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295035

Sigma-Aldrich

1,3-Butadiene

≥99%

Sinônimo(s):

Bivinyl, Vinylethylene, alpha,gamma-Butadiene

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About This Item

Fórmula linear:
CH2=CHCH=CH2
Número CAS:
Peso molecular:
54.09
Beilstein:
605258
Número CE:
Número MDL:
Código UNSPSC:
12142100
ID de substância PubChem:
NACRES:
NA.22

densidade de vapor

1.9 (15 °C, vs air)

Nível de qualidade

pressão de vapor

1863 mmHg ( 21 °C)

Ensaio

≥99%

temperatura de autoignição

788 °F

contém

p-tert-butylcatechol as inhibitor

Lim. expl.

12 %

p.e.

−4.5 °C (lit.)

pf

−109 °C (lit.)

solubilidade

water: soluble 0.5 g/L at 20 °C

densidade

0.62 g/mL at 20 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

C=CC=C

InChI

1S/C4H6/c1-3-4-2/h3-4H,1-2H2

chave InChI

KAKZBPTYRLMSJV-UHFFFAOYSA-N

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Descrição geral

1,3-Butadiene (BD) is a simplest conjugated diene. It is a colorless gas that turns to liquid easily. The vapor phase conversion of ethanol in the presence of Cr-Ba/MCM-41 (mesoporous silica molecular sieve) catalyst reported a yield of 25% of BD. It is also formed as a coproduct of ethylene production. Mechanism of Diels-Alder reaction of 1,3-butadiene with ethylene has been investigated.
May contain up to 4% dimer impurity.

Aplicação

1,3-Butadiene can undergo a four-component coupling reaction with aryl Grignard reagents, and alkyl fluorides in the presence of nickel catalyst to form 1,6-octadiene carbon compound substituted with alkyl and aryl groups at the 3- and 8-positions.
1,3-Butadiene is a useful diene for Diels Alder reaction.
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.

Ações bioquímicas/fisiológicas

1,3-Butadiene has been reported to induce hemangiosarcomas of the heart, malignant lymphomas, alveolar-bronchiolar neoplasms, squamous cell neoplasms of the forestomach in males and female mice. It also induced acinar cell carcinomas of the mammary gland, granulosa cell neoplasms of the ovary, and hepatocellular neoplasms in female mice. Carcinogenicity induced by inhaled 1,3-butadiene has been investigated in C57BL/6 x C3H F1 mice.
Environmental carcinogen. Induces cardiac hemangiosarcomas in mice.

Embalagem

Supplied in a Sure/Pac cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

Informações legais

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

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Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Flam. Gas 1A - Muta. 1B - Press. Gas Liquefied gas

Código de classe de armazenamento

2A - Gases

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

-104.8 °F - closed cup

Ponto de fulgor (°C)

-76 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)


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Visite a Biblioteca de Documentos

Palladium-Catalyzed Dimerization Disilylation of 1,3-Butadiene with Chlorosilanes.
Terao J, et al.
Organic Letters, 6(19), 3341-3344 (2004)
Carcinogenicity of 1,3-butadiene in C57BL/6 x C3H F1 mice at low exposure concentrations.
Melnick RL, et al.
Cancer Research, 50, 6592-6599 (1990)
Selective catalytic hydrodimerization of 1, 3-butadiene by palladium compounds dissolved in ionic liquids.
Dullius JEL, et al.
Organometallics, 17(5), 815-819 (1998)
Nickel-catalyzed coupling reaction of alkyl halides with aryl Grignard reagents in the presence of 1, 3-butadiene: Mechanistic studies of four-component coupling and competing cross-coupling reactions.
Iwasaki T, et al.
Chemical Science (2018)
J E Huff et al.
Science (New York, N.Y.), 227(4686), 548-549 (1985-02-01)
Groups of 50 male and 50 female B6C3F1 mice were exposed 6 hours per day, 5 days per week, for 60 to 61 weeks to air containing 0, 625, or 1250 parts per million 1,3-butadiene. These concentrations are somewhat below

Artigos

The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. Since the reaction involves the formation of a cyclic product via a cyclic transition state, it is also referred to as a "cycloaddition".

Protocolos

2-Butene; 2-Methylbutane; 1,3-Butadiene; Propyne

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