Gallic acid

Modify Date: 2026-06-30 19:58:34

Gallic acid Structure
Gallic acid structure
Common Name Gallic acid
CAS Number 149-91-7 Molecular Weight 170.120
Density 1.7±0.1 g/cm3 Boiling Point 501.1±50.0 °C at 760 mmHg
Molecular Formula C7H6O5 Melting Point 252 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 271.0±26.6 °C

 Use of Gallic acid


Gallic acid is an antioxidant which can inhibit both COX-2.

Summary: Gallic acid, also known as 3,4,5-trihydroxybenzoic acid, has a CAS number of 149-91-7, with a molecular formula of C7H6O5 and a molecular weight of 170.120. It appears as a white crystalline powder with a melting point of 252°C (dec.). For use in antibacterial, hemostatic, antidiarrheal, and preservative applications, as well as in the preparation of chemical reagents, pharmaceuticals, inks, dyes, food, light industry, and organic synthesis. For research-use only, not for medical or clinical usage.


 Names

This table lists Chinese names, IUPAC names and various aliases of this chemical substance.

Name gallic acid
Synonym More Synonyms

 Gallic acid Biological Activity

This table contains bioactivity, target information and biological‑assay experimental data of this compound.

Description Gallic acid is an antioxidant which can inhibit both COX-2.
Related Catalog
Target

COX-2

In Vitro Gallic acid is an antioxidant which can inhibit both COX-2[1]. After 18 h treatment with Gallic acid, the number of viable neutrophils is dramatically decreased from 40.3% to 27.7%, highly comparable with 26.4% for untreated neutrophils. Gallic acid fails to attenuate isoproterenol-induced myocytolysis[3].
In Vivo The food intake (2.6±0.08 g/day, p=0.69) and the body weight (2.5±0.69 g, p=0.76) of the Gallic acid group do not differ significantly from those of the control group (food intake; 2.41±0.14 g/day and the body weight; 2.83±0.84 g/day). The blood glucose tolerance in the Gallic acid group is significantly improved after 2 weeks of treatment. The blood glucose tolerance of the Gallic acid group after a treatment period of 2 weeks is also significantly better than that of the control group at 90 and 120 min ( p<0.05). The serum triglyceride concentration in the Gallic acid group (0.67±0.03 mM, p<0.05) is significantly reduced relative to that of the control group (1.08±0.20 mM). The total cholesterol concentration is similar in the control (3.19±0.27 mM) and Gallic acid (3.01±0.18 mM) groups[2].
Cell Assay Neutrophils are treated with 8 μg/mL Gallic acid in RPMI1640/10% FBS for 3, 6, 9, and 18 h. At the end of Gallic acid treatment, the cells are stained with Annexin V-FITC and PI according to manufacturer's instructions. Briefly, the cells are washed twice with ice-cold PBS and resuspended in 1× Binding Buffer at a concentration of 1×106 cells/mL. Cell suspensions (1×105 cells in 100 μL) are incubated with 5 μL of Annexin V-FITC and 10 μL PI in a 5 mL culture tube at room temperature for 20 min. The stained cells are immediately analyzed on flow cytometry system[3].
Animal Admin Five-week-old male C57BL/6 mice are used in this study. The animals are maintained in a temperature-controlled room at 22° C on a 12 h light-dark photocycle. The mice are divided into the control vehicle group and the Gallic acid group. For 2 weeks, the mice are administered intraperitoneal treatment on a daily basis with vehicle (10% alcohol, 10% tween 80, and 80% saline) alone or with 10 mg/kg Gallic acid. After this treatment, GTTs are again conducted, and the blood samples are taken for subsequent biochemical analysis. Over the experimental period, food intake and body weight are measured on a daily basis[2].
References

[1]. Amaravani M, et al. COX-2 structural analysis and docking studies with gallic acid structural analogues. Springerplus. 2012 Dec;1(1):58.

[2]. Bak EJ, et al. Gallic acid improves glucose tolerance and triglyceride concentration in diet-induced obesity mice. Scand J Clin Lab Invest. 2013 Dec;73(8):607-14.

[3]. Cheng Y, et al. Plant Natural Products Calycosin and Gallic Acid Synergistically Attenuate Neutrophil Infiltration and Subsequent Injury in Isoproterenol-Induced Myocardial Infarction: A Possible Role for Leukotriene B4 12-Hydroxydehydrogenase? Oxid Med Cell Longev. 2015;2015:434052.

 Chemical & Physical Properties

This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.

Density 1.7±0.1 g/cm3
Boiling Point 501.1±50.0 °C at 760 mmHg
Melting Point 252 °C (dec.)(lit.)
Molecular Formula C7H6O5
Molecular Weight 170.120
Flash Point 271.0±26.6 °C
Exact Mass 170.021530
PSA 97.99000
LogP 0.91
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.730
Stability Stability Stable, but may discolour upon exposure to light. Hygroscopic. Incompatible with strong oxidizing agents, strong bases, acid chlorides, acid anhydrides.
Water Solubility 12 g/L cold water

 MSDS

This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.

