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Gallic acid

CAS 149-91-7C7H6O5MW 170.12

Gallic acid (CAS 149-91-7) — formula C7H6O5, molecular weight 170.12; category organic chemicals.

Product Overview

CAS Number149-91-7
Molecular FormulaC7H6O5
Molecular Weight170.12
Melting Point258 - 265 °C
Boiling Point501.00 °C. @ 760.00 mm Hg
LogPlog Kow = 0.70
ApplicationsUses: Used to make gallic acid esters, tannins, paper, pyrogallol, and inks, as photographic developer, in tanning and dyeing, to test for free mineral acids, dihydroxyacetone, and alkaloids, in pharmaceuticals, in engraving of lithography, as an analytical reagent, and as a veterinary antidiarrheal, [HSDB], Pulp and Paper Processing [Category: Industry], Leather Tanning and Processing [Category: Industry], Photographic Processing [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], MANUFAC GALLIC ACID ESTERS, PYROGALLOL, INKS, AS PHOTOGRAPHIC DEVELOPER, IN TANNING, IN DYEING, IN TESTING FOR FREE MINERAL ACIDS, DIHYDROXYACETONE AND ALKALOIDS. ESTERS AS ANTIOXIDANTS. FORMERLY AS ASTRINGENT, STYPTIC., Photography, writing ink, dyeing, manufacture of pyrogallol, a tanning agent and a manufacture of tannins, paper manufacture, pharmaceuticals, engraving of lithography, analytical reagent, Used as chemical intermediate for the synthesis of bismuth subgallate, dodecyl gallate, n-octyl gallate, n-propyl gallate, pyrogallol., Gallic acid has been used in the treatment of various diseases for thousands of years. It has pharmacological potential in the regulation of several molecular and cellular processes, e.g., apoptosis and autophagy. Also, gallic acid has been investigated in the treatment of Cardiovascular Diseases (CVDs) in vivo and in vitro., Gallic acid is a natural phenolic compound found in several fruits and medicinal plants, and is reported to have several health-promoting effects. Several of the beneficial effects reported for gallic acid include antioxidant, anti-inflammatory, and antineoplastic properties. It has been reported to have therapeutic activities in gastrointestinal, neuropsychological, metabolic, and cardiovascular disorders. The evidence supporting the pharmacological and therapeutic applications of gallic acid in multiple health complications is limited to cellular and animal studies, and further work is needed to define the safety and therapeutic efficacy in humans., Use Classification: Cosmetics -> Antioxidant, Industry Uses: Cleaning agent, Methods of Manufacturing: CHEMICAL OR ENZYMATIC HYDROLYSIS OF TANNINS FROM NUTGALLS OR TARA POWDER, OBTAINED BY ALKALINE OR ACID HYDROLYSIS OF THE TANNINS FROM NUTGALLS, ALSO BY ENZYMATIC HYDROLYSIS USING SPENT BROTHS FROM PENICILLIUM GLAUCUM OR ASPERGILLUS NIGER WHICH CONTAIN TANNASE., FROM TANNIN CONTAINING MATERIALS. SYNTHESIS FROM ALIPHATIC MATERIALS., p-Hydroxybenzoic acid (sulphonation, alkali fusion), Action of mold on solutions of tannin or by boiling latter with strong acid or caustic soda, Formulations, Preparations: GALLIC ACID, POTASSIUM CHLORATE & RED GUM (FORMULA 156) IS A PYROTECHNIC WHISTLE COMPOSITION., Available as the monohydrate, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, U.S. Imports: (1979) 3.54X10+6 GRAMS, General Manufacturing Information: All Other Basic Inorganic Chemical Manufacturing, Benzoic acid, 3, 4, 5-trihydroxy-: ACTIVE, INCOMPATIBILITIES: FERRIC SALTS (BLUISH-BLACK PPT), CHLORATES, PERMANGANATE, AMMONIA, LEAD ACETATE, ALKALI HYDROXIDES AND CARBONATES, OPIUM IN SOLN, SILVER SALTS, OXIDIZING AGENTS, SPIRIT NITROUS ETHER.
CategoryOrganic Chemicals

