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Application Area
Environmental
Environmental

Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.

Clinical diagnostic
Clinical diagnostic

In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.

Organic Chemistry
Organic Chemistry

Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.

Metabolic Research
Metabolic Research

Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.

2,5-Dihydroxybenzoic Acid-[d3]

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General Information
Catalog: BLP-010332
CAS: 294661-02-2
Molecular Formula: C7H3D3O4
Molecular Weight: 157.14
Chemical Structure
2,5-Dihydroxybenzoic Acid-[d3]
Description Labelled 2,6-Difluorophenylboronic acid. 2,5-Dihydroxybenzoic Acid is an active metabolite of salicylic acid degradation. Evidence indicates that gentisic acid has anti-inflammatory, antirheumatic and antioxidant properties. It is also a byproduct of both tyrosine and benzoate metabolisms.
Synonyms 5-Hydroxysalicylic Acid-d3; Carboxyhydroquinone-d3; Gensigen-d3; Gensigon-d3; Gentisinic Acid-d3; Hydroquinonecarboxylic Acid-d3
IUPAC Name 2,4,5-trideuterio-3,6-dihydroxybenzoic acid
Related CAS 490-79-9 (unlabelled)
Isomeric SMILES [2H]C1=C(C(=C(C(=C1O)[2H])C(=O)O)O)[2H]
Canonical SMILES C1=CC(=C(C=C1O)C(=O)O)O
InChI InChI=1S/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11)/i1D,2D,3D
InChI Key WXTMDXOMEHJXQO-CBYSEHNBSA-N
Melting Point >173°C (dec.)
Solubility Soluble in DMSO (Slightly), Methanol (Slightly)
Appearance Brown to Dark Brown Solid
Application An active metabolite of salicylic acid degradation. Evidence indicates that gentisic acid has anti-inflammatory, antirheumatic and antioxidant properties. It is also a byproduct of both tyrosine and benzoate metabolisms.
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