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''tert''-Amyl methyl ether (TAME) is an
ether In organic chemistry, ethers are a class of compounds that contain an ether group, a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl). They have the general formula , where R and R� ...
used as a fuel oxygenate. TAME derives from C5 distillation fractions of
naphtha Naphtha (, recorded as less common or nonstandard in all dictionaries: ) is a flammable liquid hydrocarbon mixture. Generally, it is a fraction of crude oil, but it can also be produced from natural-gas condensates, petroleum distillates, and ...
. It has an ethereous
odor An odor (American English) or odour ( Commonwealth English; see spelling differences) is a smell or a scent caused by one or more volatilized chemical compounds generally found in low concentrations that humans and many animals can perceive ...
. Unlike most ethers, it does not require a stabilizer as it does not form
peroxides In chemistry, peroxides are a group of compounds with the structure , where the R's represent a radical (a portion of a complete molecule; not necessarily a free radical) and O's are single oxygen atoms. Oxygen atoms are joined to each other and ...
on storage. Other names: * 2-Methoxy-2-methylbutane * Butane, 2-methoxy-2-methyl- * 1,1-Dimethylpropyl methyl ether * Methyl tert-pentyl ether * Methyl tert-Amyl ether * 2-Methyl-2-methoxybutane * Methyl 2-methyl-2-butyl ether * tert-Pentyl methyl ether * Tertiary amyl methyl ether * Methyl 1,1-dimethylpropyl ether * 2-Methoxy-2-methylbutane


Uses

TAME is mostly used as an
oxygenate In the liquid fuel industry, oxygenates are hydrocarbon-derived fuel additives containing at least one oxygen atom to promote complete combustion. Absent oxygenates, fuel combustion is usually incomplete, and the exhaust stream pollutes the air ...
to gasoline. It is added for three reasons: to increase
octane Octane is a hydrocarbon and also an alkane with the chemical formula C8H18, and the condensed structural formula CH3(CH2)6CH3. Octane has many structural isomers that differ by the location of branching in the carbon chain. One of these isomers ...
enhancement, to replace banned
tetraethyl lead Tetraethyllead (commonly styled tetraethyl lead), abbreviated TEL, is an organolead compound with the formula Pb( C2H5)4. It was widely used as a fuel additive for much of the 20th century, first being mixed with gasoline beginning in the 192 ...
, and to raise the
oxygen Oxygen is a chemical element; it has chemical symbol, symbol O and atomic number 8. It is a member of the chalcogen group (periodic table), group in the periodic table, a highly reactivity (chemistry), reactive nonmetal (chemistry), non ...
content in
gasoline Gasoline ( North American English) or petrol ( Commonwealth English) is a petrochemical product characterized as a transparent, yellowish, and flammable liquid normally used as a fuel for spark-ignited internal combustion engines. When for ...
. It is known that TAME in fuel reduces
exhaust Exhaust, exhaustive, or exhaustion may refer to: Law * Exhaustion of intellectual property rights, limits to intellectual property rights in patent and copyright law ** Exhaustion doctrine, in patent law ** Exhaustion doctrine under U.S. law, i ...
emissions of some
volatile organic compounds Volatile organic compounds (VOCs) are organic compounds that have a high vapor pressure at room temperature. They are common and exist in a variety of settings and products, not limited to house mold, upholstered furniture, arts and crafts sup ...
. TAME is also used as a solvent in
organic synthesis Organic synthesis is a branch of chemical synthesis concerned with the construction of organic compounds. Organic compounds are molecules consisting of combinations of covalently-linked hydrogen, carbon, oxygen, and nitrogen atoms. Within the gen ...
as a more environmentally friendly alternative to some of the classic ether solvents. It is characterized by a high boiling point (86°C) and a low freezing point (−80°C), allowing a wide range of reaction temperatures. TAME can be used as a safe reaction medium (e.g.
condensation reaction In organic chemistry, a condensation reaction is a type of chemical reaction in which two molecules are combined to form a single molecule, usually with the loss of a small molecule such as water. If water is lost, the reaction is also known as a ...
s, coupling reactions, such as
Grignard reaction The Grignard reaction () is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent) are added to the carbonyl groups of either an aldehyde or ...
s and
Suzuki reaction The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemi ...
s, as well as metal hydride reductions) and as an extraction solvent to replace
dichloromethane Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula . This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with ...
, aromatics, and other ethers. A series of experiments were carried out in a batch reactor at the temperature range of 313-343 K to study the synthesis of ''tert''-amyl ethyl ether from ethanol (EtOH) and 2-methyl-1-butene (2M1B) catalyzed by the NKC-9 ion-exchange resin. The suitable reaction pressure was obtained by using the method of the Gibbs free energy minimization. The activity coefficients of each component were accurately calculated using the Wilson method, then, the equilibrium constants was obtained. The effect of catalyst size, stirring rate, temperature and EtOH/2M1B molar ratio was investigated at the chosen pressure, respectively. A kinetic model which considered the variation of each component volume was established. The method of nonlinear least square combined with genetic algorithm (NLS-GA) was proposed to estimate the kinetic constant in the forward direction. Results indicated that simulated kinetics results were agreed well with the experimental data.


Toxicity

TAME was evaluated in 4-week rat inhalation studies sponsored by Amoco Corporation. Target vapor concentrations were 0, 500, 2000, or 4000 ppm for 6 h per day, 5 days per week, for 4 weeks. Exposure at 4000 ppm resulted in 25% mortality, apparently as a consequence of severe CNS depression. Body weight gain was decreased in the TAME high dose male rats. Significant effects on functional observational battery (FOB) parameters were only found in the high and mid-dose groups immediately after exposure. All affected FOB parameters were normal by the next day. TAME exposure significantly increased relative liver weights in the high and mid-dose groups. However, no treatment-related histopathologic findings were noted for the compound. Clinical chemistry and hematology findings were minimal with TAME exposure. The results indicate that 500 ppm was a NOAEL for TAME in these studies.


Some other properties

Relative vapor density (air = 1): 3.6 Vapor Pressure 75.2 mHg log Kow = 1.55 at 20 °C Henry's Law constant = 1.32X10-3 atm-cu m/mol at 25 °C Stability / Shelf Life: Stable under recommended storage conditions. Autoignition Temperature: 415 °C Decomposition: When heated to decomposition it emits acrid smoke and irritating vapors. Odor Threshold: 0.02 mHg


Kovats retention index

Standard non-polar 672.5, 674, 673, 669.3, 666 Semi-standard non-polar 678, 655, 668.3 Standard polar 790, 802.9


See also

* Methyl ''tert''-butyl ether * Ethyl ''tert''-butyl ether *
List of gasoline additives Gasoline additives may increase gasoline's octane rating, thus allowing the use of higher compression ratios for greater efficiency and power, or act as corrosion inhibitors or lubricants. Other additives include metal deactivators, oxygenates and ...


References

{{DEFAULTSORT:Amyl Methyl Ether, Tert- Dialkyl ethers Oxygenates Ether solvents Methoxy compounds