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Lauryl gallate
CAS No. 1166-52-5
Lauryl gallate( Nipagallin LA | Progallin LA | NSC 133463 | NSC-133463 | NSC133463 )
Catalog No. M23341 CAS No. 1166-52-5
Lauryl gallate is the ester of gallic acid and dodecanol. As a food additive, it is used as a preservative and antioxidant.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | In Stock |
|
| 200MG | 27 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameLauryl gallate
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NoteResearch use only, not for human use.
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Brief DescriptionLauryl gallate is the ester of gallic acid and dodecanol. As a food additive, it is used as a preservative and antioxidant.
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DescriptionLauryl gallate is the ester of gallic acid and dodecanol. As a food additive, it is used as a preservative and antioxidant.
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In VitroDodecyl gallate (Lauryl gallate) is an ester derivative of gallic acid, a natural plant phenolic compound. Dodecyl gallate (Lauryl gallate) protects cells from oxidative stress, in a process associated with radical scavenging, inhibition of enzymes involved in lipid peroxidation, and increasing expression of antioxidant genes. Due to its hydrophobic properties, Dodecyl gallate can disrupt biomembranes and cause protein inactivation.
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In Vivo——
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SynonymsNipagallin LA | Progallin LA | NSC 133463 | NSC-133463 | NSC133463
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number1166-52-5
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Formula Weight338.44
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Molecular FormulaC19H30O5
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Purity>98% (HPLC)
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SolubilityDMSO:60 mg/mL (177.28 mM)
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SMILESO=C(OCCCCCCCCCCCC)C1=CC(O)=C(O)C(O)=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Feuser PE, Arévalo JM, Junior EL, Rossi GR, da Silva Trindade E, Rocha ME, Jacques AV, Ricci-Júnior E, Santos-Silva MC, Sayer C, de Araújo PH. Increased cellular uptake of lauryl gallate loaded in superparamagnetic poly(methyl methacrylate) nanoparticles due to surface modification with folic acid. J Mater Sci Mater Med. 2016 Dec;27(12):185. Epub 2016 Oct 27. PubMed PMID: 27787810.
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