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86320

Sigma-Aldrich

Tartronic acid

≥97.0%

Synonyme(s) :

Hydroxymalonic acid, Hydroxypropanedioic acid

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About This Item

Formule linéaire :
HOCH(COOH)2
Numéro CAS:
80-69-3
Poids moléculaire :
120.06
Numéro Beilstein :
1209791
Numéro CE :
201-301-1
Numéro MDL:
MFCD00004237
Code UNSPSC :
12352100
ID de substance PubChem :
329769456
Nomenclature NACRES :
NA.22

Pureté

≥97.0%

Forme

powder

Pf

158-160 °C (dec.) (lit.)

Groupe fonctionnel

carboxylic acid
hydroxyl

Température de stockage

2-8°C

Chaîne SMILES 

OC(C(O)=O)C(O)=O

InChI

1S/C3H4O5/c4-1(2(5)6)3(7)8/h1,4H,(H,5,6)(H,7,8)

Clé InChI

ROBFUDYVXSDBQM-UHFFFAOYSA-N

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Application


  • Polymer synthesis for enhanced thermal conductivity: Tartronic acid is used to exploit enzyme reactions in polymer synthesis, significantly increasing the thermal conductivity of materials, which is pivotal in manufacturing and material science applications (Nan et al., 2023).

  • Advances in green chemical treatments: This acid plays a role in the electro-oxidation pathways for treating glycerol waste, contributing to sustainable chemical processes and green chemistry applications, which are essential for reducing environmental impact (Cheng et al., 2021).

  • Development in biodiesel by-products treatment: Tartronic acid is also involved in kinetic studies for the electrochemical conversion of glycerol, a by-product of biodiesel production, highlighting its role in renewable energy and waste valorization (Pérès et al., 2020).

  • Base-free oxidation reactions: It aids in the development of base-free conditions for glycerol to glyceraldehyde oxidation reactions over platinum-based catalysts, offering advancements in catalysis and organic synthesis processes (Capron et al., 2019).

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
WXBF2988V
WXBF0336V
WXBD7848V
WXBD5590V
WXBD3810V

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A Shah et al.
Bioorganic & medicinal chemistry, 5(2), 323-334 (1997-02-01)
A new, aromatic analogue of the EPSP synthase enzyme reaction intermediate 1 has been identified, which contains a 3-hydroxymalonate moiety in place of the usual 3-phosphate group. This simplified inhibitor was readily prepared in five steps from ethyl 3,4-dihydroxybenzoate. The
S H Park et al.
Biochemistry, 23(23), 5446-5453 (1984-11-06)
Measurement of the initial rate of the malic enzyme reaction varying the concentration of NAD at several different fixed levels of Mg2+ (0.25-1.0 mM) and a single malate concentration gave a pattern which intersects to the left of the ordinate.
G Gutierrez et al.
Journal of applied physiology (Bethesda, Md. : 1985), 76(6), 2735-2741 (1994-06-01)
Lactate uptake by skeletal muscle occurs under diverse conditions, including hypoxia and electrical stimulation. A possible metabolic fate of lactate in resting muscle is its conversion to pyruvate followed by carboxylation to malate in the cytosolic malic reaction. To test
A Cortés et al.
The Biochemical journal, 357(Pt 1), 263-268 (2001-06-21)
The concentration of an inhibitor that decreases the rate of an enzyme-catalysed reaction by 50%, symbolized i(0.5), is often used in pharmacological studies to characterize inhibitors. It can be estimated from the common inhibition plots used in biochemistry by means
A dynamic kinetic asymmetric transformation in the alpha-hydroxylation of racemic malonates and its application to biologically active molecules.
Dhande Sudhakar Reddy et al.
Angewandte Chemie (International ed. in English), 48(4), 803-806 (2008-12-23)
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