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3,4,5-Trihydroxybenzoesure

Gallic acid

HCID 173204431
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Grundinformationen

CAS
149-91-7
Standard-SMILES
O=C(O)c1cc(O)c([O-])c(O)c1.[H+]
InChIKey
LNTHITQWFMADLM-UHFFFAOYSA-N
Summenformel
C7H6O5
Durchschnittliche Molmasse
170,12 g/mol

Namen und Bezeichner

Bevorzugter Name
Gallic acid
Lokaler Name
3,4,5-Trihydroxybenzoesure
Englischer Name
Gallic acid
Summenformel
C7H6O5
Molmasse
170.12

Namen und Synonyme

3,4,5-TRIHYDROXYBENZOIC ACIDgraphite oxidegallicGallic acid, 98% 250GRGallic acid 0Gallic acid, 98% 5GRGallic acid in WaterAnhydrous gallic acidWater-Soluble GALLIC ACIDNano Liposomal Gallic acid

Datenbank-Bezeichner

CAS
149-91-7
PubChem CID
173204431

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
251 °C · 251 °C (dec.) (lit.)
Siedepunkt
259.73 °C · 259.73°C (rough estimate)
Dichte
1.694 · 1.694
Dampfdruck
0 Pa · 0Pa at 25℃
Brechungsindex
1.569 · 1.5690 (estimate)
storage temp.
2 · 2-8°C
Löslichkeit
Methanol (Slightly), Water (Slightly, Heated)
pka
4.41 · 4.41(at 25℃)
Aggregatzustand
Powder
Farbe
Off-white
PH
3.75 · 3.75(1 mM solution);3.22(10 mM solution);2.71(100 mM solution)
Biologische Quelle
plant fruit
Wasserlöslichkeit
12 g/L · 12 g/L cold water
Merck
14 · 14,4345
BRN
2050274 · 2050274
Henry's Law Constant
1.2 · 1.2×1014 mol/(m3Pa) at 25℃, HSDB (2015)
Stabilität
Stability Stable, but may discolour upon exposure to light. Hygroscopic. Incompatible with strong oxidizing agents, strong bases, acid chlorides, acid anhydrides.
Major Application
agriculturemetabolomicsmicrobiologyvitamins, nutraceuticals, and natural productsvitamins, nutraceuticals, and natural products
Kosmetik-Inhaltsstoffe Funktionen
ANTIOXIDANT
InChI
1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12)
InChIKey
LNTHITQWFMADLM-UHFFFAOYSA-N

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

F
8-9-23
wgk
2
tsca
TSCA listed
hs_code
29182900
RTECS-Nr.
LW7525000
risk_code
36/37/38
Toxizität
LD50 in rabbits (g/kg): 5.0 orally (Dollahite)
hazard_code
Xi
safety_code
26-36-24/25-37/39
Speicherklasse
11 - Combustible Solids
Giftige Stoffe Daten
149-91-7(Hazardous Substances Data)
Hazard Classifications
Eye Irrit. 2Skin Irrit. 2STOT SE 3

Chemie und Industrie

Anwendungen · 4 Einträge

BeschreibungGallic acid is a trihydroxybenzoic acid, a type of phenolic acid, a type of organic acid, also known as 3,4,5- trihydroxy benzoic acid, found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants. The chemical formula is C6H2(OH)3COOH. Gallic acid is found both free and as part of hydrolyzable tannins. Salts and esters of gallic acid are termed 'gallates'. Despite its name, it does not contain gallium. Gallic acid is commonly used in the pharmaceutical industry. It is used as a standard for determining the phenol content of various analytes by the Folin - Ciocalteau assay; results are reported in gallic acid equivalents. Gallic acid can also be used as a starting material in the synthesis of the psychedelic alkaloid mescaline. Gallic acid seems to have anti-fungal and antiviral properties. Gallic acid acts as an antioxidant and helps to protect human cells against oxidative damage. Gallic acid was found to show cytotoxicity against cancer cells, without harming healthy cells. Gallic acid is used as a remote astringent in cases of internal haemorrhage. Gallic acid is also used to treat albuminuria and diabetes. Some ointments to treat psoriasis and external haemorrhoids contain gallic acid.

