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(2R)-2-hydroxybutane-1,2,4-tricarboxylic acid, also known as HBT, is a tricarboxylic acid compound with optical activity, characterized by the (2R) stereochemistry where the hydroxy group is positioned on the second carbon of the butane chain. HBT is naturally present in certain bacteria and fungi and plays a pivotal role in the microbial breakdown of aromatic compounds. Its potential as a chelating agent for metal ions has positioned it as a candidate for various environmental and industrial applications, with its distinctive structure and properties inviting further research and exploration for novel uses.

3562-74-1

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3562-74-1 Usage

Uses

Used in Environmental Applications:
HBT is utilized as a chelating agent for metal ions, which is instrumental in environmental remediation processes. Its ability to bind with metal ions aids in the detoxification of contaminated sites and the management of heavy metal pollution.
Used in Industrial Applications:
In industrial settings, HBT serves as a versatile compound for the development of new processes and products. Its chelating properties can be harnessed to improve various industrial processes, such as in the manufacturing of detergents, where it can help to stabilize and enhance the performance of cleaning agents.
Used in Microbial Degradation:
HBT is employed in the biodegradation of aromatic compounds, a process that is crucial for the natural breakdown of pollutants and the recycling of nutrients in ecosystems. Its role as an intermediate in this process highlights its importance in environmental sustainability and bioremediation strategies.
Used in Research and Development:
HBT's unique structure and properties make it an intriguing compound for scientific research and development. It is used as a subject of study to explore new chemical reactions, potential pharmaceutical applications, and its behavior in various chemical and biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 3562-74-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3562-74:
(6*3)+(5*5)+(4*6)+(3*2)+(2*7)+(1*4)=91
91 % 10 = 1
So 3562-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O7/c8-4(9)1-2-7(14,6(12)13)3-5(10)11/h14H,1-3H2,(H,8,9)(H,10,11)(H,12,13)/t7-/m1/s1

3562-74-1SDS

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 homocitric acid

1.2 Other means of identification

Product number -
Other names 2-hydroxyl n-butyl 1,2,4-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:3562-74-1 SDS

3562-74-1Downstream Products

3562-74-1Relevant academic research and scientific papers

Cyanide as a primordial reductant enables a protometabolic reductive glyoxylate pathway

Krishnamurthy, Ramanarayanan,Pulletikurti, Sunil,Yadav, Mahipal,Yerabolu, Jayasudhan R.

, p. 170 - 178 (2022/02/11)

Investigation of prebiotic metabolic pathways is predominantly based on abiotically replicating the reductive citric acid cycle. While attractive from a parsimony point of view, attempts using metal/mineral-mediated reductions have produced complex mixtures with inefficient and uncontrolled reactions. Here we show that cyanide acts as a mild and efficient reducing agent mediating abiotic transformations of tricarboxylic acid intermediates and derivatives. The hydrolysis of the cyanide adducts followed by their decarboxylation enables the reduction of oxaloacetate to malate and of fumarate to succinate, whereas pyruvate and α-ketoglutarate themselves are not reduced. In the presence of glyoxylate, malonate and malononitrile, alternative pathways emerge that bypass the challenging reductive carboxylation steps to produce metabolic intermediates and compounds found in meteorites. These results suggest a simpler prebiotic forerunner of today’s metabolism, involving a reductive glyoxylate pathway without oxaloacetate and α-ketoglutarate—implying that the extant metabolic reductive carboxylation chemistries are an evolutionary invention mediated by complex metalloproteins. [Figure not available: see fulltext.].

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