T69000
3,4,5-Trimethoxybenzoic acid
ReagentPlus®, 99%
Sinonimo/i:
Gallic acid trimethyl ether, Trimethylgallic acid
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About This Item
Prodotti consigliati
Livello qualitativo
Nome Commerciale
ReagentPlus®
Saggio
99%
P. eboll.
225-227 °C/10 mmHg (lit.)
Punto di fusione
168-171 °C (lit.)
Stringa SMILE
COc1cc(cc(OC)c1OC)C(O)=O
InChI
1S/C10H12O5/c1-13-7-4-6(10(11)12)5-8(14-2)9(7)15-3/h4-5H,1-3H3,(H,11,12)
SJSOFNCYXJUNBT-UHFFFAOYSA-N
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Categorie correlate
Note legali
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(3-4), 988-992 (2006-05-09)
The interaction between 3,4,5-trimethoxybenzoic acid (TMBA) and bovine serum albumin (BSA) was studied by fluorescence and UV-vis absorption spectroscopy. In the mechanism discussion, it was proved that the fluorescence quenching of BSA by TMBA is a result of the formation
Bioscience, biotechnology, and biochemistry, 60(6), 1049-1050 (1996-06-01)
Bioassay-guided fractionation of the MeOH extract of Ornithogalum saundersiae bulbs led to the isolation of a new cholestane bisdesmoside with potent cytotoxic activities toward leukemia HL-60 and MOLT-4 cells. The structure was deduced mainly from spectroscopic information.
[Synthesis and the study of the effect of new 3,4,5-trimethoxybenzoic acid derivatives on the central nervous system].
Acta poloniae pharmaceutica, 42(2), 117-122 (1985-01-01)
The Journal of experimental zoology, 244(1), 133-143 (1987-10-01)
In the amphibian ovarian follicle, progesterone production is thought to induce maturation of the enclosed oocyte. Intracellular mechanisms regulating these events in the somatic and germ cells are incompletely understood. However, calcium appears to play a role in the production
Polish journal of pharmacology and pharmacy, 33(3), 365-371 (1981-10-01)
Craviten hydrolysis in vitro was studied in human, rat and canine plasma and erythrocytes. Craviten was degraded during the incubation with plasma and the hydrolysis was inhibited by trimethoxybenzoic acid, a metabolite of Craviten. Erythrocyte enzymes do not participate in
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