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Tetrasodium benzene-1,2,4,5-tetracarboxylate, also known as sodium benzene-1,2,4,5-tetracarboxylate or sodium pyromellitate, is a chemical compound with the formula C10H2O8Na4. It is a sodium salt derived from benzene-1,2,4,5-tetracarboxylic acid, featuring a benzene ring with four carboxyl groups attached to it. tetrasodium benzene-1,2,4,5-tetracarboxylate is widely used in various applications, including as a chelating agent, a sequestrant, and a stabilizer in industrial processes, particularly in the production of detergents, water treatment chemicals, and metal cleaning solutions. Its ability to form stable complexes with metal ions makes it an effective agent for preventing scale formation and corrosion in water systems. Additionally, it is used in the synthesis of other organic compounds and as a component in some types of batteries.

148-04-9

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148-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148-04-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148-04:
(5*1)+(4*4)+(3*8)+(2*0)+(1*4)=49
49 % 10 = 9
So 148-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H6O8.4Na/c11-7(12)3-1-4(8(13)14)6(10(17)18)2-5(3)9(15)16;;;;/h1-2H,(H,11,12)(H,13,14)(H,15,16)(H,17,18);;;;/q;4*+1/p-4

148-04-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tetrasodium,benzene-1,2,4,5-tetracarboxylate

1.2 Other means of identification

Product number -
Other names EINECS 205-709-0

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:148-04-9 SDS

148-04-9Upstream product

148-04-9Relevant academic research and scientific papers

Exploration of a calcium-organic framework as an anode material for sodium-ion batteries

Zhang, Yan,Niu, Yubin,Wang, Min-Qiang,Yang, Jingang,Lu, Shiyu,Han, Jin,Bao, Shu-Juan,Xu, Maowen

, p. 9969 - 9971 (2016)

In this communication, we designed and synthesized a novel calcium-organic framework and presented it as an anode material for sodium-ion batteries. The results show that it delivers a reversible capacity of higher than 140 mA h g-1 even after 300 cycles. The remarkable performance is attributed to the high structural stability and extremely low solubility of the calcium-organic framework in electrolytes.

Colorless polyimides derived from 1S,2S,4R,5R-cyclohexanetetracarboxylic dianhydride, self-orientation behavior during solution casting, and their optoelectronic applications

Hasegawa, Masatoshi,Fujii, Mari,Ishii, Junichi,Yamaguchi, Shinya,Takezawa, Eiichiro,Kagayama, Takashi,Ishikawa, Atsushi

, p. 4693 - 4708 (2014/11/08)

A novel cycloaliphatic monomer for polyimides (PI), 1S,2S,4R,5R- cyclohexanetetracarboxylic dianhydride (H′-PMDA) is proposed in this work. H′-PMDA shows high polymerizability with various diamines in contrast to its isomer, i.e., conventional hydrogenated pyromellitic dianhydride (H-PMDA) and leads to highly flexible and colorless PI films with very high T g's. In particular, the combinations with rigid structures of diamines give rise to PIs with significantly decreased coefficients of thermal expansion (CTE) owing to high extents of in-plane chain orientation induced by thermal imidization, whereas the H-PMDA-based counterparts do not. The decreased CTE reflects structural rigidity/linearity of the H′-PMDA-based diimide units as supported by liquid crystallinity observed in the corresponding model compound. Solution casting of a chemically imidized PI derived from H′-PMDA and 2,2′-bis(trifluoromethyl)benzidine (TFMB) results in a lower CTE than that of the thermally imidized counterpart, suggesting the presence of a self-orientation phenomenon during solvent evaporation. The mechanism is proposed in this work. H′-PMDA/TFMB and its copolymer systems can be useful as plastic substrates in image display devices and/or novel coating-type optical compensation films.

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