound
- Outer space
- PAH world hypothesis
- Panspermia
- Polycyclic aromatic hydrocarbon (PAH)
- RNA world hypothesis
- Spectroscopy
- Tholin
|
|
- Book:Chemistry
- Category:Astrochemistry
- Category:Molecules
- Portal:Astrobiology
- Portal:Chemistry
|
|
|
General anesthetics (N01A)
|
|
| Inhalational |
- Chloroethane (ethyl chloride)‡
- Chloroform‡
- Cyclopropane‡
- Desflurane
- Diethyl ether‡
- Enflurane
- Ethylene‡
- Fluroxene‡
- Halothane#
- Isoflurane
- Methoxyflurane
- Methoxypropane‡
- Nitrous oxide#
- Sevoflurane
- Trichloroethylene‡
- Vinyl ether‡
- Xenon
|
|
| Injection |
|
Barbiturates
|
- Hexobarbital
- Methohexital
- Narcobarbital
- Thiopental#
- Thiotetrabarbital
|
|
|
Opioids
|
- Alfentanil
- Anileridine‡
- Fentanyl
- Phenoperidine
- Remifentanil
- Sufentanil
|
|
|
Arylcyclohexylamines
|
- Esketamine
- Ketamine#
- Phencyclidine‡
- Tiletamine
|
|
|
Others
|
- Alfadolone
- Alfaxalone
- Etomidate
- Fospropofol
- Hydroxydione
- GHB
- Metomidate
- Midazolam
- Propanidid‡
- Propofol
|
|
|
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
|
|
Index of the central nervous system
|
|
| Description |
- Anatomy
- meninges
- cortex
- association fibers
- commissural fibers
- lateral ventricles
- basal ganglia
- diencephalon
- mesencephalon
- pons
- cerebellum
- medulla
- spinal cord
- Physiology
- Development
|
|
| Disease |
- Meningitis
- Demyelinating diseases
- Seizures and epilepsy
- Headache
- Stroke
- Sleep
- Congenital
- Injury
- Neoplasms and cancer
- Other
- Symptoms and signs
- head and neck
- eponymous
- lesions
|
|
| Treatment |
- Procedures
- Drugs
- general anesthetics
- analgesics
- addiction
- epilepsy
- cholinergics
- migraine
- Parkinson's
- vertigo
- other
|
|
|
|
Plant hormones
|
|
- Abscisic acid
- Auxins
- Cytokinins
- Ethylene
- Gibberellins
|
|
- Brassinosteroids
- Florigen
- Jasmonates
- Karrikins
- Plant peptide hormones
- Polyamine
- Salicylic acid
- Strigolactones
|
|
|
GABAAR PAMs
|
|
| Alcohols |
- Brometone
- Butanol
- Chloralodol
- Chlorobutanol (cloretone)
- Ethanol (drinking alcohol)
- Ethchlorvynol
- Isobutanol
- Isopropanol
- Menthol
- Methanol
- Methylpentynol
- Pentanol
- Petrichloral
- Propanol
- tert-Butanol (2M2P)
- tert-Pentanol (2M2B)
- Tribromoethanol
- Trichloroethanol
- Triclofos
- Trifluoroethanol
|
|
| Barbiturates |
- (-)-DMBB
- Allobarbital
- Alphenal
- Amobarbital
- Aprobarbital
- Barbexaclone
- Barbital
- Benzobarbital
- Benzylbutylbarbiturate
- Brallobarbital
- Brophebarbital
- Butabarbital/Secbutabarbital
- Butalbital
- Buthalital
- Butobarbital
- Butallylonal
- Carbubarb
- CP-1414S
- Crotylbarbital
- Cyclobarbital
- Cyclopentobarbital
- Difebarbamate
- Enallylpropymal
- Ethallobarbital
- Eterobarb
- Febarbamate
- Heptabarb
- Heptobarbital
- Hexethal
- Hexobarbital
- Metharbital
- Methitural
