Sodium malondialdehyde.
- CAS NO.：24382-04-5
- Empirical Formula: C3H3NaO2
- Molecular Weight: 94.04
- SAFETY DATA SHEET (SDS)
- Update Date: 2025-06-13 14:48:16
What is Sodium malondialdehyde.?
The Uses of Sodium malondialdehyde.
Biomarker for oxidative stress. Index of oxidative rancidity in foods.
General Description
Light yellow powder.
Air & Water Reactions
Water soluble.
Reactivity Profile
Sodium malondialdehyde. is an aldehyde. is an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. Sodium malondialdehyde. is sensitive to light and heat. Dilute aqueous solutions (1%) are stable when stored at -4° F in the dark for 7 days.
Fire Hazard
Flash point data for Sodium malondialdehyde. are not available; however, Sodium malondialdehyde. is probably combustible.
Properties of Sodium malondialdehyde.
| Melting point: | 246° (dec) |
| EPA Substance Registry System | Sodium malonaldehyde (24382-04-5) |
Safety information for Sodium malondialdehyde.
Computed Descriptors for Sodium malondialdehyde.
New Products
Levothyroxine Impurity-F Montelukast EP Impurity-D/Montelukast USP Related Compound C Atorvastatin FXA Impurity/Atorvastatin Cyclic 6-Hydroxy Impurity Sodium Salt Isosulfan blue Keto N-Oxide Impurity Ivermectin Impurity F N-Nitroso des Methyl Tramadol/N-Nitroso-N-Desmethyl-Tramadol DL-beta-(3-Bromophenyl)alanine Tetrabutylammonium perchlorate N,O-Dimethylhydroxylamine hydrochloride (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid 2-Amino-5-bromo-4-(trifluoromethyl)pyridine（RM for Indian lab) N,N CARBONYL DIIMIDAZOLE (R)-BoroLeu-(+)-Pinanediol-CF3COOH 1,4-bis(methylsulfonyl)butane 4-(5-amino-1-methyl-1h-benzoimidazol-2-yl)-butyric acid isopropyl ester. 5-Methyl-1,3-benzenediacetonitrile 4-Fluorothiophenol 1-methyl amino-2,4-dinitro benzene CSA (DL-10-Camphorsulfonic Acid) 2-Hydroxy-4-methylnicotinic acid 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2S)-1-((2S,3S)-3-(2-methylbutyl)-4-oxooxetan-2-yl)pentadecan-2-yl formylleucinate 1-(3,5-dichlorophenyl)-2,2,2-trifluoroethane-1-sulfonyl chloride S-(1-(3,5-dichlorophenyl)-2,2,2-trifluoroethyl) ethanethioateRelated products of tetrahydrofuran
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