Details:
Gallic acid Basic information |
Product Name: |
Gallic acid |
Synonyms: |
TIMTEC-BB SBB008781;RARECHEM AL BE 0070;3,4,5-trihydroxy-benzoicaci;gallic;Gallussaure;Kyselina 3,4,5-trihydroxybenzoova;Kyselina gallova;kyselina3,4,5-trihydroxybenzoova |
CAS: |
149-91-7 |
MF: |
C7H6O5 |
MW: |
170.12 |
EINECS: |
205-749-9 |
Product Categories: |
Pharmaceutical Intermediates;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Fine chemicals;Food additive,Antioxidant anticorrosive;Inhibitors |
Mol File: |
149-91-7.mol |
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Gallic acid Chemical Properties |
mp |
252 °C (dec.)(lit.) |
density |
1.694 |
Water Solubility |
12 g/L cold water |
Merck |
14,4345 |
BRN |
2050274 |
Stability: |
Stability Stable, but may discolour upon exposure to light. Hygroscopic. Incompatible with strong oxidizing agents, strong bases, acid chlorides, acid anhydrides. |
CAS DataBase Reference |
149-91-7(CAS DataBase Reference) |
NIST Chemistry Reference |
Benzoic acid, 3,4,5-trihydroxy-(149-91-7) |
EPA Substance Registry System |
Benzoic acid, 3,4,5-trihydroxy-(149-91-7) |
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Gallic acid Usage And Synthesis |
Chemical Properties |
white powder |
Usage |
antineoplastic, astringent, antibacterial |
General Description |
Odorless white solid. Sinks in water. |
Air & Water Reactions |
Sparingly water soluble |
Reactivity Profile |
Phenols, such as Gallic acid, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid. |
Health Hazard |
Inhalation of dust may irritate nose and throat. Contact with eyes or skin causes irritation. |
Fire Hazard |
Flash point data for Gallic acid are not available. Gallic acid is probably combustible. |
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Gallic acid Preparation Products And Raw materials |
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