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Merck

403040

Tannic acid

ACS reagent grade, powder or solid

Synonym(s):

Gallotannin, Tannin

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About This Item

Empirical Formula (Hill Notation):
C76H52O46
CAS Number:
Molecular Weight:
1701.20
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
215-753-2
MDL number:
Beilstein/REAXYS Number:
8186396

Product Name

Tannic acid, ACS reagent

InChI key

LRBQNJMCXXYXIU-PPKXGCFTSA-N

InChI

1S/C76H52O46/c77-32-1-22(2-33(78)53(32)92)67(103)113-47-16-27(11-42(87)58(47)97)66(102)112-21-52-63(119-72(108)28-12-43(88)59(98)48(17-28)114-68(104)23-3-34(79)54(93)35(80)4-23)64(120-73(109)29-13-44(89)60(99)49(18-29)115-69(105)24-5-36(81)55(94)37(82)6-24)65(121-74(110)30-14-45(90)61(100)50(19-30)116-70(106)25-7-38(83)56(95)39(84)8-25)76(118-52)122-75(111)31-15-46(91)62(101)51(20-31)117-71(107)26-9-40(85)57(96)41(86)10-26/h1-20,52,63-65,76-101H,21H2/t52-,63-,64+,65-,76+/m1/s1

SMILES string

Oc1cc(cc(O)c1O)C(=O)Oc2cc(cc(O)c2O)C(=O)OC[C@H]3O[C@@H](OC(=O)c4cc(O)c(O)c(OC(=O)c5cc(O)c(O)c(O)c5)c4)[C@H](OC(=O)c6cc(O)c(O)c(OC(=O)c7cc(O)c(O)c(O)c7)c6)[C@@H](OC(=O)c8cc(O)c(O)c(OC(=O)c9cc(O)c(O)c(O)c9)c8)[C@@H]3OC(=O)c%10cc(O)c(O)c(OC(=O)c%11cc(O)c(O)c(O)c%11)c%10

grade

ACS reagent

form

powder or solid

autoignition temp.

980 °F

Quality Level

impurities

≤0.003% Lead

ign. residue

≤0.5%

loss

≤12.0% loss on drying, 105°C

mp

218 °C (lit.)

cation traces

Zn: ≤0.005%
heavy metals: ≤0.003%

functional group

ester
ether

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Application

Tannic acid may be used in the following processes:
  • Synthesis of ferric tannate complexes by reacting with metallic iron.
  • As a protein deproteinizing agent in genomic and plasmid DNAs preparation.
  • As a reductant in the synthesis of metal nano particles.

General description

Tannic acid (TA) is a natural, non-toxic organic acid with corrosion inhibitive property for metals and alloys. A chemiluminescence (CL) system of KIO4 (potassium periodate)–H2O2 (hydrogen peroxide)–Tween40 has been employed in the detection of tannic acid in industrial wastewater. Tannic acid hydrolyzes to form mainly glucose and gallic acid. Its astringent property is due to the presence of polyphenolic groups.

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

390.2 °F

flash_point_c

199 °C

ppe

Eyeshields, Gloves, type N95 (US)


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Reviewing the tannic acid mediated synthesis of metal nanoparticles.
Ahmad T.
Journal of Nanotechnology, 2014 (2014)
Fikret Türkan et al.
Journal of biochemical and molecular toxicology, 33(8), e22340-e22340 (2019-04-12)
Multiple studies have been recorded on the synthesis and design of multi-aim anti-Alzheimer molecules. Using dual butyrylcholinesterase/acetylcholinesterase inhibitor molecules has attracted more interest in the therapy for Alzheimer's disease. In this study, a tannic acid compound showed excellent inhibitory effects
Tannic acid as corrosion inhibitor for metals and alloys.
Kusmierek E and Chrzescijanska E.
Materials and Corrosion, 66(2), 169-174 (2013)
On the tannic acid interaction with metallic iron.
Iglesias J, et al.
Hyperfine Interactions, 134(1), 109-114 (2001)
Deproteinization of bacterial genomic and plasmid DNAs by tannic acid.
van Huynh, N.
Journal of Microbiological Methods, 75(2), 379-381 (2008)

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