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A propos de cet article
Formule linéaire :
(HO)3C6H2CO2CH3
Numéro CAS:
Poids moléculaire :
184.15
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-741-7
Beilstein/REAXYS Number:
2113180
MDL number:
Service technique
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Laissez-nous vous aiderQuality Segment
assay
98%
mp
201-203 °C (lit.)
SMILES string
COC(=O)c1cc(O)c(O)c(O)c1
InChI
1S/C8H8O5/c1-13-8(12)4-2-5(9)7(11)6(10)3-4/h2-3,9-11H,1H3
InChI key
FBSFWRHWHYMIOG-UHFFFAOYSA-N
General description
Methyl 3,4,5-trihydroxybenzoate, also known as methyl gallate, is a derivative of gallic acid with three hydroxyl groups and an ester linkage, which contributes to its reactivity and solubility in organic solvents. It exhibits strong free radical scavenging activity, which is crucial in preventing oxidative stress in biological systems and enhancing the lifespan of materials. Its natural origin and low toxicity make it suitable for biomedical applications, particularly in drug delivery and tissue engineering.
Application
Methyl 3,4,5-trihydroxybenzoate can be used:
- As a precursor to synthesize nanocomposite drug delivery systems for lung cancer treatment. It has low toxicity and can induce apoptosis by generating free radicals.
- As a starting material to prepare norbornene-based main-chain polymers via ring-opening metathesis polymerization (ROMP), for biomedical uses to coatings and electronics.
- As an additive in the pretreatment of Sugarcane Bagasse for the removal of lignin from biomass and consequently the cellulose hydrolysis. This process helps the use of biomass as energy currency for various biotechnological processes
Mot-clé
Warning
Codes de danger
Mentions de précaution
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Classe de stockage
11 - Combustible Solids
Que se passe-t-il ?
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
EPI (équipement de protection individuelle)
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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