OccurrenceGallic acid is found in a number of land plants. It is also found in the aquatic plant Myriophyllum spicatum and shows an allelopathic effect on the growth of the blue-green alga Microcystis aeruginosa. In food Areca nut Bearberry (Arctostaphylos sp) Bergenia sp Blackberry Hot chocolate Juglans regia (Common walnut) Mango in peels and leaves Phyllanthus emblica (Indian gooseberry) in fruits Raspberry Syzygium aromaticum (clove) Vinegar wine Witch hazel (Hamamelis virginiana) White tea.

HistoryGallic acid is an important component of iron gall ink, the standard European writing and drawing ink from the 12 th to 19th century with a history extending to the Roman empire and the Dead Sea Scrolls. Pliny the Elder (23-79 AD) describes his experiments with it and writes that it was used to produce dyes. Galls (also known as oak apples) from oak trees were crushed and mixed with water, producing tannic acid (a macromolecular complex containing gallic acid). It could then be mixed with green vitriol (ferrous sulfate) — obtained by allowing sulfate - saturated water from a spring or mine drainage to evaporate — and gum arabic from acacia trees; this combination of ingredients produced the ink.Gallic acid was one of the substances used by Angelo Mai (1782–1854), among other early investigators of palimpsests, to clear the top layer of text off and reveal hidden manuscripts underneath. Mai was the first to employ it, but did so "with a heavy hand", often rendering manuscripts too damaged for subsequent study by other researchers.Early photographers, including Joseph Bancroft Reade (1801– 1870) and William Fox Talbot (1800 – 1877), used gallic acid for developing latent images in calotypes. It has also been used as a coating agent in zincography.

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SMILES
OC(=O)c1cc(O)c(O)c(O)c1
LogP
0.7 · 0.7
CAS Datenbank
149 · 149-91-7(CAS DataBase Reference)
NIST chemische Informationen
3 · Benzoic acid, 3,4,5-trihydroxy-(149-91-7)
EPA chemische Informationen
Gallic acid (149-91-7)

Verwendengallic acid is a potential bleaching agent and anti-oxidant, it is also astringent and potentially anti-microbial and anti-fungal. Scientists are finding that gallic acid may serve as a skin-lightening agent by inhibiting the action of the tyrosinase and peroxidase enzymes. Some studies indicate that it is more effective than hydroquinone when combined with the proper ingredients. It is also incorporated into anti-aging formulations for its ability to prevent mucopolysaccaride deterioration. It is a constituent of witch hazel and oak bark, among many other plants; however, it is generally obtained from nutgalls for commercial purposes.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

TannineGallnut tanninMelaphis paitan tsai et tangGallic acid monohydrateRhaponticin 6''-O-gallate

Nachgelagerte Produkte

Methyl-3,4,5-trihydroxybenzoatink2,3,4-TrihydroxybenzaldehydEthyl-3,4,5-trihydroxybenzoat1,2,3-Trimethoxybenzol3,4,5-Triethoxybenzoesure2,3,4-Trimethoxybenzaldehyd3,4,5-Trimethoxy benzoic acidProcyanidin B1(4'-O-methyl)methyl gallate5-Bromomethyl-1,2,3-trimethoxy-benzeneOctyl-3,4,5-trihydroxybenzoatMethyl 4,5-dimethoxy-3-hydroxybenzoate3',4',5',6'-Tetrahydroxyspiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-onC.I. Mordant Violet 35 (8CI)1,2,3-TrihydroxyanthrachinonMordant Violet 55
Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: Gallic acid is a trihydroxybenzoic acid in which the hydroxy groups are at positions 3, 4, and 5. It has a role as an astringent, a cyclooxygenase 2 inhibitor, a plant metabolite, an antioxidant, an antineoplastic agent, a human xenobiotic metabolite, an EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor, an apoptosis inducer and a geroprotector. It is a conjugate acid of a gallate.