Applications

Documented applications: Uses: Used to make gallic acid esters, tannins, paper, pyrogallol, and inks, as photographic developer, in tanning and dyeing, to test for free mineral acids, dihydroxyacetone, and alkaloids, in pharmaceuticals, in engraving of lithography, as an analytical reagent, and as a veterinary antidiarrheal, [HSDB], Pulp and Paper Processing [Category: Industry], Leather Tanning and Processing [Category: Industry], Photographic Processing [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], MANUFAC GALLIC ACID ESTERS, PYROGALLOL, INKS, AS PHOTOGRAPHIC DEVELOPER, IN TANNING, IN DYEING, IN TESTING FOR FREE MINERAL ACIDS, DIHYDROXYACETONE AND ALKALOIDS. ESTERS AS ANTIOXIDANTS. FORMERLY AS ASTRINGENT, STYPTIC., Photography, writing ink, dyeing, manufacture of pyrogallol, a tanning agent and a manufacture of tannins, paper manufacture, pharmaceuticals, engraving of lithography, analytical reagent, Used as chemical intermediate for the synthesis of bismuth subgallate, dodecyl gallate, n-octyl gallate, n-propyl gallate, pyrogallol., Gallic acid has been used in the treatment of various diseases for thousands of years. It has pharmacological potential in the regulation of several molecular and cellular processes, e.g., apoptosis and autophagy. Also, gallic acid has been investigated in the treatment of Cardiovascular Diseases (CVDs) in vivo and in vitro., Gallic acid is a natural phenolic compound found in several fruits and medicinal plants, and is reported to have several health-promoting effects. Several of the beneficial effects reported for gallic acid include antioxidant, anti-inflammatory, and antineoplastic properties. It has been reported to have therapeutic activities in gastrointestinal, neuropsychological, metabolic, and cardiovascular disorders. The evidence supporting the pharmacological and therapeutic applications of gallic acid in multiple health complications is limited to cellular and animal studies, and further work is needed to define the safety and therapeutic efficacy in humans., Use Classification: Cosmetics -> Antioxidant, Industry Uses: Cleaning agent, Methods of Manufacturing: CHEMICAL OR ENZYMATIC HYDROLYSIS OF TANNINS FROM NUTGALLS OR TARA POWDER, OBTAINED BY ALKALINE OR ACID HYDROLYSIS OF THE TANNINS FROM NUTGALLS, ALSO BY ENZYMATIC HYDROLYSIS USING SPENT BROTHS FROM PENICILLIUM GLAUCUM OR ASPERGILLUS NIGER WHICH CONTAIN TANNASE., FROM TANNIN CONTAINING MATERIALS. SYNTHESIS FROM ALIPHATIC MATERIALS., p-Hydroxybenzoic acid (sulphonation, alkali fusion), Action of mold on solutions of tannin or by boiling latter with strong acid or caustic soda, Formulations, Preparations: GALLIC ACID, POTASSIUM CHLORATE & RED GUM (FORMULA 156) IS A PYROTECHNIC WHISTLE COMPOSITION., Available as the monohydrate, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, U.S. Imports: (1979) 3.54X10+6 GRAMS, General Manufacturing Information: All Other Basic Inorganic Chemical Manufacturing, Benzoic acid, 3, 4, 5-trihydroxy-: ACTIVE, INCOMPATIBILITIES: FERRIC SALTS (BLUISH-BLACK PPT), CHLORATES, PERMANGANATE, AMMONIA, LEAD ACETATE, ALKALI HYDROXIDES AND CARBONATES, OPIUM IN SOLN, SILVER SALTS, OXIDIZING AGENTS, SPIRIT NITROUS ETHER..

Technical Profile

What this product is

Gallic acid is a carbon-based organic compound with CAS registry number 149-91-7 and molecular formula C7H6O5 (molecular weight 170.12), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 149-91-7

Its molecular formula C7H6O5 comprises 7 C, 6 H, 5 O atoms.

Also known as: Gallic acid · 没食子酸

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Gallic acid?

The CAS registry number of Gallic acid is 149-91-7.

What is the molecular formula and molecular weight of Gallic acid?

Molecular formula C7H6O5, molecular weight 170.12.

What other names is Gallic acid known by?

It is also registered under: Gallic acid, 没食子酸.

What are the documented applications of Gallic acid?

