Propylene

Base Information

• Chemical Name: Propylene
• CAS No.: 115-07-1
• Deprecated CAS: 33004-01-2,676-63-1,122302-77-6,212326-26-6,24979-91-7,25133-92-0,114717-91-8,195329-59-0,654653-11-9,1202863-88-4,1848947-38-5,2360817-60-1,2583823-77-0,648894-34-2,676-63-1
• Molecular Formula: C3H6
• Molecular Weight: 42.0806
• Hs Code.: 2901220000
• European Community (EC) Number: 204-062-1
• ICSC Number: 0559
• UN Number: 1077
• UNII: AUG1H506LY
• DSSTox Substance ID: DTXSID5021205
• Nikkaji Number: J2.463E
• Wikipedia: Propene
• Wikidata: Q151324,Q82918530
• RXCUI: 1314239
• Metabolomics Workbench ID: 50356
• ChEMBL ID: CHEMBL117213
• Mol file: 115-07-1.mol

Synonyms:isopropylidene;propene;propylene

Chemical Property of Propylene

Chemical Property:

• Appearance/Colour: colorless gas with a faint petroleum like odor
• Melting Point: -185 °C(lit.)
• Refractive Index: 1.3567
• Boiling Point: -47.7 °C(lit.)
• Flash Point: -108 °C
• PSA: 0.00000
• Density: 0.575 g/cm³
• LogP: 1.19230
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 42.0469501914
• Heavy Atom Count: 3
• Complexity: 7.5
• Transport DOT Label: Flammable Gas

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s): F+
• Hazard Codes: F++:极易燃物质
• Statements: R12:极端易燃
• Safety Statements: S9:保持容器在一个有良好通风放的场所‖S16

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Toxic Gases & Vapors -> Simple Asphyxiants
• Canonical SMILES: CC=C
• Inhalation Risk: On loss of containment this substance can cause suffocation by lowering the oxygen content of the air in confined areas.
• Effects of Short Term Exposure: Rapid evaporation of the liquid may cause frostbite. The substance may cause effects on the central nervous system. Exposure could cause lowering of consciousness.

Technology Process of Propylene

There total 4 articles about Propylene 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:

allyl iodid (556-56-9) → allyl radical (115-07-1,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4)

Guidance literature:

at 850 ℃;

Reference yield:

diallyl disulphide (2179-57-9) → allyl radical (115-07-1,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4)

Guidance literature:

at 750 ℃;

Reference yield:

diallyl oxalate (615-99-6) → allyl radical (115-07-1,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4)

Guidance literature:

at 850 ℃;

upstream raw materials:

allyl iodid

diallyl disulphide

diallyl oxalate

1,5-Hexadien

Refernces