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tert-Butyl methyl ether

CAS No.
1634-04-4
Chemical Name:
tert-Butyl methyl ether
Synonyms
MTBE;TBME;METHYL TERT-BUTYL ETHER;MTB;2-Methoxy-2-methylpropane;BOC-ARG(MTR)-OH;T-BUTYL METHYL ETHER;Methyl tert-butyl ether, for residue analysis;METHYL-T-BUTYL ETHER;2-methoxy-2-methyl
CBNumber:
CB2853178
Molecular Formula:
C5H12O
Molecular Weight:
88.15
MDL Number:
MFCD00008812
MOL File:
1634-04-4.mol
MSDS File:
SDS
Last updated:2024-11-13 18:13:23

tert-Butyl methyl ether Properties

Melting point -110 °C
Boiling point 55-56 °C(lit.)
Density 0.7404
vapor density 3.1 (vs air)
vapor pressure 4.05 psi ( 20 °C)
refractive index n20/D 1.369(lit.)
Flash point -27 °F
storage temp. Store at +2°C to +25°C.
solubility 42g/l
form Powder or Needles
color APHA: ≤10
Specific Gravity 0.740
Relative polarity 0.124
Odor Characteristic ethereal odor
Relative density, gas (air=1) 0.74 g/cm3 at 25 °C
Viscosity 0.464mm2/s
explosive limit 1.5-8.5%(V)
Water Solubility 51 g/L (20 ºC)
FreezingPoint -108.6℃
λmax λ: 210 nm Amax: 1.0
λ: 225 nm Amax: 0.50
λ: 250 nm Amax: 0.10
λ: 300-400 nm Amax: 0.005
Merck 14,6032
BRN 1730942
Exposure limits ACGIH: TWA 50 ppm
Dielectric constant 4.5
Stability Stable, but may form explosive peroxides in contact with air. Extremely flammable - note low flash point. Incompatible with strong oxidizing agents.
InChIKey BZLVMXJERCGZMT-UHFFFAOYSA-N
LogP 1.06 at 20℃
CAS DataBase Reference 1634-04-4(CAS DataBase Reference)
EWG's Food Scores 5
FDA UNII 29I4YB3S89
NIST Chemistry Reference Propane, 2-methoxy-2-methyl-(1634-04-4)
IARC 3 (Vol. 73) 1999
EPA Substance Registry System Methyl tert-butyl ether (1634-04-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H315
Precautionary statements  P210-P233-P240-P241-P242-P303+P361+P353
Hazard Codes  Xn,F,Xi,T
Risk Statements  36/37/38-40-38-11-39/23/24/25-23/24/25
Safety Statements  9-16-24-45-36/37-7
RIDADR  UN 2398 3/PG 2
WGK Germany  3
RTECS  KN5250000
3-10
Autoignition Temperature 705 °F
TSCA  Yes
HS Code  2909 19 90
HazardClass  3
PackingGroup  II
Toxicity . LC50 in mice (15 min): 1.6 mmol/liter of atmosphere (Marsh)
NFPA 704
3
2 0

tert-Butyl methyl ether price More Price(79)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich MX0826 Methyl-t-Butyl Ether OmniSolv? 1634-04-4 1L $159 2024-03-01 Buy
Sigma-Aldrich MX0819 Methyl-t-Butyl Ether Meets ACS Specifications GR ACS 1634-04-4 4L $385 2024-03-01 Buy
Sigma-Aldrich MX0826 Methyl-t-Butyl Ether OmniSolv? 1634-04-4 4L $503 2024-03-01 Buy
Sigma-Aldrich MX0819 Methyl-t-Butyl Ether Meets ACS Specifications GR ACS 1634-04-4 20L $1080 2024-03-01 Buy
Sigma-Aldrich MX0819 Methyl-t-Butyl Ether Meets ACS Specifications GR ACS 1634-04-4 200L $5460 2024-03-01 Buy
Product number Packaging Price Buy
MX0826 1L $159 Buy
MX0819 4L $385 Buy
MX0826 4L $503 Buy
MX0819 20L $1080 Buy
MX0819 200L $5460 Buy

