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5424-20-4

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5424-20-4 Usage

Description

Gallotannin is a polyphenol of gallic acid that has been found in various plants and has antioxidant, anti-inflammatory, antiviral, and antiproliferative biological activities. Gallotannin (1 μM) inhibits the intracellular production of reactive oxygen species (ROS) and DNA damage induced by phorbol 12-myristate 13-acetate (TPA; ) in human polymorphonuclear neutrophils (PMNs). It also decreases TPA-induced nitric oxide release by 90% from primary rat hepatocytes when used at a concentration of 0.5 mM. Gallotannin inhibits hepatitis C virus (HCV) entry into Huh7.5 human hepatoma cells (IC50 = 5.8 μM) and inhibits the proliferation of MDA-MB-231 and MCF-7 human breast cancer cells (IC50s = 2.5 and 4 μM, respectively). In a rat model of middle cerebral artery occlusion (MCAO), it increases superoxide dismutase (SOD1) protein levels and decreases the amount of proteins modified by malondialdehyde (MDA) in ischemic brain tissue when administered at a dose of 10 mg/kg.

Definition

Different sources of media describe the Definition of 5424-20-4 differently. You can refer to the following data:
1. Any of several yellow organic compounds found in vegetable sources such as bark of trees, oak galls, and tea. They are used in tanning animal skins to make leather and as mordants in dyeing. Tannic acid (a type of tannin) is a white solid heterocyclic organic acid extracted from oak galls and used for making dyes and inks.
2. tannin: One of a group of complexorganic chemicals (see depsides) commonlyfound in leaves, unripe fruits,and the bark of trees. Their functionis uncertain though the unpleasanttaste may discourage grazing animals.Some tannins have commercialuses, notably in the production ofleather and ink.

Check Digit Verification of cas no

The CAS Registry Mumber 5424-20-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5424-20:
(6*5)+(5*4)+(4*2)+(3*4)+(2*2)+(1*0)=74
74 % 10 = 4
So 5424-20-4 is a valid CAS Registry Number.
InChI:InChI=1/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

5424-20-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name TANNIC ACID

1.2 Other means of identification

Product number -
Other names Quebracho extract

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5424-20-4 SDS

5424-20-4Synthetic route

tannic acid
5424-20-4

tannic acid

levomethorphan
125-70-2

levomethorphan

dextromethorphan tannate

dextromethorphan tannate

Conditions
ConditionsYield
at 140 - 150℃; for 2h; Neat (no solvent);97%
guaifenesin
93-14-1

guaifenesin

tannic acid
5424-20-4

tannic acid

guaifenesin tannate

guaifenesin tannate

Conditions
ConditionsYield
In water at 35 - 50℃; for 1h; Product distribution / selectivity;96.15%
tannic acid
5424-20-4

tannic acid

levomethorphan
125-70-2

levomethorphan

dextromethorphan tannate

dextromethorphan tannate

Conditions
ConditionsYield
Stage #1: tannic acid In water at 85 - 100℃; for 0.166667h;
Stage #2: levomethorphan In water at 85 - 100℃; for 1.25h;
95.6%
glatiramer acetate

glatiramer acetate

tannic acid
5424-20-4

tannic acid

glatiramer tannate

glatiramer tannate

Conditions
ConditionsYield
In hexane for 2h; Product distribution / selectivity;90%
In methanol for 0.25h; Product distribution / selectivity;76%
With sodium chloride In water for 0.166667 - 2.25h; pH=3.2 - 5.5; Product distribution / selectivity;70%
In water pH=3.2 - 5.5; Product distribution / selectivity;
tannic acid
5424-20-4

tannic acid

D,L-histidine
71-00-1

D,L-histidine

C76H52O46*5C6H9N3O2

C76H52O46*5C6H9N3O2

Conditions
ConditionsYield
In water at 60℃; for 5h; pH=6; Temperature;86.35%
tannic acid
5424-20-4

tannic acid

levomethorphan
125-70-2

levomethorphan

D-M Tannate synthesized by IPA route

D-M Tannate synthesized by IPA route

Conditions
ConditionsYield
Stage #1: tannic acid In isopropyl alcohol at 40 - 45℃; for 1h;
Stage #2: levomethorphan In isopropyl alcohol at 45 - 50℃; for 1h;
83.6%
2-chloroethyl isothiocyanate
1943-83-5

2-chloroethyl isothiocyanate

tannic acid
5424-20-4

tannic acid

C103H88Cl9N9O55

C103H88Cl9N9O55

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 50℃; for 10h; Inert atmosphere;
2-chloroethyl isothiocyanate
1943-83-5

2-chloroethyl isothiocyanate

tannic acid
5424-20-4

tannic acid

C79H56ClNO47

C79H56ClNO47

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 60℃; for 5h; Inert atmosphere;
2-Isocyanatoethyl methacrylate
30674-80-7

