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Merck

G5129

Sigma-Aldrich

Gentisic acid sodium salt hydrate

≥98%

Synonim(y):

2,5-Dihydroxybenzoic acid sodium salt, 5-Hydroxysalicylate sodium

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About This Item

Wzór liniowy:
C7H5O4Na
Numer CAS:
Masa cząsteczkowa:
176.10
Numer WE:
Numer MDL:
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
NACRES:
NA.22

Próba

≥98%

ciąg SMILES

[Na].Oc1ccc(O)c(c1)C(O)=O

InChI

1S/C7H6O4.Na.H2O/c8-4-1-2-6(9)5(3-4)7(10)11;;/h1-3,8-9H,(H,10,11);;1H2/q;+1;/p-1

Klucz InChI

SYGYBOPDUUSVNE-UHFFFAOYSA-M

Zastosowanie

Reactant involved in oxidative coupling reactions followed by the product use as an antioxidant and tyrosinase inhibitor
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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


Certyfikaty analizy (CoA)

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PloS one, 7(7), e38701-e38701 (2012-07-19)
Gentisate (2,5-dihydroxybenzoate) is a key ring-cleavage substrate involved in various aromatic compounds degradation. Corynebacterium glutamicum ATCC13032 is capable of growing on gentisate and genK was proposed to encode a transporter involved in this utilization by its disruption in the restriction-deficient
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Matrix-assisted laser desorption/ionization (MALDI) is a powerful technique for the direct analysis of lipids in complex mixtures and thin tissue sections, making it an extremely attractive method for profiling lipids in health and disease. Lipids are readily detected as [M+H](+)
Ravi Joshi et al.
Free radical research, 46(1), 11-20 (2011-10-26)
Abstract Antioxidant activity of gentisic acid has been studied using fast chemical kinetics and two in vitro models, namely the isolated rat liver mitochondria (RLM) and the human erythrocytes. The presence of gentisic acid (GA) during irradiation significantly reduced the
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