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295035

Sigma-Aldrich

1,3-Butadiene

≥99%

Sinonimo/i:

Bivinyl, Vinylethylene, alpha,gamma-Butadiene

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About This Item

Formula condensata:
CH2=CHCH=CH2
Numero CAS:
Peso molecolare:
54.09
Beilstein:
605258
Numero CE:
Numero MDL:
Codice UNSPSC:
12142100
ID PubChem:
NACRES:
NA.22

Densità del vapore

1.9 (15 °C, vs air)

Livello qualitativo

Tensione di vapore

1863 mmHg ( 21 °C)

Saggio

≥99%

Temp. autoaccensione

788 °F

contiene

p-tert-butylcatechol as inhibitor

Limite di esplosione

12 %

P. eboll.

−4.5 °C (lit.)

Punto di fusione

−109 °C (lit.)

Solubilità

water: soluble 0.5 g/L at 20 °C

Densità

0.62 g/mL at 20 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

C=CC=C

InChI

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

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Descrizione generale

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.

Applicazioni

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.

Azioni biochim/fisiol

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.

Confezionamento

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:

Note legali

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

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Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

2A - Gases

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

-104.8 °F - closed cup

Punto d’infiammabilità (°C)

-76 °C - closed cup

Dispositivi di protezione individuale

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


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Isoprene 99%, contains <1000 ppm p-tert-butylcatechol as inhibitor

Sigma-Aldrich

I19551

Isoprene

Selective catalytic hydrodimerization of 1, 3-butadiene by palladium compounds dissolved in ionic liquids.
Dullius JEL, et al.
Organometallics, 17(5), 815-819 (1998)
Useful diene for the Diels-Alder reaction.
Danishefsky S and Kitahara T.
Journal of the American Chemical Society, 96(25), 7807-7808 (1974)
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
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)

Articoli

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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