Bis(2-ethylbutyl) phthalate

Base Information

• Chemical Name: Bis(2-ethylbutyl) phthalate
• CAS No.: 7299-89-0
• Molecular Formula: C20H30O4
• Molecular Weight: 334.456
• European Community (EC) Number: 230-741-7
• NSC Number: 15317
• UNII: Q298IR7BMM
• DSSTox Substance ID: DTXSID70223269
• Nikkaji Number: J104.841D
• Wikidata: Q27286915
• Mol file: 7299-89-0.mol

Synonyms:Bis(2-ethylbutyl) phthalate;7299-89-0;bis(2-ethylbutyl) benzene-1,2-dicarboxylate;Bis(2-ethyl-n-butyl) phthalate;Phthalic acid, bis(2-ethylbutyl) ester;1,2-Benzenedicarboxylic acid, bis(2-ethylbutyl) ester;Bis(2-ethylbutyl)phthalate;UNII-Q298IR7BMM;Q298IR7BMM;EINECS 230-741-7;NSC 15317;NSC-15317;AI3-04276;di-(2-ethylbutyl)phthalate;1, bis(2-ethylbutyl) ester;SCHEMBL420283;DTXSID70223269;NSC15317;Phthalic acid di(2-ethylbutyl) ester;phthalic acid bis-(2-ethyl-butyl) ester;AS-75848;D97205;Q27286915;BIS(2-ETHYLBUTYL) BENZENE-1,2-DICARBOXYLATE ESTER

Chemical Property of Bis(2-ethylbutyl) phthalate

Chemical Property:

• Vapor Pressure: 8.01E-05mmHg at 25°C
• Boiling Point: 341.5°Cat760mmHg
• Flash Point: 180°C
• PSA: 52.60000
• Density: 1.01g/cm³
• LogP: 4.87260
• Storage Temp.: Refrigerator
• Solubility.: Chloroform, Methanol
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 334.21440943
• Heavy Atom Count: 24
• Complexity: 336

Purity/Quality:

98% ^*data from raw suppliers

Bis(2-Ethylbutyl)Phthalate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CC
• Uses: Bis(2-Ethylbutyl) Phthalate, can be used in plastics manufacture and processing.

Technology Process of Bis(2-ethylbutyl) phthalate

There total 1 articles about Bis(2-ethylbutyl) phthalate 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:

phthalic anhydride (85-44-9) + 2-ethyl-1-butanol (97-95-0) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → 1,2-benzenedicarboxylic acid bis(2-ethylbutyl) ester (7299-89-0)

Guidance literature:

With sulfuric acid; unter Entfernen des entstehenden Wassers;

upstream raw materials:

phthalic anhydride

2-ethyl-1-butanol

benzene