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%
Synonym(s):
γ-Resorcylic acid
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D109606-25G
$40.12
D109606-100G
$61.70
About This Item
Linear Formula:
(HO)2C6H3CO2H
CAS Number:
Molecular Weight:
154.12
Beilstein/REAXYS Number:
2209755
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
1 of 4
This Item | D109401 | D110000 | D804 |
|---|---|---|---|
| assay 98% | assay 97% | assay 97% | assay 98% |
| Quality Level 200 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| mp 165 °C (dec.) (lit.) | mp 208-211 °C (dec.) (lit.) | mp 236-238 °C (dec.) (lit.) | mp - |
| form powder | form powder | form powder | form liquid |
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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
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
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
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