1,3-Butadiene is a chemical made from the processing of petroleum. It is the 36th highest volume chemical produced in the United States. It is a colorless gas with a mild gasoline-like odor. About 75% of the manufactured 1,3-butadiene is used to make synthetic rubber.

1,3-Butadiene (/ ˌbjuːtəˈdaɪiːn / ⓘ) [8] is the organic compound with the formula CH 2 =CH-CH=CH 2. It is a colorless gas that is easily condensed to a liquid. It is important industrially as a precursor to synthetic rubber. [9] . The molecule can be viewed as the union of two vinyl groups. It is the simplest conjugated diene.

Structural Formula. C 4 H 6. 1,3-butadiene

Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Permanent link for this species. Use this link for bookmarking this species for future reference.

1,3-BUTADIENE contains total 9 bond (s); 3 non-H bond (s), 2 multiple bond (s), 1 rotatable bond (s), and 2 double bond (s). Learn more about chemical structure at Mol-Instincts.

Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Permanent link for this species. Use this link for bookmarking this species for future reference.

ChemSpider record containing structure, synonyms, properties, vendors and database links for butadiene, 106-99-0, 605258, KAKZBPTYRLMSJV-UHFFFAOYSA-N

This page explores the application of Hückel theory and molecular orbital theory to 1,3-butadiene, focusing on its molecular structure, electronic properties, and delocalization energy. The …

The 1,3-butadiene is the simplest member of the series of conjugated dienes, which contain the structure C=C―C=C, the C being carbon. The wide variety of chemical reactions peculiar to this system makes butadiene important in chemical synthesis.

1 3 butadiene structure is in its most stable form only when a molecule of 1 3 butadiene exists in s-trans conformation. In this conformational structure, the molecule is planar and the two pairs of the double bonds are facing the opposite directions.