1,4-Benzenedicarboxylic acid, sodium salt (1:)

Base Information

• Chemical Name: 1,4-Benzenedicarboxylic acid, sodium salt (1:)
• CAS No.: 10028-70-3
• Molecular Formula: C8H6 O4 . 2 Na
• Molecular Weight: 210.097
• Hs Code.: 2917369000
• Mol file: 10028-70-3.mol

Synonyms:1,4-Benzenedicarboxylic acid, sodium salt (1:);disodium tereph-thalate;SCHEMBL104074

Chemical Property of 1,4-Benzenedicarboxylic acid, sodium salt (1:)

Chemical Property:

• Vapor Pressure: 7.35E-07mmHg at 25°C
• Boiling Point: 392.4°Cat760mmHg
• Flash Point: 205.3°C
• PSA: 80.26000
• Density: g/cm³
• LogP: -1.58640
• Water Solubility.: Soluble in water.
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 189.01637795
• Heavy Atom Count: 13
• Complexity: 169

Purity/Quality:

98%,99%, ^*data from raw suppliers

Disodium Terephthalate ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC(=CC=C1C(=O)O)C(=O)O.[Na]
• Uses: Disodium terephthalate and its various derivatives are synthesized via simple acid-base chemistry for anode materials in Na ion batteries. They show excellent electrochemical performance, including little capacity fading over 90 cycles, ideal redox potential, and excellent rate performance, making them promising candidates for Na ion batteries.

Technology Process of 1,4-Benzenedicarboxylic acid, sodium salt (1:)

There total 6 articles about 1,4-Benzenedicarboxylic acid, sodium salt (1:) 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: 98.0%

polyethylene terephthalate → disodium terephthalate (10028-70-3) + ethylene glycol (107-21-1)

Guidance literature:

With sodium hydroxide; In octanol; at 183 ℃; for 0.0833333h; Product distribution / selectivity;

Reference yield: 95.0%

terephthalic acid (100-21-0) → disodium terephthalate (10028-70-3)

Guidance literature:

With sodium hydroxide; In water;

DOI:10.1016/j.tet.2014.02.061

Reference yield: 48.0%

poly(ethylene terephthalate) → disodium terephthalate (10028-70-3) + ethylene glycol (107-21-1)

Guidance literature:

With sodium hydroxide; at 100 - 150 ℃; under 760.051 - 2250.23 Torr;

upstream raw materials:

Monomethyl terephthalate

terephthalic acid

Downstream raw materials:

p-dibenzyl benzenedicarboxylate

terephthalic acid

(μ-terephthalato)(ethylenediamine)diaquacopper(II)

Zn(1,4-benzenedicarboxylate)(H₂O)

Refernces

• 1、 Ma, Lingzhi,Yang, Tianfeng,Zhang, Zeyuan,Yin, Siping,Song, Zhongxiao,Shi, Wen,Chu, Dake,Zhang, Yanmin,Zhang, Mingming. "Cyanostilbene-based near-infrared emissive platinum(II) metallacycles for cancer theranostics". . p. 1942 - 1946. Retrieved 2019.
• 2、 Zhao, Hongyang,Wang, Jianwei,Zheng, Yuheng,Li, Ju,Han, Xiaogang,He, Gang,Du, Yaping. "Organic Thiocarboxylate Electrodes for a Room-Temperature Sodium-Ion Battery Delivering an Ultrahigh Capacity". . p. 15334 - 15338. Retrieved 2017.
• 3、 Narkhede, Nilesh,Uttam, Bhawna,Rao, Chebrolu Pulla. "Inorganic-organic covalent hybrid of polyoxometalate-calixarene: Synthesis, characterization and enzyme mimetic activity". . p. 337 - 342. Retrieved 2018.