1-Butene

But-1-ene is an alkene easily condensed to give a colorless liquid.It is classified as a linear alpha-olefin (terminal alkene).Polymerization of but-1-ene gives polybutylene, which is used to make piping for domestic plumbing.[4] It has also been used as a precursor to polypropylene resins, butylene oxide, and butanone.[5] But-1-ene is produced by separation from crude C4 refinery streams and by ethylene dimerization.
NFPA 704 four-colored diamond Health 1: Exposure would cause irritation but only minor residual injury. E.g. turpentine Flammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propane Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code
Preferred IUPAC nameCAS NumberBeilstein ReferenceChEMBLChemSpiderECHA InfoCardEC NumberGmelin ReferencePubChemUN numberCompTox DashboardSMILESChemical formulaMolar massDensityMelting pointBoiling pointSolubility in waterSolubilityalcoholbenzeneRefractive indexViscosityGHS labellingPictogramsHazard statementsPrecautionary statementsNFPA 704Flash pointAutoignitiontemperatureExplosive limitsstandard stateorganic compoundalpha-olefinisomersbutenepolybutylenecomonomerlinear low-density polyethylenebutylene oxidebutanoneethylene dimerization2-butenesThe Royal Society of ChemistryUllmann's Encyclopedia of Industrial ChemistryAlkenesEthenePropenePenteneHexeneHepteneOcteneNoneneDeceneDehydrohalogenationhaloalkaneDehydration reactionSemihydrogenationalkyneBamford–Stevens reactionBarton–Kellogg reactionBoord olefin synthesisChugaev eliminationCope reactionCorey–Winter olefin synthesisGrieco eliminationHofmann eliminationHorner–Wadsworth–Emmons reactionHydrazone iodinationJulia olefinationKauffmann olefinationMcMurry reactionPeterson olefinationRamberg–Bäcklund reactionShapiro reactionTakai olefinationWittig reactionOlefin metathesisEne reactionCope rearrangementHydrogenationHalogenationHydrationElectrophilic additionOxymercuration reactionHydroborationCyclopropanationEpoxidationDihydroxylationOzonolysisHydrohalogenationPolymerizationDiels–Alder reactionWacker processDehydrogenationFriedel-Crafts AlkylationBinary compounds of hydrogenGroup 13 hydridesBoranesB10H14B18H22NihonanesGroup 14 hydridesHydrocarbonsalkanesalkynesCycloalkanesCycloalkenesCycloalkynesAnnulenesSilanesSi4H10Si5H12Si6H14more...SilenesStannanesFlerovanesPnictogen (Group 15) hydridesAzanesAzenesPhosphenesArsanesHydrogen chalcogenides (Group 16 hydrides)PolyoxidanesPolysulfanesSelanesHydrogen halides (Group 17 hydrides)Transition metal hydridesPdHx (x < 1)Exotic matter hydrides