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Gallic acid

$43

  • Brand : BIOFRON

  • Catalogue Number : BF-G3008

  • Specification : 98%

  • CAS number : 149-91-7

  • Formula : C7H6O5

  • Molecular Weight : 170.12

  • PUBCHEM ID : 370

  • Volume : 50mg

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Catalogue Number

BF-G3008

Analysis Method

HPLC,NMR,MS

Specification

98%

Storage

2-8°C

Molecular Weight

170.12

Appearance

White crystalline powder

Botanical Source

Cynomorium songaricum,Punica granatum,Paeonia lactiflora,Paeonia suffruticosa,Chaenomeles speciosa

Structure Type

Phenolics

Category

Standards;Natural Pytochemical;API

SMILES

C1=C(C=C(C(=C1O)O)O)C(=O)O

Synonyms

3,4,5-trihydroxybenzenoic Acid/Gallic acid/Benzoic acid, 3,4,5-trihydroxy-/graphite oxide/kyselinagallova/3,4,5-Trihydroxy-benzoic acid/Acid, Gallic/BETZ 0276/2050274/3,4,5-Trihydroxybenzoic acid/gallic/Galloyl alcohol/Gallussaure/graphitic acid/3-10-00-02070 (Beilstein Handbook Reference)

IUPAC Name

3,4,5-trihydroxybenzoic acid

Density

1.7±0.1 g/cm3

Solubility

Methanol

Flash Point

271.0±26.6 °C

Boiling Point

501.1±50.0 °C at 760 mmHg

Melting Point

252 °C (dec.)(lit.)

InChl

InChl Key

WGK Germany

RID/ADR

HS Code Reference

2918290000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:149-91-7) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

PMID

26440222

Abstract

Gallic acid (3,4,5 trihydroxybenzoic acid) is a secondary metabolite present in most plants. This metabolite is known to exhibit a range of bioactivities including antioxidant, antimicrobial, anti-inflammatory, and anticancer. There are various methods to analyze gallic acid including spectrometry, chromatography, and capillary electrophoresis, among others. They have been developed to identify and quantify this active ingredient in most biological matrices. The aim of this article is to review the available information on analytical methods for gallic acid, as well as presenting the advantages and limitations of each technique.

KEYWORDS

Analytical methods; gallic acid; polyphenol.

Title

Gallic Acid: Review of the Methods of Determination and Quantification

Author

Felipe Hugo Alencar Fernandes 1 , Herida Regina Nunes Salgado 1

Publish date

2016 May 3

PMID

26174568

Abstract

Gallic acid and its derivatives have a large number of applications in various fields of science. In nature, these compounds are widely distributed in plants and fruits, and thus they are being used as food stuffs, preservatives, etc. directly or indirectly by human community. They have also been implicated as anticarcinogenic, antimicrobial, antimutagenic, antiangiogenic and anti-inflammatory agents besides their use in treating critical diseases like depression, cancer, microbial infections, lipid-related diseases, etc. Herein, an attempt has been made to summarize the important uses of gallic acid derivatives which have extensively been disclosed particularly in various patents. This review would certainly create a great interest of the scientific community toward the developments and uses of gallic acid based compounds in the future.

KEYWORDS

anti-inflammatory; antiangiogenic; antiarteriosclerosis; antibacterial; anticarcinogenic; anticholesterolemic; antioxidant; apoptosis; gallic acid; melanogenesis.

Title

Medicinal Importance of Gallic Acid and Its Ester Derivatives: A Patent Review

Author

Sneha Choubey 1 , Lesley Rachel Varughese 1 , Vinod Kumar 2 , Vikas Beniwal 1

Publish date

2015

PMID

29076351

Abstract

Aim: Gallic acid and its ester derivatives have shown antifungal activity in vitro. This study was performed to investigate their activity against Candida albicans and their toxicity in the animal models Caenorhabditis elegans and zebrafish embryos.
Results: The compounds protected worms from C. albicans infection. The dodecyl gallate was the most effective. In zebrafish embryo, gallic acid and dodecyl gallate were the least toxic.
Conclusion: Gallic acid and its ester derivatives have potential for in vivo use against C. albicans infection. The antifungal effects and toxicity of gallate esters in these alternative animal models were dependent on carbon chain length.

KEYWORDS

alternative animal models; antifungal development; gallates; gallic acid; infection.

Title

Activity of Gallic Acid and Its Ester Derivatives in Caenorhabditis Elegans and Zebrafish (Danio Rerio) Models

Author

Junya de Lacorte Singulani 1 , Liliana Scorzoni 1 , Paulo Cesar Gomes 1 , Ana Carolina Nazare 2 , Carlos Roberto Polaquini 2 , Luis Octavio Regasini 2 , Ana Marisa Fusco-Almeida 1 , Maria Jose Soares Mendes-Giannini 1

Publish date

2017 Oct


Description :

Gallic acid is an antioxidant which can inhibit both COX-2.