Polyvinyl chloride

Base Information

• Chemical Name: Polyvinyl chloride
• CAS No.: 93050-82-9
• Molecular Formula: C₁₂H₁₆O₂
• Molecular Weight: 192.258
• Mol file: 93050-82-9.mol

Synonyms:PVC

Chemical Property of Polyvinyl chloride

Chemical Property:

• Vapor Pressure: 2580mmHg at 25°C
• Refractive Index: 1.383
• Density: 0.918g/cm³

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s): R36/37/38:
• Hazard Codes: Xi:Irritant
• Statements: R36/37/38:
• Safety Statements: S26:; S36/37:

MSDS Files:

Useful:

Technology Process of Polyvinyl chloride

There total 8 articles about Polyvinyl chloride 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: 94.0%

cycl-isopropylidene malonate (2033-24-1) + carvacrol (499-75-2) → carvacryl acetate (6380-28-5)

Guidance literature:

With triethylamine; In toluene; for 12h; Inert atmosphere; Reflux;

DOI:10.1039/d0gc03731a

Reference yield: 94.0%

carvacrol (499-75-2) + acetyl chloride (75-36-5) → carvacryl acetate (6380-28-5)

Guidance literature:

carvacrol; With sodium hydroxide; Amberlyst A₂₆;

acetyl chloride; In acetone; at 20 ℃; for 0.166667h; Further stages.;

DOI:10.1080/00397910701354608

Reference yield: 90.0%

carvacrol (499-75-2) + acetic anhydride (108-24-7) → carvacryl acetate (6380-28-5)

Guidance literature:

With silica-coated ferrite nanoparticles supported with montmorillonite-K₁₀; at 20 ℃; for 0.25h;

DOI:10.1039/d1ra02222a

upstream raw materials:

acetic anhydride

carvacrol

acetyl chloride

acetic acid

Refernces

• 1、 Schreiner, Linda,Bauer, Johannes,Ortner, Eva,Buettner, Andrea. "Structure-Odor Activity Studies on Derivatives of Aromatic and Oxygenated Monoterpenoids Synthesized by Modifying p-Cymene". supporting information. p. 834 - 842. Retrieved 2020/03/30.
• 2、 Ghosh, Santanu,Purkait, Anisha,Jana, Chandan K.. "Environmentally benign decarboxylative: N-, O-, and S-Acetylations and acylations". supporting information. p. 8721 - 8727. Retrieved 2020/12/30.