Interesting facts
Interesting Facts about Buta-1,3-diene
Buta-1,3-diene is a fascinating compound with a variety of applications and properties that make it essential in the field of chemistry and industrial processes. Here are some intriguing aspects of this diene:
- Structure: Buta-1,3-diene is an example of a conjugated diene, meaning it possesses double bonds that are separated by a single bond. This unique structure allows for resonance stabilization and plays a crucial role in its reactivity.
- Polymer Production: One of the most significant uses of buta-1,3-diene is in the production of synthetic rubber, specifically styrene-butadiene rubber (SBR) and polybutadiene. These materials are integral to many products, from tires to footwear.
- Reactivity: Buta-1,3-diene undergoes various chemical reactions, including electrophilic addition and polymerization. Its ability to form stable radical intermediates enhances its utility in organic synthesis.
- Sources: It can be produced from natural sources, particularly from the cracking of petroleum. This highlights the compound's connection to both natural processes and synthetic chemistry.
- Energy and Fuel: There is ongoing research into the use of buta-1,3-diene as a potential biofuel and energy source, showcasing its relevance in the context of renewable energy.
As noted by chemists, "the innovation in using simple hydrocarbons can lead to significant advancements in material sciences and energy solutions." This encapsulates the importance of buta-1,3-diene in modern chemistry.
In summary, buta-1,3-diene's unique characteristics and versatile applications make it a remarkable compound in both academic and industrial chemistry, and the exploration of its properties continues to yield exciting discoveries.
Synonyms
1,3-BUTADIENE
Buta-1,3-diene
106-99-0
Divinyl
BUTADIENE
Biethylene
Vinylethylene
Erythrene
Bivinyl
Pyrrolylene
Butadieen
Butadien
Buta-1,3-dien
Buta-1,3-dieen
alpha,gamma-Butadiene
Butadiene monomer
NCI-C50602
1,3-butadien
Butadiene-1,3-uninhibited
Buta-1,3-dien [German]
CCRIS 99
Butadiene, 1,3-
HSDB 181
JSD5FGP5VD
.alpha.,.gamma.-Butadiene
EINECS 203-450-8
CHEBI:39478
UNII-JSD5FGP5VD
1,3-BUTADIENE-2,3-D2
CH2=CHCH=CH2
CH2=CH-CH=CH2
UN 1010
1,3-Butadiene (ca. 15% in Toluene)
DTXSID3020203
MFCD00008659
130983-70-9
25339-57-5
1,3-Butadiene (ca. 15% in Hexane)
EC 203-450-8
1983-06-8
1,3-BUTADIENE (IARC)
1,3-BUTADIENE [IARC]
vinyl ethylene
Polybutadiene, cis
1,3 butadiene
Butadieen [Dutch]
Butadien [Polish]
26952-74-9
alpha-gamma-butadiene
1,3-Butadiene, puriss., >=99.5% (GC)
Buta-1,3-dieen [Dutch]
butadiene-1,3
alpha, gamma-butadiene
1,3-Butadiene 95%
alpha,<<gamma>>-Butadiene
CH22CH1CH2CH2
BUTADIENES, STABILIZED
DTXCID10203
1,3-Butadiene, >=99%
1,3-BUTADIENE [MI]
CHEMBL537970
1,3-BUTADIENE [HSDB]
CHEBI:39479
1,3-Butadiene, >=99.6%
BUTADIENE-1, 3, STABILIZED
1,3-BUTADIENE, (STABILIZED)
1,3-Butadiene, purum, >=98.0%
AKOS007930655
1,3-Butadiene 100 microg/mL in Methanol
1,3-Butadiene 200 microg/mL in Methanol
1,3-Butadiene 1000 microg/mL in Methanol
B0675
B4358
B4359
B4835
NS00007558
1,3-Butadiene 10000 microg/mL in Methanol
InChI=1/C4H6/c1-3-4-2/h3-4H,1-2H
Q161503
1,3-Butadiene (~15per cent by weight in Toluene)
1,3-Butadiene 10 microg/mL in N,N-Dimethylacetamide
1,3-Butadiene 50 microg/mL in N,N-Dimethylacetamide
1,3-Butadiene 150 microg/mL in N,N-Dimethylacetamide
1,3-Butadiene 250 microg/mL in N,N-Dimethylacetamide
1,3-Butadiene 400 microg/mL in N,N-Dimethylacetamide
1,3-Butadiene (ca. 13% in Tetrahydrofuran, ca. 2mol/L)
203-450-8
Solubility of Buta-1,3-diene
Buta-1,3-diene, with the chemical formula C4H6, exhibits unique solubility characteristics owing to its structure as a conjugated diene. This hydrocarbon is generally considered to have limited solubility in water, which can be attributed to:
In summary, while buta-1,3-diene lacks appreciable solubility in aqueous solutions, its affinity for non-polar media makes it suitable for various applications in organic chemistry. As a rule of thumb, remember the phrase: "Like dissolves like."