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Merck

27645

Sigma-Aldrich

Gallic acid monohydrate

≥99% (HPLC)

Sinónimos:

3,4,5-Trihydroxybenzoic acid monohydrate

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About This Item

Fórmula lineal:
(HO)3C6H2CO2H · H2O
Número de CAS:
Peso molecular:
188.13
Beilstein:
2050274
Número CE:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.21

Nivel de calidad

Análisis

≥99% (HPLC)

formulario

solid

impurezas

7-12% water (Karl Fischer)

residuo de ign.

≤0.1% (as SO4)

mp

252 °C (dec.) (lit.)

trazas de anión

chloride (Cl-): ≤200 mg/kg
sulfate (SO42-): ≤100 mg/kg

cadena SMILES

OC(=O)c1cc(O)c(O)c(O)c1

InChI

1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12)/p-1

Clave InChI

LNTHITQWFMADLM-UHFFFAOYSA-M

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Descripción general

Gallic acid monohydrate is a phenolic acid. It is a planar molecule with two intramolecular hydrogen bonds and five intermolecular hydrogen bonds.

Aplicación

Gallic acid monohydrate can be used as a reducing agent to synthesize Tin oxide (SnO2) nanoparticles via the precipitation method using stannous chloride as a precursor salt.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

482.0 °F - closed cup

Punto de inflamabilidad (°C)

250 °C - closed cup

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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Ulyana Muñoz Acuña et al.
Journal of natural products, 73(11), 1775-1779 (2010-10-30)
Two new polyisoprenylated benzophenones, 32-hydroxy-ent-guttiferone M (1) and 6-epi-guttiferone J (2), along with seven known compounds, 6-epi-clusianone (3), guttiferone A (4), xanthochymol (5), guttiferone E (6), isoxanthochymol (7), (+)-volkensiflavone (8), and (+)-morelloflavone (9), were identified from the seeds and rinds
Claudriana Locatelli et al.
Bioorganic & medicinal chemistry, 16(7), 3791-3799 (2008-02-26)
Gallic acid and gallates with the same number of hydroxyl groups and varying the length of the side carbon chain, with respective lipophilicity being defined through the ClogP values, were examined for their ability to induce apoptosis (through the DNA
Cristina Medina-Plaza et al.
Molecules (Basel, Switzerland), 24(18) (2019-09-22)
The effects of temperature and ethanol concentration on the kinetics of anthocyanin adsorption and desorption interactions with five cell wall materials (CWM) of different composition were investigated. Using temperatures of 15 °C and 30 °C and model wine with ethanol
Kristina Habschied et al.
Foods (Basel, Switzerland), 9(2) (2020-02-28)
Antioxidative molecules, such as polyphenols can preserve and prolong the freshness of packaged beers. The aim of this work was to assess the content of polyphenolic compounds (by Folin-Ciocalteu and standard European Brewery Convention method) in different types of industrially
Tarik El-Sayed Ali
European journal of medicinal chemistry, 44(11), 4385-4392 (2009-07-10)
The reaction of 5,6-diphenyl-3-hydrazino-1,2,4-triazine (1) with bis(methylthio)methylene]malononitrile (2) afforded 5-amino-1-(5,6-diphenyl-1,2,4-triazin-3-yl)-3-(methylthio)-1H-pyrazole-4-carbonitrile (3). Compound 3 reacted with thiourea to give 3,4-diaminopyrazolo[3,4-d]pyrimidine 5, which was treated with benzoyl chloride to give pyrazolo[5,4,3-kl]pyrimido[4,3-d]pyrimidine 6. Treatment of 3 with acetic anhydride produced 3-methylthio-pyrazolo[3,4-d]pyrimidine derivative 7

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