1-Hexyne

1-Hexyne
  • CAS No.:693-02-7
Other grades of this product :
1-Hexyne Basic information
Product Name:1-Hexyne
Synonyms:N-BUTYLACETYLENE;Butylacetylene;C4H9CequivCH;Hex-1-yne;Hexyne;1-HEXYNE;HEXYNE(1-);Butyl acetyne
CAS:693-02-7
MF:C6H10
MW:82.14
EINECS:211-736-9
Product Categories:Miscellaneous;Acetylenes;Acetylenic Hydrocarbons;Alkynes;Organic Building Blocks;Terminal
Mol File:693-02-7.mol
1-Hexyne Chemical Properties
Melting point -132 °C
Boiling point 71-72 °C(lit.)
density 0.715 g/mL at 25 °C(lit.)
vapor pressure 253 mm Hg ( 37.7 °C)
refractive index n20/D 1.399(lit.)
Fp −6 °F
storage temp. Store at +2°C to +8°C.
solubility 0.36g/l (experimental)
form Liquid
Specific Gravity0.715
color Clear colorless
Water Solubility Miscible with organic solvents. Immiscible with water.
BRN 635687
Stability:Stable. Incompatible with strong oxidizing agents. Highly flammable - readily forms explosive mixtures with air.
CAS DataBase Reference693-02-7(CAS DataBase Reference)
NIST Chemistry Reference1-Hexyne(693-02-7)
EPA Substance Registry System1-Hexyne (693-02-7)
Safety Information
Hazard Codes F,Xn,Xi
Risk Statements 11-36/37/38-65
Safety Statements 16-26-36-62-9-33-7/9
RIDADR UN 3295 3/PG 2
WGK Germany 3
RTECS MQ9691000
10-23
Autoignition Temperature263 °C
Hazard Note Irritant
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29012980
MSDS Information
ProviderLanguage
1-Hexyne English
SigmaAldrich English
ACROS English
ALFA English
1-Hexyne Usage And Synthesis
Chemical Propertiescolourless liquid
Uses1-Hexyne is used in the preparation of tricyclic isoindolinone scaffold by undergoing hydrozirconation and ring-closing metathesis. It is used to prepare trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate by reacting with thianthrene cation radical tetrafluoroborate.
General Description1-Hexyne reacted with thianthrene cation radical tetrafluoroborate to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate.
HazardProbably flammable.
Purification MethodsDistil it from NaBH4 to remove peroxides. Stand over sodium for 24hours, then fractionally distil it under reduced pressure. Also dry it by repeated vacuum transfer into freshly activated 4A molecular sieves, followed by vacuum transfer onto Na/K alloy and stirring for 1hour before fractionally distilling. [Beilstein 1 IV 1006.]

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