Ellagic acid, 98%

cas: 476-66-4 — see every product listed under this CAS number, including other names

Ellagic acid, 98% (CAS 476-66-4) is a chemical reagent available from Chemat. Available pack sizes: 100g, 1g, 5g, 50g, 25g, 10g. Offered by: Chemat.

brandChemat
catalog numberCh114PX0-100g
cas476-66-4
size100g
availability 10000g
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Available pack sizes

brand size price
Chemat 100g 304.40 Pln
Chemat 1g 74.00 Pln
Chemat 5g 78.80 Pln
Chemat 50g 194.00 Pln
Chemat 25g 136.40 Pln
Chemat 10g 93.20 Pln

properties

purity98%
delivery time3 weeks
Structural formula: {0} (CAS {1})

Ellagic acid is an organic heterotetracyclic compound resulting from the formal dimerisation of gallic acid by oxidative aromatic coupling with intramolecular lactonisation of both carboxylic acid groups of the resulting biaryl. It is found in many fruits and vegetables, including raspberries, strawberries, cranberries, and pomegranates. It has a role as an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor, a geroprotector, an antioxidant, an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor, a food additive, an EC 2.5.1.18 (glutathione transferase) inhibitor, a plant metabolite, a fungal metabolite, an EC 2.3.1.5 (arylamine N-acetyltransferase) inhibitor, an EC 2.4.1.1 (glycogen phosphorylase) inhibitor, an EC 2.7.1.127 (inositol-trisphosphate 3-kinase) inhibitor, an EC 2.7.1.151 (inositol-polyphosphate multikinase) inhibitor, an EC 2.7.4.6 (nucleoside-diphosphate kinase) inhibitor and a skin lightening agent. It is a lactone, a polyphenol, a member of catechols, an organic heterotetracyclic compound and a cyclic ketone. It is functionally related to a gallic acid. It is a conjugate acid of an ellagic acid(2-).

Source: ChEBI

Identity
Molecular formulaC14H6O8
Molecular weight302.19 g/mol
IUPAC name6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione
InChIKeyAFSDNFLWKVMVRB-UHFFFAOYSA-N
SMILESC1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O

Computed by PubChem (NCBI)

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