Tannic acid - PharmPure™, USP , CAS No.1401-55-4

Name: Tannic acid - PharmPure™, USP , CAS No.1401-55-4
Brand: Aladdin Scientific
SKU: T292288
Availability: InStock

CAS: 1401-55-4 Cat. No.: T292288 Summenformel: C₇₆H₅₂O₄₆ Molekulargewicht: 1701.20 Beilstein Registry Number: 8186396 EG-Nummer: 215-753-2

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Synonyms

Gallotannin | TANNIC ACID | CAS-1401-55-4 | CHEBI:81066 | HMS3295C21 | A901485 | Tox21_111422 | (2R,3R,4S,5R,6S)-4,5,6-tris({3,4-dihydroxy-5-[(3,4,5-trihydroxyphenyl)carbonyloxy]phenyl}carbonyloxy)-2-[({3,4-dihydroxy-5-[(3,4,5-trihydroxyphenyl)carbonyloxy

Storage

Room temperature,Argon charged

Shipped In

Normal

Übersicht Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Warum diese Qualität

PharmPure™, USP PharmPure™,USP für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Room temperature,Argon charged Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 1402 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Product Introduction

Slightly special smell, strong astringency, exposure to light and deep color change in the air. Soluble in water, easily soluble in ethanol, acetone and glycerol, almost insoluble in ether, benzene, chloroform and petroleum ether. Slightly special smell and strong astringency.

Pale yellow amorphous powder or loose shiny scaly or spongy solid, which is mostly decomposed into pyrogallic acid and carbon dioxide at 210-215℃. 1g is dissolved in 0.35ml water and 1ml hot glycerin. It is odorless and flammable. When exposed to albumin, starch, gelatin, and many alkaloids and metal salts, they precipitate, and when exposed to iron salts, they also produce black or precipitate. Autoignition point 526.6℃; The median lethal dose (LD) (rabbit, oral) was 5.0g/kg.

Tannin is not a single compound, but its chemical composition is complex and can be roughly divided into two types:

(1) condensed tannin is flavanol, and the 2-position of flavanol in the molecule is combined with catechol or phloroglucinol through carbon-carbon bond.

② Hydrolyzable tannin, with ester bond in its molecule, is gallic acid ester of glucose. The latter is commonly used tannin. Tannin from Chinese gallnut contains about 12% glucose, and tannin from Turkish gallnut contains about 16.5% glucose.

Product Usage

Precipitation and gravimetric determination of beryllium, aluminum, gallium, indium, niobium, tantalum and zirconium. Comparative determination of copper, iron, vanadium, cerium and cobalt. Precipitators for proteins and alkaloids. External indicator for titration of lead with ammonium molybdate. Dye mordant.

Iron tannin complex was synthesized by reaction with metallic iron. Deproteins in the preparation of genome and plasmid DNA. As a reducing agent in the synthesis of metal nanoparticles.

Spezifikationen

Synonyme

Spezifikationen & Reinheit

PharmPure™, USP

Storage

Room temperature,Argon charged

Verschickt in

Normal

Note

PharmPure™, USP

Namen und Kennungen

Kanonisches Lächeln

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

IUPAC Name

[2,3-dihydroxy-5-[[(2R,3R,4S,5R,6S)-3,4,5,6-tetrakis[[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy]oxan-2-yl]methoxycarbonyl]phenyl] 3,4,5-trihydroxybenzoate

InChIKey

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

Isomere SMILES

C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OC[C@@H]3[C@H]([C@@H]([C@H]([C@@H](O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O

WGK Deutschland

RTECS

WW5075000

Alternative CAS-Nummer

5424-20-4

Molekulargewicht

1701.20

Beilstein

8186396

Dokumentation

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Klasse Tannins
    - Subclass Hydrolyzable tannins

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Klasse	Tannins
Subclass	Hydrolyzable tannins
Intermediate Tree Nodes	Not available
Direct Parent	Hydrolyzable tannins
Alternative Parents	Depsides and depsidones Galloyl esters p-Hydroxybenzoic acid alkyl esters m-Hydroxybenzoic acid esters Phenol esters Pyrogallols and derivatives Phenoxy compounds Benzoyl derivatives Catechols 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Monosaccharides Carboxylic acid esters Oxacyclic compounds Acetals Polyols Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Hydrolyzable tannin - Depside backbone - Galloyl ester - Gallic acid or derivatives - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Dihydroxybenzoic acid - Phenol ester - Benzoate ester - Benzenetriol - Benzoic acid or derivatives - Pyrogallol derivative - Phenoxy compound - Catechol - Benzoyl - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Oxane - Benzenoid - Monocyclic benzene moiety - Carboxylic acid ester - Polyol - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.
External Descriptors	tannin
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

