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99-24-1,MFCD00002194
Catalog No.:AA003562

99-24-1 | methyl 3,4,5-trihydroxybenzoate

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10g
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$7.00   $5.00
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25g
98%
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100g
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003562
Chemical Name:
methyl 3,4,5-trihydroxybenzoate
CAS Number:
99-24-1
Molecular Formula:
C8H8O5
Molecular Weight:
184.1461
MDL Number:
MFCD00002194
SMILES:
COC(=O)c1cc(O)c(c(c1)O)O
NSC Number:
363001
Properties
Properties
 
BP:
450.1°C at 760 mmHg  
Form:
Solid  
MP:
201-204 °C  
Refractive Index:
1.5690 (estimate)  
Solubility:
ethanol: 50 mg/mL, clear  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
0.9  

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Journal: Free radical biology & medicine 20040501

Title: Modulation of beta-lactam resistance in Staphylococcus aureus by catechins and gallates.

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Journal: Journal of agricultural and food chemistry 20020703

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Journal: Journal of ethnopharmacology 20020601

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Title: Investigation of the release of iron from ferritin by naturally occurring antioxidants.

Journal: Journal of inorganic biochemistry 20020521

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Journal: Journal of agricultural and food chemistry 20020327

Title: Determination of phenolic compounds in rose hip (Rosa canina) using liquid chromatography coupled to electrospray ionisation tandem mass spectrometry and diode-array detection.

Journal: Rapid communications in mass spectrometry : RCM 20020101

Title: Ethyl m-digallate from red maple, Acer rubrum L., as the major resistance factor to forest tent caterpillar, Malacosoma disstria Hbn.

Journal: Journal of chemical ecology 20011201

Title: In vitro activity of polyhydroxycarboxylates against herpesviruses and HIV.

Journal: Antiviral chemistry & chemotherapy 20011101

Title: Inhibitory activity for chitin synthase II from Saccharomyces cerevisiae by tannins and related compounds.

Journal: Planta medica 20010801

Title: The kinetics and mechanisms of the reaction of iron(III) with gallic acid, gallic acid methyl ester and catechin.

Journal: Journal of inorganic biochemistry 20010601

Title: [Effect of gallic acid derivatives on secretion of Th1 cytokines and Th2 cytokines from anti CD3-stimulated spleen cells].

Journal: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010601

Title: Use of methanolysis for the determination of total ellagic and gallic acid contents of wood and food products.

Journal: Journal of agricultural and food chemistry 20010301

Title: The kinetics and mechanisms of the reactions of aluminium(III) with gallic acid, gallic acid methyl ester and adrenaline.

Journal: Journal of inorganic biochemistry 20010301

Title: Antioxidant capacity of phenolic and related compounds: correlation among electrochemical, visible spectroscopy methods and structure-antioxidant activity.

Journal: Redox report : communications in free radical research 20010101

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Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20010101

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Journal: Journal of ethnopharmacology 19990101

Title: A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase.

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Title: Kang MS, et al. Inhibitory effect of methyl gallate and gallic acid on oral bacteria. J Microbiol. 2008 Dec;46(6):744-50.

Title: Hsieh TJ, et al. Protective effect of methyl gallate from Toona sinensis (Meliaceae) against hydrogen peroxide-induced oxidative stress and DNA damage in MDCK cells. Food Chem Toxicol. 2004 May;42(5):843-50.

Title: Lee H, et al. Methyl gallate exhibits potent antitumor activities by inhibiting tumor infiltration of CD4+CD25+ regulatory T cells. J Immunol. 2010 Dec 1;185(11):6698-705.

Title: Wang CR, et al. First report on isolation of methyl gallate with antioxidant, anti-HIV-1 and HIV-1 enzyme inhibitory activities from a mushroom (Pholiota adiposa). Environ Toxicol Pharmacol. 2014 Mar;37(2):626-37.

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Tags:99-24-1 Molecular Formula|99-24-1 MDL|99-24-1 SMILES|99-24-1 methyl 3,4,5-trihydroxybenzoate |Organic_Building_Blocks