tert-Butyl methyl ether Chemical Properties,Uses,Production

Description

Methyl tert-butyl ether (MTBE) is a colorless liquid with a distinctive, disagreeable odor. It is made from blending chemicals such as isobutylene and methanol, and has been used since the 1980s as an additive for unleaded gasolines to achieve more efficient burning.MTBE is also used to dissolve gallstones. Patients treated in this way have MTBE delivered directly to their gall bladders through special tubes that are surgically inserted. tert-Butyl methyl ether liquid

Chemical Properties

tert-Butyl methyl ether, also known as MTBE or Methyl tert-butyl ether, is a clear, colorless liquid with a low viscosity that is combustible and has a distinct, turpentine-like odor. It is miscible with organic solvents, but only slightly soluble in water. Methyl tert-butyl ether is very stable under alkaline, neutral, and weakly acidic conditions. In the presence of strong acids, it is cleaved to methanol and isobutene. Depending on reaction conditions the latter can form isobutene oligomers. MTBE does not undergo autoxidation and, in contrast to other ethers, it does not form peroxides with atmospheric oxygen. It improves the antiknock properties when added to motor gasoline.

History

tert-Butyl methyl ether was first synthesized (by the classical Williamson ether synthesis) and characterized in 1904. Extensive studies in the United States during World War II demonstrated the outstanding qualities of MTBE as a high-octane fuel component. It was first commercially produced in Italy in 1973 for use as an octane enhancer in gasoline. U.S. production of MTBE started in 1979 after Atlantic Richfield Co. (ARCO) was granted a waiver by the U.S. Environmental Protection Agency (EPA) that allowed MTBE to be blended up to 7 vol % in U.S. unleaded gasoline. The use of other aliphatic ethers was allowed when the U.S. EPA issued its “substantially similar” definition for unleaded gasoline specifications in 1981. Under this definition, any aliphatic ether or ether mixture could be blended in unleaded gasoline as long as the total oxygen contribution from the ethers does not exceed 2.0% oxygen by weight in the gasoline. This allowed MTBE to be blended up to approximately 11 vol % in gasoline.

Uses

Methyl tert-butyl ether (MTBE) was primarily used as a gasoline additive in unleaded gasoline in the United States prior to 2005, in the manufacture of isobutene, and as a chromatographic eluent especially in high pressure liquid chromatography. It is also a pharmaceutical agent and can be injected into the gallbladder to dissolve gallstones (ATSDR, 1996). tert-Butyl methyl ether is also used in the petrochemical industry. By reversal of its formation reaction, MTBE can be cracked to isobutene and methanol on acidic catalysts at higher temperature than MTBE synthesis.

Preparation

tert-butyl methyl ether can be prepared by the reaction of potassium tert-butoxide and bromomethane. Methyl tert-butyl ether also can be obtained by the acid-catalyzed addition of methanol to isobutene. Suitable catalysts are solid acids such as bentonites, zeolites and – commonly used in industrial world scale MTBE-production units – macroporous acidic ion-exchange resins. The reaction is weakly exothermic with a heat of reaction of -37.7 kJ/mol.
preparation of tert-butyl methyl ether

Definition

ChEBI: Methyl tert-butyl ether is an ether having methyl and tert-butyl as the two alkyl components. It has a role as a non-polar solvent, a fuel additive and a metabolite.

General Description

Methyl tert-butyl ether appears as a colorless liquid with a distinctive anesthetic-like odor. Vapors are heavier than air and narcotic (cause drowsiness when inhaled). This liquid has a flash point lower than most ambient temperatures, so it will readily ignite under most conditions. It is less dense than water and moderately soluble in water. Used as a octane booster in gasoline.