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CYP1A2 Tchem Cytochrome P450 1A2 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

FYN Tclin Tyrosine-protein kinase Fyn (1 Activities)

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TBXAS1 Tchem Thromboxane-A synthase (1 Activities)

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PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

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HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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CALCR Tclin Calcitonin receptor (2215 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH1 Tclin Histamine H1 receptor (7573 Activities)

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ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

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ESR2 Tclin Estrogen receptor beta (9272 Activities)

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CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

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ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)

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CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)

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CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)

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ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)

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pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)

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Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

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ampC Beta-lactamase AmpC (62480 Activities)

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Ltc4s Leukotriene C4 synthase (1 Activities)

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Sigmar1 Sigma opioid receptor (160 Activities)

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Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Mapk1 MAP kinase ERK2 (650 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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Carbonic anhydrase (69 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Salmonella typhimurium (15756 Activities)

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Staphylococcus aureus (210822 Activities)

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Plasmodium falciparum (966862 Activities)

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Caenorhabditis elegans (1055 Activities)

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Rattus norvegicus (775804 Activities)

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Dengue virus type 2 NS3 protein (2214 Activities)

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GCN5 Histone acetyltransferase GCN5 (89 Activities)

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Luciferin 4-monooxygenase (66902 Activities)

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pfk 6-phospho-1-fructokinase (7870 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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TGR Thioredoxin glutathione reductase (28579 Activities)

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Large T antigen (1457 Activities)

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CCT2 T-complex protein 1 subunit beta (5007 Activities)

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Glra2 Glycine receptor (1745 Activities)

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groL GroEL/GroES (1042 Activities)

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groEL 60 kDa chaperonin (64 Activities)

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Wirkungsmechanismen

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20 results found

Lot Number	Certificate Type	Datum	Artikel
A2306154	Certificate of Analysis	Sep 22, 2026	T292288
G2629672	Certificate of Analysis	Jul 13, 2026	T292288
G2629670	Certificate of Analysis	Jul 13, 2026	T292288
L2529003	Certificate of Analysis	Nov 24, 2025	T292288
L2529002	Certificate of Analysis	Nov 24, 2025	T292288
A2605657	Certificate of Analysis	Nov 24, 2025	T292288
F2518552	Certificate of Analysis	Jun 06, 2025	T292288
F2518557	Certificate of Analysis	Jun 06, 2025	T292288
L2410715	Certificate of Analysis	Nov 22, 2024	T292288
L2416398	Certificate of Analysis	Nov 22, 2024	T292288
H2428357	Certificate of Analysis	Aug 02, 2024	T292288
H2428358	Certificate of Analysis	Aug 02, 2024	T292288
B23271229	Certificate of Analysis	Jan 05, 2023	T292288
B2327978	Certificate of Analysis	Jan 05, 2023	T292288
E2429043	Certificate of Analysis	Jan 05, 2023	T292288
B23271076	Certificate of Analysis	Jan 05, 2023	T292288
B23271075	Certificate of Analysis	Jan 05, 2023	T292288
H2222291	Certificate of Analysis	Dec 13, 2021	T292288
K2229678	Certificate of Analysis	Dec 13, 2021	T292288
A2411054	Certificate of Analysis	Dec 13, 2021	T292288

Chemische und physikalische Eigenschaften

Löslichkeit	Soluble in water, warm glycerol, alcohol and acetone.
Empfindlichkeit	Air & Light Sensitive
Flammpunkt (°F)	390.2 °F
Flammpunkt (°C)	199 °C
Schmelzpunkt (°C)	210-215°C
Molekulargewicht	1701.200 g/mol
XLogP3	6.200
Hydrogen Bond Donor Count	25
Hydrogen Bond Acceptor Count	46
Rotatable Bond Count	31
Exact Mass	1700.17 Da
Monoisotopic Mass	1700.17 Da
Topological Polar Surface Area	778.000 Å²
Heavy Atom Count	122
Formal Charge	0
Complexity	3570.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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Tannic acid - PharmPure™, USP , CAS No.1401-55-4

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Tannic acid - PharmPure™, USP , CAS No.1401-55-4

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