Dipropyl succinate

Base Information

• Chemical Name: Dipropyl succinate
• CAS No.: 925-15-5
• Molecular Formula: C10H18 O4
• Molecular Weight: 202.251
• Hs Code.: 2917190090
• European Community (EC) Number: 213-114-2
• DSSTox Substance ID: DTXSID80239018
• Nikkaji Number: J43.443D
• Wikidata: Q63399661
• Mol file: 925-15-5.mol

Synonyms:Dipropyl succinate;925-15-5;Di-n-propyl succinate;dipropyl butanedioate;SUCCINIC ACID, DIPROPYL ESTER;Butanedioic acid, dipropyl ester;Dipropylester kyseliny jantarove;EINECS 213-114-2;BRN 1779461;Dipropylester kyseliny jantarove [Czech];AI3-05512;Succinic acid di-n-propyl ester;n-Propyl succinate;MFCD00015213;1,4-dipropyl butanedioate;Succinic acid dipropyl ester;SCHEMBL20589;butanedioic acid dipropyl ester;DTXSID80239018;Di-N-Propyl succinate AldrichCPR;Di-N-Propyl succinate, AldrichCPR;AKOS015839519;AS-57077;LS-147435;CS-0368241;FT-0625199;A860058;J-520389;Q63399661

Chemical Property of Dipropyl succinate

Chemical Property:

• Appearance/Colour: Liquid
• Vapor Pressure: 0.0212mmHg at 25°C
• Melting Point: -10.4ºC
• Refractive Index: 1.4250 (estimate)
• Boiling Point: 250-252°C
• Flash Point: 111.4 °C
• PSA: 52.60000
• Density: 1 g/cm³
• LogP: 1.67300
• Storage Temp.: 2-8°C
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 9
• Exact Mass: 202.12050905
• Heavy Atom Count: 14
• Complexity: 157

Purity/Quality:

99% ^*data from raw suppliers

DipropylSuccinate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 52/53

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCOC(=O)CCC(=O)OCCC
• Uses: Alkyl succinates have been used as ashless dispersants and detergent additives for lubricating oils.

Technology Process of Dipropyl succinate

There total 7 articles about Dipropyl succinate 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: 97.0%

propan-1-ol (71-23-8) + succinic acid (110-15-6) → dipropyl succinate (925-15-5)

Guidance literature:

With alumina methanesulfonic acid; at 80 ℃; for 0.133333h; Microwave irradiation;

DOI:10.1080/00397911.2013.875210

Reference yield: 80.5%

propan-1-ol (71-23-8) + n-propyl levulinate (645-67-0) → dipropyl oxalate (615-98-5) + dipropyl succinate (925-15-5)

Guidance literature:

n-propyl levulinate; With manganese(II) sulfate; acetic acid; at 100 ℃; for 10h; under 4500.45 Torr;

propan-1-ol; With sulfuric acid; for 6h;

Reference yield:

propan-1-ol (71-23-8) + Cellobiose (13360-52-6) → dipropyl succinate (925-15-5)

Guidance literature:

With oxygen; molybdenum trioxide; at 150 ℃; for 6h; under 3750.38 Torr;

upstream raw materials:

propan-1-ol

succinic acid

di-n-propyl phosphonate

diallyl maleate

Downstream raw materials:

di-n-propyl 1,4-cyclohexanedicarboxylate

3,6-bis-(4-(2-ethylhexyloxy)phenyl)-2,5-dihydropyrrolyl[3,4-c]pyrrole-1,4-dione

2,5-dipropylformate 1,4-cyclohexanedione

Refernces

• 1、 -. "Method for preparing disuccinate". Paragraph 0021-0022. . Retrieved 2019/01/07.
• 2、 Fabian, Lucas,Gomez, Matias,Kuran, Juan A. Caturelli,Moltrasio, Graciela,Moglioni, Albertina. "Efficient microwave-assisted esterification reaction employing methanesulfonic acid supported on alumina as catalyst". . p. 2386 - 2392. Retrieved 2014/07/22.