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2,3,5-Tricarboxycyclopentane-1-acetic acid is a tricarboxylic acid with a molecular formula C9H10O8, featuring a cyclopentane ring and an acetic acid functional group. 2,3,5-Tricarboxycyclopentane-1-acetic acid is known for its ability to form stable complexes with metal ions, making it a versatile agent in various industrial applications.

24434-90-0

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24434-90-0 Usage

Uses

Used in Water Treatment:
2,3,5-Tricarboxycyclopentane-1-acetic acid is used as a chelating agent for the removal of metal ions from water. Its complexing ability with metal ions helps in purifying water and preventing the buildup of metal deposits that can cause corrosion and other issues.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,3,5-Tricarboxycyclopentane-1-acetic acid is used as a complexing agent to facilitate reactions involving metal catalysts. Its ability to form stable complexes with metal ions aids in controlling reaction rates and improving the efficiency of chemical processes.
Used in Pharmaceutical Manufacturing:
2,3,5-Tricarboxycyclopentane-1-acetic acid is utilized as a chelating agent in the pharmaceutical industry to improve the solubility and stability of metal-containing drugs. Its complexing properties also help in the development of new drug formulations and the enhancement of drug delivery systems.
Used in Industrial Applications:
2,3,5-Tricarboxycyclopentane-1-acetic acid is employed as a versatile compound across various industries for its unique ability to form stable complexes with metal ions. This property is valuable in processes that require the management of metal ion concentrations, such as in the manufacturing of catalysts, dyes, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 24434-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24434-90:
(7*2)+(6*4)+(5*4)+(4*3)+(3*4)+(2*9)+(1*0)=100
100 % 10 = 0
So 24434-90-0 is a valid CAS Registry Number.

24434-90-0SDS

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 3-(carboxymethyl)cyclopentane-1,2,4-tricarboxylic acid

1.2 Other means of identification

Product number -
Other names <2,3,5-Tricarboxy-cyclopentyl>-essigsaeure

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:24434-90-0 SDS

24434-90-0Upstream product

24434-90-0Downstream Products

24434-90-0Relevant academic research and scientific papers

Preparation method of 3-carboxymethyl-1,2,4-cyclopentanetricarboxylic acid-1,4:2,3-dianhydride

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Paragraph 0018; 0020; 0022; 0024; 0026; 0028; 0030; 0032;, (2019/04/04)

The invention discloses a preparation method of 3-carboxymethyl-1,2,4-cyclopentanetricarboxylic acid-1,4:2,3-dianhydride and belongs to the field of preparation methods of fine chemicals. The main technical scheme is that dicyclopentadiene is taken as a starting material and subjected to oxidation reaction with ozone and hydrogen peroxide sequentially, intermediate product 2,3,5-tricarboxylic acidcyclopentane acetic acid is obtained, finally, acetic anhydride is taken as a dehydrating agent, and dehydration ring closing is performed for synthesizing the target product 3-carboxymethyl-1,2,4-cyclopentanetricarboxylic acid-1,4:2,3-dianhydride. The method in the scheme has the advantages of being mild in reaction condition, safe to operate, high in product purity and yield, pollution-free andthe like, and is suitable for large-scale industrial production.

A 2, 3, 5-three carboxyl cyclopentyl process for the preparation of acetic acid

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Paragraph 0059; 0060, (2017/09/19)

The invention discloses a method for preparing 2,3,5-tricarboxyl cyclopentylacetic acid. The method comprises the following steps: step 1, dissolving dicyclopentadiene in a mixed solvent of tetrahydrofuran and water; step 2, adding osmium tetroxide in a catalytic amount; step 3, adding sodium periodate; step 4, stirring for a certain time; step 5, pouring the mixture into water, and filtering; step 6, adding solids into a mixed solvent of an organic solvent and water; step 7, stirring, adding hydrogen peroxide, slowly heating to a certain temperature, and adding hydrogen peroxide in batches; step 8, stirring for a certain time; and step 9, distilling to obtain transparent viscous fluid, wherein a weight ratio of tetrahydrofuran to water in the step 1 is 1:1-10:1, a weight ratio of the mixed solvent to dicyclopentadiene is 40:1-100:1, and a weight ratio of osmium tetroxide to dicyclopentadiene is 1:500. The method for preparing the 2,3,5-tricarboxyl cyclopentylacetic acid disclosed by the invention is high in reaction speed and high in product purity and is suitable for large-scale industrial production.

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