 Toxicological Information

This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LW7525000
CHEMICAL NAME :
Gallic acid
CAS REGISTRY NUMBER :
149-91-7
BEILSTEIN REFERENCE NO. :
2050274
LAST UPDATED :
199701
DATA ITEMS CITED :
12
MOLECULAR FORMULA :
C7-H6-O5
MOLECULAR WEIGHT :
170.13
WISWESSER LINE NOTATION :
QVR CQ DQ EQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
4300 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
320 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
5 gm/kg
TOXIC EFFECTS :
Lungs, Thorax, or Respiration - chronic pulmonary edema Liver - other changes Kidney, Ureter, Bladder - other changes
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
DOSE :
5 mg/kg
SEX/DURATION :
female 1 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Maternal Effects - ovaries, fallopian tubes
TYPE OF TEST :
Cytogenetic analysis

MUTATION DATA

TYPE OF TEST :
Cytogenetic analysis
TEST SYSTEM :
Rodent - hamster Ovary
DOSE/DURATION :
50 mg/L
REFERENCE :
CALEDQ Cancer Letters (Shannon, Ireland). (Elsevier Scientific Pub. Ireland Ltd., POB 85, Limerick, Ireland) V.1- 1975- Volume(issue)/page/year: 14,251,1981 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 84280 No. of Facilities: 549 (estimated) No. of Industries: 21 No. of Occupations: 10 No. of Employees: 2520 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - 84280 No. of Facilities: 294 (estimated) No. of Industries: 14 No. of Occupations: 8 No. of Employees: 2184 (estimated) No. of Female Employees: 252 (estimated)

 Safety Information

This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.

Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36-S24/25
RIDADR NONH for all modes of transport
WGK Germany 2
RTECS LW7525000
HS Code 2918290000

 Synthetic Route

This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.

 Customs

This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.

HS Code 2918290000
Summary HS: 2918290000 other carboxylic acids with phenol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) VAT:17.0% MFN tariff:6.5% General tariff:30.0%

 Articles394

More Articles

This table lists relevant public references with title, journal and publication metadata for this compound.

Urinary metabolic fingerprinting of mice with diet-induced metabolic derangements by parallel dual secondary column-dual detection two-dimensional comprehensive gas chromatography.

J. Chromatogr. A. 1361 , 265-76, (2014)

This study investigates the potential of a parallel dual secondary column-dual detection two-dimensional comprehensive GC platform (GC×2GC-MS/FID) for metabolic profiling and fingerprinting of mouse u...

Vegetables' juice influences polyol pathway by multiple mechanisms in favour of reducing development of oxidative stress and resultant diabetic complications.

Pharmacogn. Mag. 10(Suppl 2) , S383-91, (2014)

Hyperglycemia induced generation of free radicals and consequent development of oxidative stress by polyol pathway is one of the crucial mechanisms stirring up development of diabetic complications. W...

Antimicrobial activity of natural products from the flora of Northern Ontario, Canada.

Pharm. Biol. 53(6) , 800-6, (2015)

The number of multidrug resistant (MDR) microorganisms is increasing and the antimicrobial resistance expressed by these pathogens is generating a rising global health crisis. In fact, there are only ...

 Synonyms

This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.

3,4,5-trihydroxybenzenoic Acid
Gallic acid
graphite oxide
kyselinagallova
3,4,5-Trihydroxy-benzoic acid
Acid, Gallic
BETZ 0276
3,4,5-Trihydroxybenzoic acid
gallic
Galloyl alcohol
MFCD00002510
Gallussaure
graphitic acid
3-10-00-02070 (Beilstein Handbook Reference)
EINECS 205-749-9

 Gallic acid | FAQ

This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.

Q: What is the molecular formula of gallic acid?
A: Molecular formula of gallic acid is C7H6O5.
Q: What are the upstream materials of gallic acid?
A: Related upstream materials(CAS) of gallic acid: 99-24-1;118-41-2;989-51-5;14937-32-7;71-23-8;53209-27-1;131189-57-6;121-79-9;79786-01-9;2922-42-1.
Q: What is the melting point of gallic acid?
A: Melting point of gallic acid is 252 °C (dec.)(lit.).
Q: What is the CAS number of gallic acid?
A: CAS number of gallic acid is 149-91-7.
Q: What is the English name of gallic acid?
A: The English name of gallic acid is gallic acid.
Q: What is the LogP of gallic acid?
A: LogP of gallic acid is 0.91.
Q: What are the uses of gallic acid?
A: Main uses of gallic acid: Gallic acid is an antioxidant which can inhibit both COX-2.
Q: What is the boiling point of gallic acid?
A: Boiling point of gallic acid is 501.1±50.0 °C at 760 mmHg.
Q: What English synonyms does gallic acid have?
A: English synonyms of gallic acid: 3,4,5-trihydroxybenzenoic Acid, Gallic acid, graphite oxide, kyselinagallova, 3,4,5-Trihydroxy-benzoic acid, Acid, Gallic, BETZ 0276, 3,4,5-Trihydroxybenzoic acid, gallic, Galloyl alcohol, MFCD00002510, Gallussaure, graphitic acid, 3-10-00-02070 (Beilstein Handbook Reference), EINECS 205-749-9.
Q: What is the polar surface area (PSA) of gallic acid?
A: Polar surface area (PSA) of gallic acid is 97.99000.

 Gallic acidfactory

This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.

Shanghai Nianxing Industrial Co., Ltd
BioBioPha
Dayang Chem (Hangzhou) Co., Ltd.
naturewill
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