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Merck
CN

86320

Sigma-Aldrich

亚酒石酸

≥97.0%

别名:

丙醇二酸, 羟基丙二酸

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About This Item

线性分子式:
HOCH(COOH)2
CAS号:
分子量:
120.06
Beilstein:
1209791
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

≥97.0%

表单

powder

mp

158-160 °C (dec.) (lit.)

官能团

carboxylic acid
hydroxyl

储存温度

2-8°C

SMILES字符串

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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应用


  • 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).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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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)
Formation of 2-keto-D-gluconic acid, 5-keto-D-gluconic acid, and tartronic acid by Acetobacter species.
D KULKA et al.
Nature, 167(4257), 905-906 (1951-06-02)
Christopher D Evans et al.
The Journal of chemical physics, 152(13), 134705-134705 (2020-04-10)
The oxidation of glycerol under alkaline conditions in the presence of a heterogeneous catalyst can be tailored to the formation of lactic acid, an important commodity chemical. Despite recent advances in this area, the mechanism for its formation is still
J K Hiltunen et al.
Biochimica et biophysica acta, 678(1), 115-121 (1981-11-18)
The mechanism of depletion of tricarboxylic acid cycle intermediates by isolated rat heart mitochondria was studied using hydroxymalonate (an inhibitor of malic enzymes) and mercaptopicolinate (an inhibitor of phosphoenolpyruvate carboxykinase) as tools. Hydroxymalonate inhibited the respiration rate of isolated mitochondria
Xin'e Shi et al.
Life sciences, 258, 118240-118240 (2020-08-12)
As a dicarboxylic acid with the structural formula HOOCCH (OH) COOH, tartronic acid is considered as an inhibitor of the transformation of carbohydrates into fat under fat-deficient diet conditions. However, the effect of tartronic acid on lipogenesis under high-fat diet

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