No, the 2,6-dihydroxybenzoic acid is not available in pill/capsule form. Please note this product is intended for research use only. It is not suitable for any other purpose, which includes, but is not limited to, unauthorized commercial use, in vitro diagnostic use, or therapeutic use in humans or animals.
D109606
2,6-Dihydroxybenzoic acid
98%
Synonyme(s) :
γ-Resorcylic acid
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About This Item
Formule linéaire :
(HO)2C6H3CO2H
Numéro CAS:
Poids moléculaire :
154.12
Beilstein:
2209755
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Le tarif et la disponibilité ne sont pas disponibles actuellement.
Produits recommandés
Niveau de qualité
Essai
98%
Forme
powder
Pf
165 °C (dec.) (lit.)
Chaîne SMILES
OC(=O)c1c(O)cccc1O
InChI
1S/C7H6O4/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3,8-9H,(H,10,11)
Clé InChI
AKEUNCKRJATALU-UHFFFAOYSA-N
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Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Les clients ont également consulté
J S Shane Rountree et al.
Organic letters, 11(4), 871-874 (2009-01-28)
The facile preparation of a novel 8-membered polyhydroxylated salicylic acid lactone from 2,6-dihydroxybenzoic acid and sodium thio-D-glucose is described. The key step involved a sodium hydride promoted intramolecular lactonization in the presence of excess TMSCl, which led to isolation of
Derin Orhon et al.
Environmental technology, 33(13-15), 1517-1522 (2012-09-20)
The paper mainly focused on illustrating the merit of respirometric analysis in assessing the inhibitory/toxic impact of xenobiotics on substrate biodegradation. It also evaluated biodegradation characteristics of these chemicals at continuous exposure through acclimation ofthe microbial culture. The nature and
Toyokazu Yoshida et al.
Archives of microbiology, 181(6), 391-397 (2004-05-01)
A nonoxidative decarboxylase, 2,6-dihydroxybenzoate decarboxylase, was found in Agrobacterium tumefaciens IAM12048. The enzyme activity was induced specifically by 2,6-dihydroxybenzoate. The purified enzyme was a homotetramer of identical 38 kDa subunits. The purified decarboxylase catalyzed the nonoxidative decarboxylation of 2,6-dihydroxybenzoate and
Masahiro Yoshida et al.
Journal of bacteriology, 189(5), 1573-1581 (2006-12-13)
We identified a gene cluster that is involved in the gamma-resorcylate (2,6-dihydroxybenzoate) catabolism of the aerobic bacterium Rhizobium sp. strain MTP-10005. The cluster consists of the graRDAFCBEK genes, and graA, graB, graC, and graD were heterologously expressed in Escherichia coli.
Derin Orhon et al.
Bioresource technology, 101(8), 2665-2671 (2009-11-27)
This study investigated the fate of 2,6-dihydroxybenzoic acid in a mixed microbial culture acclimated to peptone under aerobic conditions. A laboratory-scale sequencing batch reactor receiving a pulse feeding of peptone at the start of each daily cycle was used for
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