TRANS-2-PENTENE

TRANS-2-PENTENE Basic information
Product Name:TRANS-2-PENTENE
Synonyms:SYM-METHYLETHYLETHYLENE;TRANS-2-AMYLENE;TRANS-2-PENTENE;TRANS-SYM-METHYLETHYLETHYLENE;TRANS-B-N-AMYLENE;(2E)-2-Pentene;(E)-2-Pentene;2-(E)-C5H10
CAS:646-04-8
MF:C5H10
MW:70.13
EINECS:211-461-4
Product Categories:Acyclic;Alkenes;Organic Building Blocks;Alpha Sort;P;PA - PEN;P-SAlphabetic;Volatiles/ Semivolatiles
Mol File:646-04-8.mol
TRANS-2-PENTENE Structure
TRANS-2-PENTENE Chemical Properties
Melting point -140 °C (lit.)
Boiling point 37 °C (lit.)
density 0.649 g/mL at 25 °C (lit.)
vapor pressure 8.06 psi ( 20 °C)
refractive index n20/D 1.381
Fp −50 °F
storage temp. 2-8°C
solubility Soluble in alcohol, benzene, and ether (Weast, 1986)
pka>14 (Schwarzenbach et al., 1993)
form clear liquid
color cis Form: Liquid
Water Solubility 203 mg/kg at 25 °C (shake flask-GC, McAuliffe, 1966)
Merck 14,7123
BRN 1718795
Henry's Law Constant0.234 at 25 °C (Hine and Mookerjee, 1975)
LogP2.580 (est)
CAS DataBase Reference646-04-8(CAS DataBase Reference)
EPA Substance Registry Systemtrans-2-Pentene (646-04-8)
Safety Information
Hazard Codes F,Xn
Risk Statements 11-36/37/38-65
Safety Statements 9-16-26-29-33-36-62
RIDADR UN 3295 3/PG 2
WGK Germany 3
RTECS SB2184500
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29012900
Hazardous Substances Data646-04-8(Hazardous Substances Data)
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
TRANS-2-PENTENE Usage And Synthesis
Chemical Propertiesclear colourless to slightly yellowish liquid
Physical propertiesClear, colorless, very flammable liquid with a disagreeable odor.
UsesPolymerization inhibitor; organic synthesis.
Usestrans-2-Pentene has been used for the calculation of OH levels by the decay method.
General DescriptionColorless liquid with a hydrocarbon odor. Usually in technical grade as a mixture of isomers. Used as a solvent, in organic synthesis, and as a polymerization inhibitor.
Air & Water ReactionsHighly flammable. Insoluble in water.
Reactivity ProfileThe unsaturated aliphatic hydrocarbons, such as 2-PENTENE, are generally much more reactive than the alkanes. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions.
Safety ProfileA dangerous fire and explosion hazard when exposed to heat or flame; can react vigorously with oxidizing materials. When heated to decomposition it emits acrid smoke and irritating fumes.
SourceSchauer et al. (1999) reported trans-2-pentene in a diesel-powered medium-duty truck exhaust at an emission rate of 50 μg/km.
Schauer et al. (2001) measured organic compound emission rates for volatile organic compounds, gas-phase semi-volatile organic compounds, and particle-phase organic compounds from the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emission rate of trans-2-pentene was 16.0 mg/kg of pine burned. Emission rates of trans-2-pentene were not measured during the combustion of oak and eucalyptus.
California Phase II reformulated gasoline contained trans-2-pentene at a concentration of 4.12 g/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without catalytic converters were 0.71 and 77.4 mg/km, respectively (Schauer et al., 2002).

Environmental fateChemical/Physical. Complete combustion in air yields carbon dioxide and water.
Purification MethodsIt is treated as above and washed with water, dried over anhydrous Na2CO3, and fractionally distilled. The middle cut is purified by two passes of fractional melting. [Beilstein 1 IV 814.]
TRANS-2-PENTENE Preparation Products And Raw materials
Raw materialsETHYLCYCLOPROPANE-->Methylcyclobutane.
Preparation Products4-Methylenenonane-->CIS-2-PENTENE-->TRANS-1,3-PENTADIENE-->N,N-DIMETHYLHEXYLAMINE-->2-CHLOROPENTANE-->CIS-1,3-PENTADIENE
4-Methyl-trans-2-pentene Mesityl oxide 4-methyl-3-ethyl-trans-2-pentene 2,2-Dimethyl-4-pentenoic acid 4-Penten-1-ol CIS-3-METHYL-2-PENTENE 1-(Trimethylsiloxy)cyclopentene 2,4-DIMETHYL-2-PENTENOIC ACID TRANS-2-PENTEN-1-OL 4-CYCLOPENTENE-1,3-DIONE 3-PENTENOIC ACID Methyl (E)-3-pentenoate ETHCHLORVYNOL CIV (0.7 ML) 1,5-BIS(2-METHYL-5-CHLORO-3-THIENYL)CYCLOPENTENE METHYL 2-PENTENOATE 4-PENTENENITRILE 4-PENTEN-2-OL 4,4-Dimethyl-trans-2-pentene

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