2,3-DIMETHYL-1,3-BUTADIENE

2,3-DIMETHYL-1,3-BUTADIENE
  • CAS No.:513-81-5
Other grades of this product :
2,3-DIMETHYL-1,3-BUTADIENE Basic information
Product Name:2,3-DIMETHYL-1,3-BUTADIENE
Synonyms:2,3-Dimethyl-1,3-butadiene - stab with BHT;2,3-dimethyl-3-butadiene;2,3-Dimethylbutadiene;2,3-Dimethylenebutane;2,3-Dimethylerythrene,Diiso-propenyl;2,3-DIMETHYL-BUTA-1,3-DIENE;2,3-DIMETHYL-1,3-BUTADIENE;Biisopropenyl
CAS:513-81-5
MF:C6H10
MW:82.14
EINECS:208-172-0
Product Categories:Acyclic;Alkenes;DID - DINChemical Class;NeatsGasoline, Diesel,&Petroleum;Substance classes;Organic Building Blocks;Alpha Sort;D;DAlphabetic;Hydrocarbons;Olefins;Volatiles/ Semivolatiles
Mol File:513-81-5.mol
2,3-DIMETHYL-1,3-BUTADIENE Chemical Properties
Melting point -76 °C (lit.)
Boiling point 68-69 °C (lit.)
density 0.726 g/mL at 25 °C (lit.)
vapor pressure 269 mm Hg ( 37.7 °C)
refractive index n20/D 1.438(lit.)
Fp −8 °F
storage temp. 2-8°C
form Liquid
color Clear colorless
Water Solubility Miscible with chloroform. Immiscible with water.
Merck 14,3238
BRN 605285
CAS DataBase Reference513-81-5(CAS DataBase Reference)
EPA Substance Registry System1,3-Butadiene, 2,3-dimethyl- (513-81-5)
Safety Information
Hazard Codes F
Risk Statements 11
Safety Statements 16-23
RIDADR UN 3295 3/PG 2
WGK Germany 3
9
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29012900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2,3-DIMETHYL-1,3-BUTADIENE Usage And Synthesis
Chemical PropertiesClear colorless liquid
Uses2,3-Dimethyl-1,3-butadiene undergoes Diels Alder cycloaddition reaction and it also participates in polymerization reactions. It is also involved in manufacturing of synthetic rubber.
General Description2,3-Dimethyl-1,3-butadiene (DMBD) is a conjugated diene. It undergoes Diels Alder cycloaddition reaction with 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions. It undergoes thermal [4+2] cycloaddition reaction with 3-acetyl-, 3-carbamoyl and 3-ethoxycarbonylcoumarins under solvent free conditions. DMBD participates in polymerization reactions in the presence of iron dichloride complexes based catalysts.
Purification MethodsDistil it from NaBH4, and purify it by zone melting. [Beilstein 1 IV 1023.]

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