- 2,2,3-Trimethylbutane
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- $0.00 / 1000kg
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2024-08-15
- CAS:464-06-2
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 20tons
- 2,2,3-TRIMETHYLBUTANE
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- $0.10 / 1KG
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2019-12-25
- CAS:464-06-2
- Min. Order: 1KG
- Purity: 95%-99%
- Supply Ability: 1kg; 100kg; 1000kg
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| 2,2,3-TRIMETHYLBUTANE Basic information |
Product Name: | 2,2,3-TRIMETHYLBUTANE | Synonyms: | 2,2,3-TRIMETHYLBUTANE;2,3,3-TRIMETHYLBUTANE;PENTAMETHYLETHANE;TRIPTANE;2,2,3-trimethyl-butan;butane,2,2,3-trimethyl-;isopropyltrimethylmethane;trimethylbutane(non-specificname) | CAS: | 464-06-2 | MF: | C7H16 | MW: | 100.2 | EINECS: | 207-346-3 | Product Categories: | | Mol File: | 464-06-2.mol | |
| 2,2,3-TRIMETHYLBUTANE Chemical Properties |
Melting point | −25 °C(lit.) | Boiling point | 80.9 °C(lit.) | density | 0.69 g/mL at 25 °C(lit.) | vapor pressure | 3.37 psi ( 37.7 °C) | refractive index | n20/D 1.389(lit.) | Fp | 20 °F | form | Liquid | color | Clear colorless | explosive limit | ~7% | Water Solubility | 4.38mg/L at 25℃ | BRN | 1730756 | Dielectric constant | 1.9(20℃) | LogP | 3.59 | CAS DataBase Reference | 464-06-2(CAS DataBase Reference) | EPA Substance Registry System | 2,2,3-Trimethylbutane (464-06-2) |
| 2,2,3-TRIMETHYLBUTANE Usage And Synthesis |
Description | 2,2,3-Trimethylbutane (i.e., triptane) is a potential gasoline octane booster with a research octane number (RON) of 112. it is also used as a fuel additive and in comparative rate of thermal decomposition (CRTD) single-pulse surge tube studies[1-2]. | Chemical Properties | Colorless liquid. Soluble in alcohol;
insoluble in water. | Uses | Organic synthesis, aviation fuel. | Preparation | 2,2,3-Trimethylbutane (triptane) selectively forms from dimethyl ether at low temperatures on acid zeolites[3]. We report herein the first selective catalytic conversion of DME to
triptane on halide-free catalysts,
specifically on crystalline solid
acids, at much lower reaction temperatures (453–493 K) and higher
DME pressures (60–250 kPa) than
in established methanol/DME to
hydrocarbon processes. Low temperatures avoid intervening skeletal
isomerization and b-scission of triptyl chains or their precursors. These
processes would otherwise occur
before the methylation events that
form the C7 chains containing the
triptane backbone, which desorb irreversibly as triptane.
| Synthesis Reference(s) | Tetrahedron Letters, 21, p. 3151, 1980 DOI: 10.1016/S0040-4039(00)77432-6 | Hazard | Flammable, moderate fire risk. | References | [1] NOUR ATEF. Chemical kinetic study of triptane (2,2,3-trimethylbutane) as an anti-knock additive[J]. Combustion and Flame, 2019. DOI:10.1016/j.combustflame.2019.09.006. [2] TSANG W. Comparative rate single-pulse shock tube studies on the thermal decomposition of cyclohexene, 2,2,3-trimethylbutane, isopropyl bromide, and ethylcyclobutane[J]. International Journal of Chemical Kinetics, 1970. DOI:10.1002/kin.550020406. [3] JOHN?H. AHN; Enrique I Prof; Burcin Temel Dr. Selective Homologation Routes to 2,2,3-Trimethylbutane on Solid Acids?[J]. Angewandte Chemie International Edition, 2009. DOI:10.1002/anie.200900541.
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| 2,2,3-TRIMETHYLBUTANE Preparation Products And Raw materials |
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