8.42649
Gallic acid
anhydrous, for synthesis
Synonym(s):
Gallic acid
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About This Item
Empirical Formula (Hill Notation):
C7H6O5
CAS Number:
Molecular Weight:
170.12
UNSPSC Code:
12352106
EC Index Number:
205-749-9
NACRES:
NA.22
MDL number:
Assay:
≥98.0% (acidimetric)
grade
anhydrous
Quality Level
assay
≥98.0% (acidimetric)
storage temp.
2-30°C
SMILES string
Oc1c(cc(cc1O)C(=O)O)O
InChI
1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12)
InChI key
LNTHITQWFMADLM-UHFFFAOYSA-N
General description
(anhydrous) for synthesis
Application
- Gallic acid in tumor-targeted therapy: A study described the use of gallic acid-loaded HFZIF-8 nanoparticles for enhanced tumor-targeted delivery and thermal-catalytic therapy, showcasing potential applications in cancer treatment strategies (Yang et al., 2024).
- Gallic acid in industrial processes: Research highlighted the integration of gallic acid within porous sponges for efficient dye adsorption and emulsion separation, indicating its utility in environmental and industrial applications (Yan et al., 2024).
- Gallic acid in extraction processes: The use of gallic acid was explored in the ultrasound-assisted extraction of bioactive pigments from Spirulina platensis, employing natural deep eutectic solvents to enhance extraction efficiency and safety (Martins et al., 2023).
- Gallic acid in self-healing materials: A novel study developed a self-healing hydrogel using gallic acid and carboxymethyl cellulose, triggered by Fe(3+) coordination cross-linking, demonstrating innovative applications in materials science (Yang et al., 2024).
Analysis Note
Assay (acidimetric): ≥ 98.0 %
Identity (IR): passes test
Identity (IR): passes test
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Warning
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
hcodes
Certificates of Analysis (COA)
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