2-Isocyanatoethyl methacrylate

p-cyanophenyl isocyanate
40465-45-0

p-cyanophenyl isocyanate

tannic acid
5424-20-4

tannic acid

C151H117N15O66

C151H117N15O66

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 50℃; for 10h; Inert atmosphere;
Tosyl isocyanate
4083-64-1

Tosyl isocyanate

tannic acid
5424-20-4

tannic acid

C116H87N5O61S5

C116H87N5O61S5

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 50℃; Inert atmosphere;
C17H25N5O3

C17H25N5O3

C17H25N5O3

C17H25N5O3

tannic acid
5424-20-4

tannic acid

C110H102N10O52

C110H102N10O52

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 50℃; Inert atmosphere;
2-Isocyanatoethyl methacrylate
30674-80-7

2-Isocyanatoethyl methacrylate

tannic acid
5424-20-4

tannic acid

C146H142N10O76

C146H142N10O76

Conditions
ConditionsYield
With dibutyltin dilaurate In dioxolane, 1,3- at 50℃; for 30h; Inert atmosphere;
N-methoxymethyl-(1-methyl-2-(2-chloroethyl)amino)-ethylamide

N-methoxymethyl-(1-methyl-2-(2-chloroethyl)amino)-ethylamide

tannic acid
5424-20-4

tannic acid

C156H212N20O66

C156H212N20O66

Conditions
ConditionsYield
Stage #1: tannic acid With sodium hydride In N,N-dimethyl acetamide for 3h; Inert atmosphere;
Stage #2: N-methoxymethyl-(1-methyl-2-(2-chloroethyl)amino)-ethylamide In N,N-dimethyl acetamide at 50℃; for 10h; Inert atmosphere;
propan-1-ol
71-23-8

propan-1-ol

tannic acid
5424-20-4

tannic acid

Propyl gallate
121-79-9

Propyl gallate

Conditions
ConditionsYield
With bio-imprinted tannase immobilized on ceolite In hexane; water at 40℃; for 24h; Enzymatic reaction;
With tannase from Aspergillus oryzae In hexane; water at 40℃; Kinetics; Microbiological reaction; Enzymatic reaction;
Stage #1: tannic acid With Aspergillus oryzae tannase at 20℃; for 0.0833333h; pH=6.0;
Stage #2: propan-1-ol With D-Mannose; magnesium sulfate In hexane at 40℃; for 24h; Catalytic behavior; Reagent/catalyst; Enzymatic reaction;
With immobilized tannase In hexane; water at 40℃; for 24h; Solvent;
tannic acid
5424-20-4

tannic acid

3,4,5-trihydroxybenzoic acid
149-91-7

3,4,5-trihydroxybenzoic acid

Conditions
ConditionsYield
With recombinant Tan410 In aq. phosphate buffer at 35℃; for 0.75h; pH=7; Enzymatic reaction;
With ammonium nitrate; dipotassium hydrogenphosphate; potassium dihydrogenphosphate; magnesium sulfate In water at 35℃; for 39h; Microbiological reaction;
4-amino-benzoic acid
150-13-0

4-amino-benzoic acid

tannic acid
5424-20-4

tannic acid

C160H112N12O58

C160H112N12O58

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 120℃; for 24h; Inert atmosphere;
tannic acid
5424-20-4

tannic acid

ellagic acid
476-66-4

ellagic acid

Conditions
ConditionsYield
With sodium hydroxide at 85 - 90℃; for 1h; Concentration; Temperature; Sonication;1.8 g
dodecyl bromoacetate
3674-07-5

dodecyl bromoacetate

tannic acid
5424-20-4

tannic acid

C90H75O48(3-)*3K(1+)

C90H75O48(3-)*3K(1+)

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20 - 25℃; for 5h;
tannic acid
5424-20-4

tannic acid

levomethorphan
125-70-2

levomethorphan

dextromethorphan tannate

dextromethorphan tannate

Conditions
ConditionsYield
In water at 90℃;

5424-20-4Upstream product

5424-20-4Relevant articles and documents

Complexating systems, intermediates for their production and method for obtaining and using the same

-

, (2008/06/13)

The present invention is related to a complexating system comprising a tannin immobilised on a solid support by means of a bifunctional spacer which is covalently bound from one hand to said solid support by a first function and from the other hand to said tannin by a second function, wherein the tannin is a naturally occurring tannin and exhibits at least six hydroxyl groups. Said complexating system can be used in particular for chelating metals and proteins, as an antioxidant, as a radical scavenger or as an antibacterial. More specifically, applications can be found in the clarification and stabilisation of beverages, the treatment of textiles, or the separation and/or purification of proteins and/or metals.

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