Air & Water Reactions

Highly flammable. Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick 1979. p.151-154, 164]. A mixture of liquid air and diethyl ether exploded spontaneously [MCA Case History 616. 1960].

Reactivity Profile

Tert-Butyl methyl ether is a kind of Ethers, it form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

Hazard

Tert-Butyl methyl ether is slightly toxic by ingestion and inhalation. Flammable when exposed to heat or flame. Upper respiratory tract irritant and kidney damage. Questionable carcinogen.

Health Hazard

INHALATION: May cause dizziness or suffocation. Contact may irritate or burn eyes or skin. May be harmful if swallowed.

Industrial uses

Methyl tert-butyl ether (MTBE) is used as an octane enhancer in gasoline. EPA regulations allow up to 2.7 wt.% oxygen in gasoline which allows 15 vol.% MTBE in gasoline. Other alkyl ethers can also be blended into gasoline up to the 2.7 wt% oxygen requirement. The stability of MTBE to oxidation and peroxide formation gives this unsymmetrical ether an advantage over other ethers in various extraction and reaction solvent applications.

Safety Profile

Poison by intravenous route. Slightly toxic by ingestion and inhalation. Flammable when exposed to heat or flame. When heated to decomposition it emits acrid smoke and irritating fumes. See also ETHERS.

Potential Exposure

Tert-Butyl methyl ether is used as an organic solvent; as an octane booster in unleaded gasolines; in making other chemicals; and in medicine to dissolve gall stones

First aid

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.

Carcinogenicity

EPA has not classified methyl tert-butyl ether with respect to potential carcinogenicity. There is evidence for the carcinogenicity of MTBE in animals. MTBE causes leukemias/lymphomas in female rats, renal tubular tumors and Leydig cell tumors in male rats, and hepatocellular tumors in mice. Positive animal carcinogenicity data and some further concordance in tumor sites for formaldehyde and TBA, metabolites of MTBE, provide support for this conclusion. However, uncertainties remain about the nature and extent of risk at very low doses, and about the particular tumor sites that are most relevant to humans.

Environmental Fate

tert-Butyl Methyl Ether can be released during manufacturing or blending with gasoline; during the storage, distribution, and transfer of MTBE-blended gasoline; and from spills or leaks or fugitive emissions at automotive service stations (U.S. EPA, 1994a). Vapor emissions from MTBE-blended gasoline may also contribute to atmospheric levels (U.S. EPA, 1988). It is not expected to persist in the atmosphere because it undergoes destruction from reactions with hydroxyl radicals. A total atmospheric lifetime for MTBE of approximately 3 and 6.1 days has been reported in polluted urban air and in nonpolluted rural air, respectively (U.S. EPA, 1993a). Based upon its vapor pressure and Henry s law constant, MTBE is highly volatile and would be expected to evaporate rapidly from soil surfaces or water. It may be fairly persistent when introduced into subsurface soils or to groundwater since volatilization to the atmosphere is reduced or eliminated. It does not readily degrade in surface waters due to hydrolysis or other abiotic processes. It is also resistant to biodegradation (U.S. EPA, 1993a). It is usually removed from surface waters very rapidly because of its high volatility. If released as part of a gasoline mixture from leaking underground storage tanks, its relatively high water solubility combined with little tendency to sorb to soil particles encourages migration to local groundwater supplies (U.S. EPA, 1993a).

Shipping

UN2398 Methyl tert-butyl ether, Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Purify as for n-butyl methyl ether. [Beilstein 1 IV 1615.]

