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1,3,5-Pentanetricarboxylic acid, also known as trimellitic acid, is a white crystalline solid with the molecular formula C9H6O6. It is insoluble in water and has a high melting point. This chemical compound serves as a crucial precursor in the production of various polymers and resins, making it an essential component in the manufacturing of a wide range of industrial products.

6940-58-5

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6940-58-5 Usage

Uses

Used in Polymer and Resin Production:
1,3,5-Pentanetricarboxylic acid is used as a precursor for the production of polyester resins and alkyd resins. Its presence in these materials contributes to their structural integrity and performance characteristics.
Used in Coating and Adhesive Manufacturing:
1,3,5-Pentanetricarboxylic acid functions as a crosslinking agent in the production of coatings and adhesives. This role enhances the durability and bonding capabilities of these products, making them more effective for various applications.
Used in Plasticizer Production:
1,3,5-Pentanetricarboxylic acid is utilized in the creation of plasticizers, which are additives that increase the flexibility and workability of materials such as plastics and rubbers.
Used in Corrosion Inhibition:
1,3,5-Pentanetricarboxylic acid also serves as a corrosion inhibitor, protecting materials from the damaging effects of corrosion and extending their service life in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6940-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6940-58:
(6*6)+(5*9)+(4*4)+(3*0)+(2*5)+(1*8)=115
115 % 10 = 5
So 6940-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O6/c9-6(10)3-1-5(8(13)14)2-4-7(11)12/h5H,1-4H2,(H,9,10)(H,11,12)(H,13,14)

6940-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Pentanetricarboxylic Acid

1.2 Other means of identification

Product number -
Other names pentane-1,3,5-tricarboxylic acid

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:6940-58-5 SDS

6940-58-5Relevant academic research and scientific papers

Synthesis and conformation studies of a dodecaazanonacyclotetratetracontane

Suissa, M. Rachel,Romming, Christian,Dale, Johannes

, p. 3055 - 3065 (2007/10/03)

Compound 3 was prepared by self-assembly of 1,3,5-pentanetriamine and aqueous formaldehyde in quantitative yield (Figure 1). This molecule can exist in four well-defined diamond-lattice conformations of symmetries D(2d), S4, C(2v) and D(2d). Low-temperature 13C NMR spectroscopy indicates the existence of three main conformers; their relative populations depend on the solvent used. An extra set of low- intensity lines is also observed. A conformation interconversion scheme is proposed; it involves two additional less populated quasi-diamond-lattice intermediates derived from a helix compressed along its axis. One of these is trapped as a 1:2 clathrate with 1,4-dioxane; its crystal structure is reported.

Stabilized acid anhydrides

-

, (2008/06/13)

Acid anhydrides such as maleic anhydride are stabilized against the deteriorative effects of heat by addition thereto of an inorganic boron-oxygen compound typified by boric acid, boric anhydride, tributly borate, or borax.

Synthetic Studies in Carbocyclic Systems : Part I - A new Synthesis of Nopinone

Murthi, G. S. S.,Mazumder, Alok

, p. 339 - 340 (2007/10/02)

Base-induced intramolecular nucleophilic displacement of the tosyloxy group of 4-isopropyl-7-tosyloxycyclohexanone affords nopinone , identical with an authentic specimen.

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