POLYBUTADIENE DIACRYLATE

Base Information

• Chemical Name: POLYBUTADIENE DIACRYLATE
• CAS No.: 9003-17-2
• Molecular Formula: (C4H6)x
• Molecular Weight: 54.09044
• Hs Code.: 39029090
• Mol file: 9003-17-2.mol

Synonyms:1,3-Butadiene,homopolymer;1,3-Butadiene, polymers;Atactic butadiene polymer;Butadiene homopolymer;Butadiene resin;Nisso BN 1000;

Chemical Property of POLYBUTADIENE DIACRYLATE

Chemical Property:

• Melting Point: −6 °C
• Refractive Index: n20/D 1.524
• Flash Point: 113 °C
• PSA: 0.00000
• Density: 0.9 g/mL at 25 °C(lit.)
• LogP: 1.47780
• Storage Temp.: Store at R.T.
• Solubility.: aliphatic hydrocarbons: soluble

Purity/Quality:

100% ^*data from raw suppliers

Polybutadiene average Mw ~200,000 ^*data from reagent suppliers

Safty Information:

• Safety Statements: S24/25:Avoid contact with skin and eyes.

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Component of water soluble binders and electrical encapsulants. Co-reactant for air curing coatings. PB-cis can be polymerized with styrene for the formation of high impact polystyrene (HIPS). It may also be used as a toughening agent for acrylonitrile butadiene rubber (ABS) based resins.

Technology Process of POLYBUTADIENE DIACRYLATE

There total 991 articles about POLYBUTADIENE DIACRYLATE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 0.3%

exo-vinylnorbornene (3048-64-4,23890-32-6,25093-48-5,117110-17-5,117110-18-6,142037-50-1) + endo-vinylnorbornene (3048-64-4,23890-32-6,25093-48-5,117110-17-5,117110-18-6,142037-50-1) → 4-ethenylcyclohexene (100-40-3) + bicyclo[4.3.0]nona-3,7-diene (3048-65-5) + 5-vinyl-2-norbornene (3048-64-4,23890-32-6,25093-48-5,117110-17-5,117110-18-6,142037-50-1) + dicyclopentadiene (77-73-6,933-60-8,1755-01-7,13257-74-4,25850-35-5,57429-84-2,109428-68-4,25038-78-2) + cyclopenta-1,3-diene (542-92-7,25568-84-7,7313-32-8) + buta-1,3-diene (106-99-0,130983-70-9,29406-96-0,9003-17-2)

Guidance literature:

at 150 ℃; for 69.6333h; Product distribution / selectivity; Pyrolysis;

Reference yield:

1-penten (109-67-1) → 2-pentyloxirane (1003-14-1) + Z-piperylene (1574-41-0,17410-45-6,25212-15-1,64940-84-7) + 1-methylbuta-1,3-diene (2004-70-8,17410-45-6,25212-15-1,64940-84-7) + propene (187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4) + ethene (74-85-1) + buta-1,3-diene (106-99-0,130983-70-9,29406-96-0,9003-17-2)

Guidance literature:

With (per)acetylperoxyboric acid; hydrogen; oxygen; at 480 ℃; Mechanism;

DOI:10.1039/f19807602396

Reference yield:

trans-1,3-Divinylcyclobutan (77614-67-6) → 4-ethenylcyclohexene (100-40-3) + cis-1,3-divinylcyclobutane (77614-53-0) + buta-1,3-diene (106-99-0,130983-70-9,29406-96-0,9003-17-2)

Guidance literature:

at 325 ℃; for 1.1h; under 30 Torr; Product distribution; pyrolysis;

upstream raw materials:

oxirane

ethanol

ethene

tetrahydrofuran

Downstream raw materials:

2-(3-cyclohexenyl)pyridine

cis-7-thiabicyclo<4.3.0>non-3-ene 7,7-dioxide

cis-2-phenyl-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione

1-methyl-cyclohex-3-enecarboxylic acid ethyl ester

Refernces

• 1、 Kiyokawa, Takayasu,Ikenaga, Naoki. "Oxidative dehydrogenation of n-butene to buta-1,3-diene with novel iron oxide-based catalyst: Effect of iron oxide crystalline structure". . . Retrieved 2021/04/19.
• 2、 -. "SUPPORTED TANTALUM CATALYST FOR THE PRODUCTION OF 1,3-BUTADIENE". Page/Page column 14-17. . Retrieved 2021/04/03.