- Methohexital
- Methylphenobarbital
- Motrazepam
- Narcobarbital
- Nealbarbital
- Pentobarbital
- Phenallymal
- Phenobarbital
- Phetharbital
- Primidone
- Probarbital
- Propallylonal
- Propylbarbital
- Proxibarbital
- Reposal
- Secobarbital
- Sigmodal
- Spirobarbital
- Talbutal
- Tetrabamate
- Tetrabarbital
- Thialbarbital
- Thiamylal
- Thiobarbital
- Thiobutabarbital
- Thiopental
- Thiotetrabarbital
- Valofane
- Vinbarbital
- Vinylbital
|
|
| Benzodiazepines |
- 2-Oxoquazepam
- 3-Hydroxyphenazepam
- Adinazolam
- Alprazolam
- Arfendazam
- Avizafone
- Bentazepam
- Bretazenil
- Bromazepam
- Brotizolam
- Camazepam
- Carburazepam
- Chlordiazepoxide
- Ciclotizolam
- Cinazepam
- Cinolazepam
- Clazolam
- Climazolam
- Clobazam
- Clonazepam
- Clorazepate
- Clotiazepam
- Cloxazolam
- Cyprazepam
- Delorazepam
- Demoxepam
- Diazepam
- Diclazepam
- Doxefazepam
- Elfazepam
- Estazolam
- Ethyl carfluzepate
- Ethyl dirazepate
- Ethyl loflazepate
- Etizolam
- EVT-201
- FG-8205
- Fletazepam
- Flubromazepam
- Flubromazolam
- Fludiazepam
- Flunitrazepam
- Flurazepam
- Flutazolam
- Flutemazepam
- Flutoprazepam
- Fosazepam
- Gidazepam
- Halazepam
- Haloxazolam
- Iclazepam
- Imidazenil
- Ketazolam
- Lofendazam
- Lopirazepam
- Loprazolam
- Lorazepam
- Lormetazepam
- Meclonazepam
- Medazepam
- Menitrazepam
- Metaclazepam
- Mexazolam
- Midazolam
- N-Desalkylflurazepam
- Nimetazepam
- Nitrazepam
- Nitrazepate
- Nordazepam
- Nortetrazepam
- Oxazepam
- Oxazolam
- Phenazepam
- Pinazepam
- Pivoxazepam
- Prazepam
- Premazepam
- Proflazepam
- Pyrazolam
- QH-II-66
- Quazepam
- Reclazepam
- Remimazolam
- Rilmazafone
- Ripazepam
- Ro48-6791
- Ro48-8684
- SH-053-R-CH3-2′F
- Sulazepam
- Temazepam
- Tetrazepam
- Tolufazepam
- Triazolam
- Triflubazam
- Triflunordazepam (Ro5-2904)
- Tuclazepam
- Uldazepam
- Zapizolam
- Zolazepam
- Zomebazam
|
|
| Carbamates |
- Carisbamate
- Carisoprodol
- Clocental
- Cyclarbamate
- Difebarbamate
- Emylcamate
- Ethinamate
- Febarbamate
- Felbamate
- Hexapropymate
- Lorbamate
- Mebutamate
- Meprobamate
- Methocarbamol
- Nisobamate
- Pentabamate
- Phenprobamate
- Procymate
- Styramate
- Tetrabamate
- Tybamate
|
|
| Flavonoids |
- 6-Methylapigenin
- Ampelopsin (dihydromyricetin)
- Apigenin
- Baicalein
- Baicalin
- Catechin
- EGC
- EGCG
- Hispidulin
- Linarin
- Luteolin
- Rc-OMe
- Skullcap constituents (e.g., baicalin)
- Wogonin
|
|
| Imidazoles |
- Etomidate
- Metomidate
- Propoxate
|
|
| Neuroactive steroids |
- Acebrochol
- Allopregnanolone
- Alfadolone
- Alfaxalone
- 3α-Androstanediol
- Androsterone
- Cholesterol
- DHDOC
- 5α-DHP
- Etiocholanolone
- Ganaxolone
- Hydroxydione
- Minaxolone
- Org 20599
- Org 21465
- Pregnanolone (eltanolone)
- Renanolone
- THDOC
|
|
| Nonbenzodiazepines |
- β-Carbolines: Abecarnil
- Gedocarnil
- Harmane
- SL-651,498
