D109606
2,6-Dihydroxybenzoic acid
98%
Synonym(s):
γ-Resorcylic acid
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All Photos(3)
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
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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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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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Tsuyoshi Matsui et al.
Applied microbiology and biotechnology, 73(1), 95-102 (2006-05-10)
We found a bacterium, Pandoraea sp. 12B-2, of which whole cells catalyzed not only the decarboxylation of 2,6-dihydroxybenzoate but also the regioselective carboxylation of 1,3-dihydroxybenzene to 2,6-dihydroxybenzoate. The whole cells of Pandoraea sp. 12B-2 also catalyzed the regioselective carboxylation of
Xiaoxing Wu et al.
Angewandte Chemie (International ed. in English), 48(7), 1283-1286 (2009-01-14)
An extremophilic challenge: Stereospecific condensation of a fully functionalized ketal aldehyde and a 2,6-dihydroxybenzoic acid is the key step in the synthesis of (-)-berkelic acid confirming Fürstner's reassignment of the stereochemistry at C18 and C19, establishing the absolute stereochemistry, and
Masahiro Yoshida et al.
Journal of bacteriology, 186(20), 6855-6863 (2004-10-07)
We found the occurrence of thermophilic reversible gamma-resorcylate decarboxylase (gamma-RDC) in the cell extract of a bacterium isolated from natural water, Rhizobium sp. strain MTP-10005, and purified the enzyme to homogeneity. The molecular mass of the enzyme was determined to
Yukiko Takenaka et al.
Phytochemistry, 72(11-12), 1431-1435 (2011-05-27)
Spore-derived mycobionts of the lichen Graphis proserpens were cultivated on a malt-yeast extract medium supplemented with 10% sucrose and their metabolites were investigated. Isocoumarin derivatives 1-3 and 7-oxo-5,7-dihydrooxepino[4,3,2-de]isochromene derivatives, proserins A-C (4-6), were isolated along with three known isocoumarin derivatives
Tugce Katipoglu et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 45(7), 875-882 (2010-04-27)
The study evaluated the response of an enriched microbial culture on 2,6-dihydroxybenxoic acid (2,6-DHBA) and peptone mixture at low sludge age (theta(X)) under aerobic conditions. It emphasized the effect of culture history by comparing the response of the microbial culture
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