Incompatibilities

May form explosive mixture with air. May be able to form unstable peroxides. Much less likely to form peroxides than other ethers. Incompatible with strong acids. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. May accumulate static electrical charges, and cause ignition of its vapors.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

67-56-1
115-11-7
1634-04-4
Synthesis of tert-Butyl methyl ether from Methanol and Isobutylene
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Methyl-tert-bu tert-Butyl methyl ether for HPLC, >=99.8% tert-Butyl methyl ether HPLC Plus, for HPLC, GC, and residue analysis, 99.9% tert-Butyl methyl ether puriss. p.a., >=99.5% (GC) tert-Butyl methyl ether reagent grade, >=98% tert-Butyl Methyl ether ACS reagent, >=99.0% tert-Butyl Methyl ether, 99%, SpcDry, Water≤50 ppM (by K.F.), SpcSeal N-ALPHA-T-BOC-NG-(4-METHOXY-2,3,6 TRIMETHYLBENZENESULFONYL)-L-ARGININE N-ALPHA-TERT-BUTYLOXYCARBONYL-N'-(4-METHOXY-2,3,6-TRIMETHYLPHENYL-SULFONYL)-L-ARGININE N-ALPHA-T-BUTOXYCARBONYL-N-OMEGA-4-METHOXY-2,3,6-TRIMETHYLBENZENESULFONYL-L-ARGININE N-ALPHA-BOC-N(G)-4-METHOXY-2,3,6-TRIMETHYLBENZENESULFONYL-L-ARGININE N-ALPHA-BOC-N-OMEGA-(4-METHOXY-2,3,6-TRIMETHYL-BENZENE-SULFONYL)-L-ARGININE TERT-BUTYL METHYL ETHER T-BUTYL METHYL ETHER 300 TBOC-L-ARGININE (MTR) METHYLTERT-BUTYLETHER,HPLCGRADE METHYLTERT-BUTYLETHER,OMNISOLV METHYLTERT-BUTYLETHER,PESTISOLV METHYLTERT-BUTYLETHER,REAGENT tert-Butyl methyl ether, extra dry over mol. sieve tert-Butyl methyl ether, extra pure, 99.9% tert-Butyl methyl ether, pure, 99% METHYL tert-BUTYL ETHER DISTILLED IN GLASS METHYL tert-BUTYL ETHER HPLC METHYL tert-BUTYL ETHER REAGENT (ACS) methyl tert-butyl ether solution tert-butyl methyl ether solution tert-butylmethyl ether, hplc grade (2-Methyl-2-propyl)methylether 1,1-dimethyl-1-methoxyethane 1,1-dimethylethylmethylether TERT-BUTYL METHYL ETHER 99.7% A.C.S. & TERT-BUTYL METHYL ETHER FOR RESIDUE & TERT-BUTYL METHYL ETHER, 99+%, PRA GRADE TERT.-BUTYL METHYL ETHER DRIED (MAX.0,00 75 % H2O), R. G. TERT.-BUTYL METHYL ETHER R. G. TERT.-BUTYL METHYL ETHER SPECTRANAL TERT-BUTYL METHYL ETHER TECHNICAL 5 L TERT-BUTYL METHYL ETHER FOR GC TERT-BUTYL METHYL ETHER, ANHYDROUS, 99.8 % METHYL T-BUTYL ETHER GC STANDARD Tert-ButylMethylEtherGr MethylT-ButylEtherAcs Tert-ButylMethylEtherForSynthesis tert-Butyl methyl ether, HPLC Grade, 99+% tert-Butyl methyl ether, HPLC grade, 99+%, packaged under Argon in resealable ChemSealTM bottles tert-Butyl Methyl Ether (1mg/ml in Methanol) [for Water Analysis] tert-Butyl methyl ether, reagent grade tert-Butyl methyl ether, for GC residue analysis tert-Butyl methyl ether, for ultra-trace analysis (capillary chromatography) tert-Butyl methyl ether, anhydrous, 99,5% tert-Butyl methyl ether, anhydrous, with molecular sieves tert-Butyl methyl ether 1g [1634-04-4] METHYL tert-BUTYL ETHER DISTILLED IN GLASS (MTBE) METHYL tert-BUTYL ETHER REAGENT (ACS), MTBE METHYL tert-BUTYL ETHER HPLC, (MTBE) tert-Butyl methyl et tert-Butyl methyl ether, for spectroscopy, 99.8%