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8.42649

Gallic acid

anhydrous, for synthesis

Synonym(s):

Gallic acid

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25 g
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$39.40
250 g
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$129.00

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)

$39.40


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grade

anhydrous

Quality Segment

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


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Pictograms

Exclamation mark

Signal Word

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

Hazard Codes



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