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585-84-2

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585-84-2 Usage

Chemical Properties

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Uses

Different sources of media describe the Uses of 585-84-2 differently. You can refer to the following data:
1. cis-Aconitic Acid is the cis-isomer of Aconitic Acid. The conjugate base of cis-Aconitic Acid is an intermediate in the isomerization of citrate and isocitrate in the citric acid cycle.
2. cis-Aconitic acid is used as an intermediate in the production of substances pharmaceuticals. It is widely used in chemical research and as reagent. It acts as a cis-isomer of aconitic acid.
3. cis-Aconitic acid can be used as a standard for the determination of organic acids in plant tissues.

Definition

ChEBI: The cis-isomer of aconitic acid.

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Purification Methods

Crystallise the cis-acid from water by cooling (solubility is 1g in 2mL of water at 25o). Dry it in a vacuum desiccator. [Beilstein 2 IV 2405.]

Check Digit Verification of cas no

The CAS Registry Mumber 585-84-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 585-84:
(5*5)+(4*8)+(3*5)+(2*8)+(1*4)=92
92 % 10 = 2
So 585-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O6/c7-4(8)1-3(6(11)12)2-5(9)10/h1H,2H2,(H,7,8)(H,9,10)(H,11,12)/b3-1-

585-84-2 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (A16010)  cis-Aconitic acid, tech. 90%   

  • 585-84-2

  • 1g

  • 453.0CNY

  • Detail
  • Alfa Aesar

  • (A16010)  cis-Aconitic acid, tech. 90%   

  • 585-84-2

  • 5g

  • 1522.0CNY

  • Detail
  • Alfa Aesar

  • (A16010)  cis-Aconitic acid, tech. 90%   

  • 585-84-2

  • 25g

  • 5191.0CNY

  • Detail

585-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Propene-1,2,3-tricarboxylic acid, cis-

1.2 Other means of identification

Product number -
Other names cis-Citridic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:585-84-2 SDS

585-84-2Relevant articles and documents

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.].

Reaction of maleic anhydride with active methylene or methine containing compounds

-

, (2008/06/13)

Novel polyfunctional compounds and a process for their preparation are disclosed. These compounds and their alkali metal salts are useful metal sequestrants and/or detergent builders. Selected compounds are also intermediates useful in the syntheses of aconitic acid as well as isocitric and alloisocitric acids and their lactones. The novel polyfunctional compounds are obtained from the reaction of maleic anhydride with selected active methylene or methine containing compounds.

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