- ZK-93423; Cyclopyrrolones: Eszopiclone
- Pagoclone
- Pazinaclone
- Suproclone
- Suriclone
- Zopiclone; Imidazopyridines: Alpidem
- DS-1
- Necopidem
- Saripidem
- Zolpidem; Pyrazolopyrimidines: Divaplon
- Fasiplon
- Indiplon
- Lorediplon
- Ocinaplon
- Panadiplon
- Taniplon
- Zaleplon; Others: Adipiplon
- CGS-8216
- CGS-9896
- CGS-13767
- CGS-20625
- CL-218,872
- CP-615,003
- CTP-354
- ELB-139
- GBLD-345
- JM-1232
- L-838,417
- Lirequinil (Ro41-3696)
- NS-2664
- NS-2710
- NS-11394
- Pipequaline
- ROD-188
- RWJ-51204
- SB-205,384
- SX-3228
- TP-003
- TPA-023
- TP-13
- U-89843A
- U-90042
- Y-23684
|
|
| Phenols |
- Fospropofol
- Propofol
- Thymol
|
|
| Piperidinediones |
- Glutethimide
- Methyprylon
- Piperidione
- Pyrithyldione
|
|
| Pyrazolopyridines |
- Cartazolate
- Etazolate
- ICI-190,622
- Tracazolate
|
|
| Quinazolinones |
- Afloqualone
- Cloroqualone
- Diproqualone
- Etaqualone
- Mebroqualone
- Mecloqualone
- Methaqualone
- Methylmethaqualone
- Nitromethaqualone
- SL-164
|
|
| Volatiles/gases |
- Acetone
- Acetophenone
- Acetylglycinamide chloral hydrate
- Aliflurane
- Benzene
- Butane
- Butylene
- Centalun
- Chloral
- Chloral hydrate
- Chloroform
- Cryofluorane
- Desflurane
- Dichloralphenazone
- Dichloromethane
- Diethyl ether
- Enflurane
- Ethyl chloride
- Ethylene
- Fluroxene
- Gasoline
- Halopropane
- Halothane
- Isoflurane
- Kerosine
- Methoxyflurane
- Methoxypropane
- Nitric oxide
- Nitrogen
- Nitrous oxide
- Norflurane
- Paraldehyde
- Propane
- Propylene
- Roflurane
- Sevoflurane
- Synthane
- Teflurane
- Toluene
- Trichloroethane (methyl chloroform)
- Trichloroethylene
- Vinyl ether
|
|
| Others/unsorted |
- 3-Hydroxybutanal
- α-EMTBL
- AA-29504
- Avermectins (e.g., ivermectin)
- Bromide compounds (e.g., lithium bromide, potassium bromide, sodium bromide)
- Carbamazepine
- Chloralose
- Chlormezanone
- Clomethiazole
- DEABL
- Dihydroergolines (e.g., dihydroergocryptine, dihydroergosine, dihydroergotamine, ergoloid (dihydroergotoxine))
- DS2
- Efavirenz
- Etazepine
- Etifoxine
- Fenamates (e.g., flufenamic acid, mefenamic acid, niflumic acid, tolfenamic acid)
- Fluoxetine
- Flupirtine
- Hopantenic acid
- Kava constituents (e.g., dihydrokavain, dihydromethysticin, kavain, methysticin, yangonin)
- Lanthanum
- Lignans (e.g., 4-O-methylhonokiol, honokiol, magnolol, obovatol)
- Loreclezole
- Menthyl isovalerate (validolum)
- Monastrol
- Niacin
- Nicotinamide (niacinamide)
- Norfluoxetine
- Org 25,435
- Phenytoin
- Propanidid
- Retigabine (ezogabine)
- Safranal
- Stiripentol
- Sulfonylalkanes (e.g., sulfonmethane (sulfonal), tetronal, trional)
- Terpenoids (e.g., borneol)
- Topiramate
- Valerian constituents (e.g., isovaleric acid, valerenic acid, valerenol)
- Unsorted benzodiazepine site PAMs: MRK-409 (MK-0343)
- TCS-1105
- TCS-1205
|
|
|
See also: GABAergics
|
|