86320
Tartronic acid
≥97.0%
Synonym(s):
Hydroxymalonic acid, Hydroxypropanedioic acid
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About This Item
Linear Formula:
HOCH(COOH)2
CAS Number:
Molecular Weight:
120.06
Beilstein:
1209791
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥97.0%
form
powder
mp
158-160 °C (dec.) (lit.)
storage temp.
2-8°C
SMILES string
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)
InChI key
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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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