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D109606

Sigma-Aldrich

2,6-Dihydroxybenzoic acid

98%

Synonym(s):

γ-Resorcylic acid

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About This Item

Linear Formula:
(HO)2C6H3CO2H
CAS Number:
Molecular Weight:
154.12
Beilstein:
2209755
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

powder

mp

165 °C (dec.) (lit.)

SMILES string

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)

InChI key

AKEUNCKRJATALU-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
Emine Ubay Cokgor et al.
Bioresource technology, 102(2), 567-575 (2010-08-24)
This study evaluated the kinetics of simultaneous biodegradation of peptone mixture and 2,6-dihydroxybenzoic acid (2,6-DHBA) by an acclimated dual microbial culture under aerobic conditions. A laboratory-scale sequencing batch reactor was sustained at steady-state with peptone mixture feeding. During the study
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
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
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

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