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Malic acid (E 296) Sale

(Synonyms: DL-苹果酸; Hydroxybutanedioic acid; E 296) 目录号 : GC33608

The racemate of L-malic acid

Malic acid (E 296) Chemical Structure

Cas No.:6915-15-7

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5g
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产品描述

DL-Malic acid is the racemate of the metabolic intermediate L-malic acid.1 It reduces CCL2 and ICAM expression induced by IFN-γ and TNF-α in HaCaT human keratinocytes when used at a concentration of 1 mM.2 Topical administration of DL-malic acid (10 mM) inhibits epidermis and dermis thickening, as well as mast cell and eosinophil dermal infiltration in a mouse model of atopic dermatitis induced by 2,4-dinitrochlorobenzene (DNBC). Formulations containing DL-malic acid have been used as food and cosmetic preservatives and acidity regulators.

1.Ryan, D.G., Murphy, M.P., Frezza, C., et al.Coupling Krebs cycle metabolites to signalling in immunity and cancerNat. Metab.116-33(2019) 2.Lee, B., Heo, J., Hong, S., et al.??-Malic acid as a component of α-hydroxy acids: Effect on 2,4-dinitrochlorobenzene-induced inflammation in atopic dermatitis-like skin lesions in vitro and in vivoImmunopharmacol. Immunotoxicol.41(6)614-621(2019)

Chemical Properties

Cas No. 6915-15-7 SDF
别名 DL-苹果酸; Hydroxybutanedioic acid; E 296
Canonical SMILES O=C(O)C(O)CC(O)=O
分子式 C4H6O5 分子量 134.09
溶解度 DMF: 30 mg/ml,DMSO: 30 mg/ml,PBS (pH 7.2): 10 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 7.4577 mL 37.2884 mL 74.5768 mL
5 mM 1.4915 mL 7.4577 mL 14.9154 mL
10 mM 0.7458 mL 3.7288 mL 7.4577 mL
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Research Update

A new deep eutectic solvent-agarose gel with hydroxylated fullerene as electrical "switch" system for drug release

Carbohydr Polym 2022 Nov 15;296:119939.PMID:36087988DOI:10.1016/j.carbpol.2022.119939

A novel portable conductive system of hydroxylated fullerene (TEGs-C60) embedded on the deep eutectic solvent (DES, choline chloride/Malic acid)-agarose gel was developed for on-demand curation with skin contact. It has been found with better elasticity, conductivity and thermal stability than agarose hydrogel. Especially, the electro-responsive drug releasing amount on the skin of mice and live rabbits through small batteries was proved to be 4-5 times of those without electrical stimulation, which reached the level of clinic daily dosage. Meanwhile, it also showed good biocompatibility and much higher antibacterial rate against S. aureus (78.67 ± 0.80 %) together with E. coli (92.08 ± 1.50 %) than those of commercial chitosan gel. The new electrical "switch" gel system provided an effective and useful development strategy for advanced drug delivery.