2,3-DIMETHYL-1,3-BUTADIENE

2,3-DIMETHYL-1,3-BUTADIENE Basic information
Product Name:2,3-DIMETHYL-1,3-BUTADIENE
Synonyms:2,3-dimethyl-3-butadiene;2,3-Dimethylenebutane;2,3-Dimethylerythrene,Diiso-propenyl;2,3-DIMETHYL-BUTA-1,3-DIENE;2,3-DIMETHYL-1,3-BUTADIENE;Biisopropenyl;CH2=C(CH3)C(CH3)=CH2;Diisopropenyl
CAS:513-81-5
MF:C6H10
MW:82.14
EINECS:208-172-0
Product Categories:Acyclic;Alkenes;Organic Building Blocks;DID - DINChemical Class;NeatsGasoline, Diesel,&Petroleum;Substance classes;Alpha Sort;D;DAlphabetic;Hydrocarbons;Olefins;Volatiles/ Semivolatiles
Mol File:513-81-5.mol
2,3-DIMETHYL-1,3-BUTADIENE Structure
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.]
M-CRESOL PURPLE, SODIUM SALT 2,3-DIMETHYL-1,3-BUTADIENE-D10 ETHYLTETRAMETHYLCYCLOPENTADIENE 2,5-Dimethyl-3,4-diphenylcyclopentadienone COOMASSIE BLUE GL CITRININ 1,2,3,4,5-PENTAPHENYL-1,3-CYCLOPENTADIENE 5-Carbethoxy-4,6-dimethyl-2-pyrone 2,3-DIMETHYL-1,3-BUTADIENE Colchicine 2,5-DIETHYL-3,4-DIPHENYLCYCLOPENTADIENONE 1,2,3,4-TETRAPHENYL-1,3-CYCLOPENTADIENE Methyl isodehydroacetate 1,2,3,4,5-Pentamethylcyclopentadiene PENTAMETHYL CYCLOPENTADIENE-1,2,3,4,5-PENTACARBOXYLATE Guaiazulene Tetraphenylcyclopentadienone METHYLTHYMOL BLUE PENTASODIUM SALT

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