295035
1,3-Butadiene
≥99%
Sinónimos:
Bivinyl, Vinylethylene, alpha,gamma-Butadiene
About This Item
Productos recomendados
vapor density
1.9 (15 °C, vs air)
Quality Level
vapor pressure
1863 mmHg ( 21 °C)
assay
≥99%
autoignition temp.
788 °F
contains
p-tert-butylcatechol as inhibitor
expl. lim.
12 %
bp
−4.5 °C (lit.)
mp
−109 °C (lit.)
solubility
water: soluble 0.5 g/L at 20 °C
density
0.62 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
C=CC=C
InChI
1S/C4H6/c1-3-4-2/h3-4H,1-2H2
InChI key
KAKZBPTYRLMSJV-UHFFFAOYSA-N
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General description
Application
It may be used in the synthesis of the following:
- 1-Silyl-substituted 1,3-butadienes, by [RuHCl(CO)(PCy3)2]-catalyzed silylative coupling of terminal (E)-1,3-dienes with vinylsilanes.
- Synthetic rubber and thermoplastic resins.
- Disilylated dimers by reacting with chlorosilanes.
- Octa-2,7-dien-1-ol via palladium catalyzed-hydrodimerization.
Biochem/physiol Actions
Packaging
Compatible with the following:
Legal Information
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also commonly purchased with this product
hose barb
regulator
signalword
Danger
hcodes
Hazard Classifications
Flam. Gas 1A - Muta. 1B - Press. Gas Liquefied gas
Storage Class
2A - Gases
wgk_germany
WGK 3
flash_point_f
-104.8 °F - closed cup
flash_point_c
-76 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Artículos
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
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