Recorded applications: Uses: Used to make gallic acid esters, tannins, paper, pyrogallol, and inks, as photographic developer, in tanning and dyeing, to test for free mineral acids, dihydroxyacetone, and alkaloids, in pharmaceuticals, in engraving of lithography, as an analytical reagent, and as a veterinary antidiarrheal, [HSDB], Pulp and Paper Processing [Category: Industry], Leather Tanning and Processing [Category: Industry], Photographic Processing [Category: Other], Textiles (Printing, Dyeing, or Finishing) [Category: Industry], MANUFAC GALLIC ACID ESTERS, PYROGALLOL, INKS, AS PHOTOGRAPHIC DEVELOPER, IN TANNING, IN DYEING, IN TESTING FOR FREE MINERAL ACIDS, DIHYDROXYACETONE AND ALKALOIDS. ESTERS AS ANTIOXIDANTS. FORMERLY AS ASTRINGENT, STYPTIC., Photography, writing ink, dyeing, manufacture of pyrogallol, a tanning agent and a manufacture of tannins, paper manufacture, pharmaceuticals, engraving of lithography, analytical reagent, Used as chemical intermediate for the synthesis of bismuth subgallate, dodecyl gallate, n-octyl gallate, n-propyl gallate, pyrogallol., Gallic acid has been used in the treatment of various diseases for thousands of years. It has pharmacological potential in the regulation of several molecular and cellular processes, e.g., apoptosis and autophagy. Also, gallic acid has been investigated in the treatment of Cardiovascular Diseases (CVDs) in vivo and in vitro., Gallic acid is a natural phenolic compound found in several fruits and medicinal plants, and is reported to have several health-promoting effects. Several of the beneficial effects reported for gallic acid include antioxidant, anti-inflammatory, and antineoplastic properties. It has been reported to have therapeutic activities in gastrointestinal, neuropsychological, metabolic, and cardiovascular disorders. The evidence supporting the pharmacological and therapeutic applications of gallic acid in multiple health complications is limited to cellular and animal studies, and further work is needed to define the safety and therapeutic efficacy in humans., Use Classification: Cosmetics -> Antioxidant, Industry Uses: Cleaning agent, Methods of Manufacturing: CHEMICAL OR ENZYMATIC HYDROLYSIS OF TANNINS FROM NUTGALLS OR TARA POWDER, OBTAINED BY ALKALINE OR ACID HYDROLYSIS OF THE TANNINS FROM NUTGALLS, ALSO BY ENZYMATIC HYDROLYSIS USING SPENT BROTHS FROM PENICILLIUM GLAUCUM OR ASPERGILLUS NIGER WHICH CONTAIN TANNASE., FROM TANNIN CONTAINING MATERIALS. SYNTHESIS FROM ALIPHATIC MATERIALS., p-Hydroxybenzoic acid (sulphonation, alkali fusion), Action of mold on solutions of tannin or by boiling latter with strong acid or caustic soda, Formulations, Preparations: GALLIC ACID, POTASSIUM CHLORATE & RED GUM (FORMULA 156) IS A PYROTECHNIC WHISTLE COMPOSITION., Available as the monohydrate, U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, U.S. Imports: (1979) 3.54X10+6 GRAMS, General Manufacturing Information: All Other Basic Inorganic Chemical Manufacturing, Benzoic acid, 3, 4, 5-trihydroxy-: ACTIVE, INCOMPATIBILITIES: FERRIC SALTS (BLUISH-BLACK PPT), CHLORATES, PERMANGANATE, AMMONIA, LEAD ACETATE, ALKALI HYDROXIDES AND CARBONATES, OPIUM IN SOLN, SILVER SALTS, OXIDIZING AGENTS, SPIRIT NITROUS ETHER..

Which category does Gallic acid belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Gallic acid (CAS 149-91-7), compiled from public chemistry databases.

Registry identifiers across databases

CAS 号149-91-7
PubChem CID370
分子式C7H6O5
IUPAC 名称3,4,5-trihydroxybenzoic acid
UNII(FDA)632XD903SP

Computed descriptors

Molecular Weight170.12
XLogP30.7
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count1
Exact Mass170.02152329
Monoisotopic Mass170.02152329
Topological Polar Surface Area98
Heavy Atom Count12

Physicochemical values on record

Boiling Point501.00 °C. @ 760.00 mm Hg
Melting Point258 - 265 °C
Solubility11.9 mg/mL at 20 °C
Density1.69 kg/l at 20 °C
DensityDensity = 1.694 g/cu m at 6 °C
Vapor Pressure0.00000012 [mmHg]
LogPlog Kow = 0.70
LogP0.70
LogP0.7
LogP0.72

Synonyms and trade names

Gallic acid; 3,4,5-Trihydroxybenzoic acid; 149-91-7; Benzoic acid, 3,4,5-trihydroxy-; Gallic acid, tech.; Pyrogallol-5-carboxylic acid; Kyselina gallova; DTXSID0020650; NSC-20103; NSC-674319; CHEBI:30778; 632XD903SP; NSC20103; DTXCID60650; Acid, Gallic; Gallic Acid 1520

Regulatory listings held on file

法规与食品接触EU Flavoring substances
Flavoring Agents
CIR / INCI: Antioxidant
GHS 通报统计5.4% (22 / 405)

GHS hazard classification

GHS 通报统计5.4% (22 / 405)
已通报的危害声明H315 (75.1%), H318 (19.3%), H319 (75.3%), H335 (71.9%)

What the public record says

没食子酸 · CAS 149-91-7 · C7H6O5. UNII 632XD903SP. Boiling Point: 501.00 °C. @ 760.00 mm Hg; Melting Point: 258 - 265 °C; Solubility: 11.9 mg/mL at 20 °C.

Source: PubChem / Wikidata; the batch COA governs where values differ.

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