Fortfahren mit
86320
Weinsteinsäure
≥97.0%
Synonym(e):
Hydroxymalonsäure
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 50 g | Warenkorb auf Verfügbarkeit prüfen | € 497,00 |
Über diesen Artikel
Lineare Formel:
HOCH(COOH)2
CAS-Nummer:
Molekulargewicht:
120.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-301-1
Beilstein/REAXYS Number:
1209791
MDL number:
Assay:
≥97.0%
Form:
powder
Technischer Dienst
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Unterstützung erhaltenassay
≥97.0%
form
powder
mp
158-160 °C (dec.) (lit.)
functional group
carboxylic acid, hydroxyl
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
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).
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Dieser Artikel | |||
|---|---|---|---|
| assay ≥97.0% | assay ≥97.0% | assay ≥95.0% (HPLC), ≥97.0% (T) | assay ≥97.0% |
| form powder | form powder or crystals | form powder | form solid |
| mp 158-160 °C (dec.) (lit.) | mp 45-50 °C | mp - | mp 30 °C (lit.) |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. - |
| functional group carboxylic acid, hydroxyl | functional group carboxylic acid, hydroxyl | functional group - | functional group - |
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 86320-10G | 04061833040874 |